Christines Blog (Archive Blogs 1)



Saturday 25th September 2010Grant & Debbie

Here is another letter to join the dozens that David Cameron has received from families who have lost a loved one to vCJD…

Currently these heartfelt and factual requests for justice are being ignored by our PRIME MINSTER and his Government………why?

Cameron likes to appear a new ‘Tory’ and man of the people when in fact Thatcherism its greed and cover-ups perpetuated by cronies such as Kenneth Clarke have a grip on his cabinet and actions….

Shame on David Cameron, this family man who regularly turns his back on vCJD victims plight and their families heartbreak and need for resolution….…..

Even though vCJD regularly maims and kills innocent members of the UK public, David Cameron and his Government do nothing to recognise or address the significant health risk to every member of the UK population. Everyone over 13 including vegetarians have been exposed to at least 50 BSE infected meals and vaccines made from bovine material from infected herds.

DAVID CAMERON has refused to meet with any families who have been affected by vCJD …what is he so afraid of? And who?

3 Copperwood Wynd Hamilton Lanarkshire ML3 0RP

Dear Sir

My name is Thomas Goodwin, on the 16th of January 2009 my son Grant became another victim of BSE.

Grant died the most horrific death from VCJD having suffered two years of hell not knowing what was wrong with him.

There are now over 200 deaths from VCJD; Grant is the first MV gene type to have died of this British manmade disaster which is widely regarded as Britain’s worst food scandal.

It is also widely perceived that the crisis stemmed from serious policy failures, Government secrecy and a conflict of interest in the Ministry of Agriculture, Fisheries and Food.

The two people that I hold responsible for my son’s death are John Gummer who was the Minister of Agriculture, Fisheries and Food, and Kenneth Clark who was the Minister for Health during this crisis who between them decided it was better to cover this up when the first cases of BSE were found in the early 80’s because of the implications it could have had to the Meat industry.

The report into the BSE scandal was carried out by Lord Phillips, Lord Phillips states at the start of his report; it was not the intention to hold anybody accountable but to see what could be learned from this atrocity.

This should have been a criminal investigation into the deaths of over 200 young people and these two people along with many others should have been jailed for a very long time.

The Phillips report did nothing but protect the people that were responsible for the cover up of BSE when it was first was detected in cattle and protected the conservative Government.

The last Government left the country in financial difficulties, the last Conservative Government left the country with BSE and who knows how many deaths from VCJD.

It seems to me that Government Ministers are above the law when it comes to the unlawful Killing of my son Grant, and many others.

Kenneth Clark still sits in Parliament, John Gummer sits in the House of Lords, and still picking up massive salaries, this to me is typical of Government hypocrisy.

It is not worth my while asking to meet with you or any member of the Government, nobody wants to talk about VCJD especially Government Ministers because of the massive cover up operation that has went on in the last 20 years, and still goes on.

Many Powerful people turned a blind eye to BSE, Margaret Thatcher, and John Major just to name a few, who were controlling the Ministers who I hold responsible for my son Grant’s death.

These people will go on to live very long lives because they knew the implications of eating contaminated meat were the British people who put them in power were not given that choice, these people have no conscience, they don’t lose sleep over the deaths of so many young people, but the parents and families of the victims are left to live this nightmare for the rest of their lives.

I will be sending a copy of this letter to Nick Clegg, Kenneth Clark and John Gummer

I look forward to hearing from you regarding the death of my son Grant and who I hold accountable.

Yours Tommy Goodwin


Thursday 23rd September 2010

Below is an article from The Herald published Saturday 18th September 2010, about Plympton vCJD victim John Stringer.

My thoughts and condolences are with John’s family, who is now the oldest person officially to die of vCJD.

John was treated for dementia and his family are stunned to learn that he died of the human form of BSE.

How many other elderly people have been misdiagnosed and buried/cremated who have really died of vCJD?

The reference to Spain is a red herring as it’s more likely that John was infected in the UK. He was also born in Portsmouth.

According to my sources the inquest was short sharp and kept very low key…why?

No representative from the Edinburgh CJD unit appeared or gave evidence. My sources tell me the inquest was unusually short and it felt as
if the authorities wanted to keep it secret so that it wouldn’t cause any public interest or concern.

Experts believe we face an global epidemic of dementia in the next few years this is in direct correlation with BSE exposure…..

My thoughts and prayers are with John’s family at this very sad time…..and I fear Johns death is just the tip of the iceberg of older people who have died and are dying of vCJD…….

Saturday, September 18, 2010, 07:00

Plymouth man John Stringer killed by mad cow disease CJD

By Ed Moore The Herald reporter

A TALENTED squash player from Plympton died after contracting the human form of mad cow disease, an inquest has found.

Grandfather John Stringer, who had played the sport at county level, passed away in May after being struck down by Creutzfeldt–Jakob disease (CJD).

An inquest in Plymouth yesterday revealed to his family for the first time that the incurable brain condition CJD was to blame.

They believe he had eaten infected beef in Spain, a country Mr Stringer, 76, had regularly visited.

The inquest was told how the retired personnel manager was a fit and healthy squash enthusiast until suddenly becoming ill last year.

He began showing signs of dementia — a common symptom in CJD cases — before becoming "extremely unwell" and slipping into a coma.

Mr Stringer was moved from hospital to St Francis Nursing Home in Plymbridge Road, Plympton, on April 20 and passed away on May 8.

Post-mortem examinations showed he died of bronchopneumonia and pulmonary embolism, though the inquest was told how the conditions had been triggered by the human strain of BSE.

BSE — or Bovine Spongiform Encephalopathy — first appeared in British cattle in 1986.

CJD, the human form, is a degenerative neurological condition and there is no cure. Patients usually die within four months of the onset of symptoms.

Details of Mr Stringer's death had been passed to Professor James Ironside, a specialist from the Edinburgh-based UK CJD Surveillance Unit, the inquest was told.

Mr Stringer was born in Portsmouth in July 1933, marrying former midwife Rosemary and settling in Plympton.

Plymouth Coroner Ian Arrow recorded that he died of natural causes, and told his family they had no reason to be concerned for their own health.

Summing up, he said: "At the time of John's death, it was unknown why he died.

"I feel very sorry for the family that John died so suddenly."


Monday 20th September 2010St Andrews in Northern Cyprus

I have just returned to the UK from a trip which included a visit to Northern Cyprus, my time in this part of the world was very helpful.

Turkish Muslims, Greeks and nationalities from all faiths and ethnicities have died of vCJD.

Whilst in Cyprus I visited the Karpaz peninsula and spent time at the shrine of Saint Andrew (Andreas Aposotolos) and met the monastery’s one remaining monk a 75 year old who lives alone at the top of a mountain. (See photo)

Surrounded by ancient icons and with a sense of serenity I lit a candle for my Andrew and all victims of vCJD. Whenever I visit a place of worship I am surrounded by the belief that the soul never dies and that my Andrew is just a heartbeat away from my arms.

Whilst lighting the candle and spending time in peaceful reflection, I also repeated my vow to continue to be the voice of my Andrew and all victims of vCJD.

Muslims, Sikhs, Hindus, Jews, Catholics, Protestants, Buddhist, and people from all religious beliefs and faiths have died or been affected by vCJD.

This horrific man made disease crosses all religious, cultural barriers uniting our global family in a strong alliance to reach for the truth and justice.

Whenever I enter a mosque, church, temple, synagogue, cathedral or religious building I always say a few words for all those who have died and continue to suffer. When I lit the candle at St Andrews Monastery it was also to light the way forward for all the families across the globe that has formed a multi faith and cultural alliance with the campaign.

Thank you all for your continued support and information….

May your god be with you all…..


Wednesday 15th September 2010Emma, Andrew & Christine

INFORMATION ABOUT VACCINES

www.vaccineriskawareness.com

Glaxo still make vaccines with thimerosal, a 49% mercury compound. It is present in their recently invented H1N1 jab that was given to pregnant mothers.

Thimerosal is also used in other flu jabs and it is used in the manufacturing process of all vaccines, just not as an added ingredient, so it will be in vaccines labelled mercury free in quantities of less than 3mcgs per shot.

This is what it says for pandemrix H1N1 flu vaccine:

After mixing, 1 dose (0.5 ml) contains:
Split influenza virus, inactivated, containing antigen* equivalent to:
A/California/07/2009 (H1N1) derived strain used NYMC X-179A 3.75 micrograms**
* propagated in eggs
** haemagglutinin
AS03 adjuvant composed of squalene (10.69 milligrams), DL-α-tocopherol (11.86 milligrams) and polysorbate 80 (4.86 milligrams)
The suspension and emulsion, once mixed, form a multidose vaccine in a vial. See section 6.5 for the number of doses per vial.
Excipients: the vaccine contains 5 micrograms thiomersal.

So it has 5 mcgs of thimerosal (mercury), polysorbate 80 (which causes infertility in animals) and squalene which is shark liver oil, deeply immuno-reactive and linked to Gulf war syndrome and arthritis.

Here is the link:
http://www.medicines.org.uk/EMC/medicine/22352/SPC/Pandemrix+suspension+and+emulsion+for+emulsion+for+injection/#COMPOSITION

If you want to know any ingredients, side-effects of vaccines just go to this site (emc medicines) and type in the brand name of the drug or vaccine you are interested in and it will bring up the data sheet.

Here is a link to the CDC pink book which lists vaccine ingredients, including bovine serum. Although US vaccines differ slightly in composition, the situation is similar in the UK:

http://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/b/excipient-table-2.pdf

Other nasties to look out for in vaccines include octoxynol 9 and 10 (spermicide), aluminium, formaldehyde (known throat cancer agent and used to embalm bodies), phenoxyethanol (phenol is the main ingredient of anti-freeze), sodium borate (ant powder), human diploid cell (tissue from aborted human babies) and of course any vaccine that contains gelatine may in fact have bovine material in it depending on what animal the gelatine came from. For instance, MMR contains gelatine. It also contains chick embryo, human diploid cells, phenols and other things.

http://www.medicines.org.uk/EMC/medicine/20968/SPC/MMRVAXPRO/#COMPOSITION
www.vaccineriskawareness.com


Tuesday 14th September 2010Andrews Last Days

The articles below were written in 1999 and highlights just how much scientific knowledge was available regarding the toxicity of BSE. As early as 1988 there were severe concerns that were officially recorded in Whitehall, regarding vaccines and contamination with BSE infected material. Why could the Chief Medical Officer Donald Acheson be allowed to let these deadly vaccines continue in the assumption he ‘suspected there was no risk?’ but it would take ‘ 30 or 40 years to prove’……how appalling that our children’s and babies lives were played with Russian roulette style…

.Donald Acheson died this year in his bed an old man of eighty….my son died aged 24 of vCJD because of Achesons lies and cover-ups…..

The UK publics health was never a priority and the risk not deemed important, ( after all what was one or two lives lost?) This is how the likes of Acheson, Thatcher, Gummer, Clarke and their cronies played out the BSE scandal….

One life lost is one too many if its avoidable…and hundreds so far have died and thousands more have been affected by the shadow of vCJD.

How would they feel if it was their child or loved one?

The huge profits that were being made in the 1980s and 1990s by the drug and agriculture corporations were paramount. Government policy backed making money for business at the expense of our families health and futures……

This resulted in contaminated vaccines being given to millions of UK babies and children. As one medic who works at the Prion Unit in Queens Square, London,

Said to me ‘It’s terrible that what you thought would be good for Andrew killed him.’ When this expert pressed wouldn’t elaborate…..

My Andrew was just 5 years old…in 1988 …if all vaccines had been destroyed then and no bovine material used ….maybe he might still be alive…..? and perhaps all the other young victims of vcjd might be alive too?

http://www.whale.to/vaccines/bse.htm

VACCINE AND NOT HEARD Paul Foot, Private Eye 19 Feb, 1999

THOUGH hearings at the Phillips public inquiry into BSE have broken up for a few weeks, its officials are drawing up what may turn out to be their most controversial document. It is a draft factual account of government policy on vaccines prepared for injection into masses of people, almost all of which contain some material derived from beef.

The first hint that anyone in officialdom was worried about the impact of BSE on these vaccines came at a meeting of senior officials at the department of health on 17 March 1988.

The feeling of the meeting was summed up by ministry of agriculture under secretary Alistair Cruikshank, as follows: "there is probably no risk in drinking milk or eating flesh from animals affected by BSE, but that the position was much less clear in relation to brains, spleens and other organs. This raised questions about the safety of human vaccines prepared using bovine material."

The chief medical officer Sir Donald Acheson said he suspected there was no risk, but this could take "30 to 40 years to prove". In the meantime, he warned, "ministers would be very exposed, if, as seems inevitable, the press began to devote attention to the subject".

The press showed no interest. But others were worried. A memo from Dr Hilary Pickles at the department of health on 21 June 1988 revealed: "I understand the pharmaceutical industry are also concerned: they had been using bovine not sheep products in various processes because scrapie is endemic in British sheep... the highest risk would be from parenterals [for injection] prepared from brain [eg rabies vaccine]."

The BSE scare led to the appointment of an expert committee of inquiry under Oxford zoology professor Sir Richard Southwood. On 30 August 1988 Sir Richard wrote to Acheson: "The only outstanding practical matter that we need to address at the present time is the use of serum in pharmacological work. I heard... that Wellcome are now only using serum from New Zealand."

Wellcome's initiative in getting its vaccine beef products from herds in New Zealand, which had not been fed on animal products as in Britain, was not yet insisted on by the government. Three times in 1988, Sir Richard Southwood wrote to the relevant statutory body, the Committee on Safety of Medicines, which is made up of top medical experts, many of whom are linked to the drug companies, asking for more urgent action on vaccines.

On 16 December 1988 a meeting of the Southwood committee considered that the response from the safety of medicines committee "was somewhat complacent, particularly in relation to the problem of existing medicinal products". On 26 January 1989, the Committee on Safety of Medicines wrote to Southwood that guidelines for the industry had been agreed. In future, bovine serum should only be taken from "appropriately certified herds".

The committee's letter went on: "Many vaccines are stored for up to five years before being released and this will therefore have to be considered."

The Southwood committee report was published the following month, February 1989. "The greatest risk in theory" it warned, "would be from parenteral injection of material derived from bovine brain or lymphoid tissue. Medicinal products for injection which are prepared from bovine tissues... might also be capable of transmitting infectious agents."

Prompted by the report, the Committee on Safety of Medicines sent 4,000 letters to drug companies asking for information about bovine products. Not all the information from these letters was passed on to the authorities. Sir Donald Acheson, chief medical officer, told the recent Phillips inquiry: "We were told that a number of things that we wanted to discuss were confidential in the commercial sense... and that they could not discuss them with us... They put up with me, but every now and again they would say 'Sorry we cannot share that with you'."

Nor was the information always accurate. A memo from the committee in September 1988 revealed: "The computer list show's 33 product licences extant for preparations of bovine origin." The memo categorically asserted:

"There are no licensed products derived from bovine brain." At the recent inquiry, Sir Donald was asked:

Q: Would you have been concerned if there were licensed products from

bovine brain?

A: Surely

Q: I want you to look at an extract from the MCA questionnaire summary.. One of the items is under a company number - we have 01234, because it is not right that the company should be identified here.

Company name, a large company. The product name is drug X. Animal specification is bovine and the animal ingredients include calf brain.

Do you see that?

A: I do.

Q: If you had known about that at the time, would that have caused you concern?

A: It certainly would, unquestionably, which I did not.

After some delay the Committee on Safety of Medicines guidelines ensured that the drug companies got their bovine materials from "healthy herds" in Australia and New Zealand. But what happened to all those vaccines with bovine material from unhealthy British herds, which were stored up sometimes five years in advance? On 31 October 1990, the committee's BSE working group minutes recorded: VACCINE STOCKS. Dr David Taylor declared a non-specific non personal interest in (company name deleted) and took part in the discussion. Dr Richard Kimberlin declared a specific personal interest and did not participate in the discussion but remained at the meeting.

"The working group considered that the secretariat should explore with the company the possibility that the unabsorbed vaccines which had limited usage should be replaced with batches using bovine materials which complied with the guidelines, especially where the stock-out date extended beyond 1991. There may be some commercial loss to the licence holder but it is unlikely to be very large." A list of the relevant vaccines was attached.

What happened then? What happened to the stored vaccines which, if injected into people, might carry the danger of infection? No one seems to know. The former Tory ministers who gave evidence to the Phillips inquiry didn't know. Asked about vaccines, they responded as follows: William Waldegrave: "I do not remember that as an issue."

John Macgregor: "I cannot remember, frankly.." Tony Newton: "I do not think I am in a position to help you." Edwina Currie: "I have not refreshed my memory.. Had the experts said: 'We feel the vaccines being built up are not entirely free of risk, we are therefore going to recommend that they be destroyed and that replacement stocks are acquired, and that this may delay the onset of the (immunisation) campaign for two weeks', we would have said: 'fine'." Kenneth Clarke, who was secretary of state for health from 1988 to 1990: "What one clearly got from all this was that they were advising us that we should continue with vaccine components and so on and the risk was so remote that [it] would not justify stopping it. I still believe that advice to have been correct."

The Eye asked the BSE inquiry, which has heard 300 witnesses, what information has come to light which reveals what happened to the stocks of vaccines with bovine serum from British cows manufactured before the BSE scare broke. A spokeswoman replied: "We have no information which can answer any of those questions."

The Eye put the same questions to the department of health. "We outsourced the supplies of bovine material for vaccines away from Britain very early," said a spokeswoman. In reply to the question "when were the old stocks replaced?", the department sent a 16 page calendar of events, which reveals:

• As late as July 1992: "The Group's previous concern about vaccine stocks in relation to a specific company [unnamed] were resolved by the company concerned producing a new batch with New Zealand foetal calf serum of assured quality."

• Not until November 1996: "All currently licensed vaccines complied with the guidelines and did not contain any UK-sourced bovine material." Neither item, nor any other in the 16 pages, answered the question. Vaccine to be done? (Private Eye, Aug 1999)

The sensitive and unresolved issue of the possible contamination of vaccines by bovine products affected by BSE (see Eye 970) came up again at the Phillips inquiry into BSE on July 21.

Four of the country’s top scientists, the members of the Southwood inquiry into BSE in the late l980s, gave evidence. They were Sir Richard Southwood, Professor of Zoology and Pro Vice Chancellor at Oxford University; Lord Walton, a world-famous clinical neurogist and former president of the General Medical Council; Sir Anthony Epstein, a former head of the department of pathology at Bristol and Dr A.W. Martin, a distinguished vet who had just retired as director of the Moredun research institute in Edinburgh. All four were given a torrid time by the counsel to the inquiry, Paul Walker, on the subject of the vaccines.

He wanted to know whether the Southwood committee report had given a "misleading picture" of the dangers to humans from widely-used vaccines, almost all of which contained bovine material, much of it from cattle infected by BSE. The committee had described such dangers as ‘remote" — exactly the same adjective they had used to describe the dangers of people catching BSE or associated diseases from eating BSE-infected meat. Close questioning of the scientists revealed that all four of them had regarded the dangers of human contamination by BSE-infected vaccines as, er, anything but remote.

Mr Walker asked Sir Richard Southwood: "In your view, at the time, the degree of hazard from medicinal products was greater than the degree of hazard that applied in the case of oral ingestion?"

Sir Richard replied: "Yes". Later, he told the inquiry: "We really thought the medical problem was severe... We were very conscious, all the way through, of the worry about the vaccination programme. And these were very real deaths. One hundred and seventy deaths had been estimated by the Chief Medical Officer."

If vaccination with BSE-infected vaccines was much more dangerous than eating BSE-infected meat, why did the Southwood committee describe the risk from both with the same reassuring adjective — "remote"? All four scientists were asked this question and all four wriggled with their replies. Sir Anthony Epstein explained: "The seemingly reassuring — I do not accept that it was — use of the word ‘remote’ was done on purpose because the consequences for the vaccination programme, for the use of medicines, would have been really quite disastrous if the public at large had been alarmed by this... it could have had very serious consequences for public health."

So the committee watered down their published warnings about vaccines.

But all four scientists went on to argue with some passion that although their report had appeared to be mild on the subject, they had made every conceivable effort to alert the Department of Health and its relevant agencies to the dangers of BSE in vaccines. All four said they were satisfied that their anxious if private warnings about vaccines would lead to "appropriate action" from the Department of Health.

So what action was taken? The Department issued a statement which emphasised the dangers to the vaccination programme from any public panic about BSE and blandly reiterated the view of the Southwood Committee that the risk of infection from medicinal products was "remote".

Fastening on that magic word "remote", the ministry gave the vaccines the all-clear. There was no need, officials concluded, for pharmaceutical companies to take any steps whatever to insure against the possibility of contaminated vaccines. So the Department of Health and its Committee on Safety of Medicines coolly junked the Southwood committee’s anxious, if unpublished, warnings about the dangers of BSE-infected vaccines.

To this day, no one knows what action was taken to dispose of the five years of stocks of vaccines which had been piled up to initiate the vaccination programme. No one knows whether any of those vaccines compiled before the BSE ban were used on unsuspecting patients, or whether any of the deaths from CJD - a killer disease associated with BSE - can be ascribed to such vaccinations.

Risk of BSE in vaccines revealed

Jonathon Carr-Brown

Political Reporter


Wednesday 8th September 2010Andrew as a baby

Below are details of my Andrews vaccines, when, where he received them and also two batch numbers. Andrew never received the MMR or Whooping Cough vaccine, he also refused to have his school leaving booster injections aged 16.

I have written to the drug manufacturers who made vaccines during the 1980s, 1990s and through to 2000 asking them for details of date made/expiry, processing and the entire ingredients used to make the vaccines that my Andrew received. Vaccines from the same source would have also been given to millions of children/babies across the UK and globally exported.

During the 1980s, 1990s and beyond bovine material from BSE infected herds and human albumen were used to manufacture these millions of childhood vaccines….

Our most vulnerable were put at risk without a thought for their welfare of futures….

During my investigations vaccines I even managed to trace a nurse who administered one of the injections given to my Andrew and she was very very helpful.

Here are the details and record of my Andrews vaccines……

St Mary’s Hospital, St Mary’s Road, Portsmouth. Hants.

2nd September 1983 within a short time of Andrews’s birth he was given a

VITAMIN K INJECTION. This vaccine was given routinely to all babies at birth to prevent problems with their liver. Andrews birth was normal and quick, he was a healthy baby weighing 71bs 10 and three quarter ounces. There were no complications at the birth with Andrew requiring no extra medical procedures or interventions. He was a strong and totally fit baby.

GPs Surgery The Village Practice, 133 London Road, Cowplain, Hants P08 8XL

My Andrew received the following vaccines whilst a patient:

15th December 1983 aged 3months…..DIPHTHERIA, POLIO and TETANUS

9th February 1984 aged 5 months DIPHTHERIA, POLIO AND TETANUS

2ND August 1984 aged 11 months old DIPHTERHIA, POLIO AND TETANUS

KIRKLAND SURGERY. Copnor Road, Copnor, Portsmouth, Hants

Pre school booster aged 4years DIPHTEHRIA, POLIO and TETANUS

(Records for these vaccines have disappeared)

Schools were Andrew would have received his booster injections:

St Judes Infant School, St Nicholas Road, Old Portsmouth, Hants

Copnor Infant and Middle School, Copnor Road, Portsmouth Andrew at school

St Mary’s Hospital, St Mary’s Road, Respiratory Centre, Portsmouth, Hants.

BCG VACCINE BATCH NUMBER E61354A, 29th July 1997

Osborne Road Surgery, Osborne Road, Portsmouth, Hants

Received February 2000

MENIGITIS C VACCINE BATCH NUMBER 43621

Expiry date 06 2001

These are the only vaccines my Andrew ever received; my beloved son never had any operations, stitches or received any blood or blood products. He had perfect teeth and no dentistry apart from a tiny filling a few years before he died.

Before Andrew became ill he was a strong young man, who hardly drunk alcohol, had never smoked and was very careful with his diet. The irony of that statement makes me weep……

So how can a fit and healthy young guy in his early twenties be reduced to shell within months and be dead within weeks?

As Andrews consultant at Southampton General Hospital said

‘A stray burger didn’t do this’……Andrews consultant was very angry that my fit healthy young son was dying through no fault of his own. But the fault of those named and shamed on this website……

What was given to my son during his growing years that was so toxic it made him develop vCJD?

Without question what killed those poor BSE cows …killed my Andrew. the symptoms mirror his decline during the months I nursed him…

But…..how did the toxic poison /rogue prions that killed those cattle get into my Andrews system? What did he ingest?…take in that wrecked his body and destroyed his life and future? What was so specific to Andrew and other victims?

Was is food? Was it vaccines? Was it some other source?

What are the government hiding?

Within certain organisations which the government manipulates are a select number of scientists/officials who hold many of the answers…..

over the years they have gathered significant information which is kept hidden from the public and those families affected by vCJD……

These secrets remain hidden and away from public scrutiny and view.

Those select few who know the truth…if they shared it ….they would find not only their careers but also their freedom and lives ‘at risk’…….

We are still not being told the whole damning truth about vCJD …….

This blog and website is a place where I share and expose the facts, my and Andrews experience and also the stories of other families and victims affected by cjd ..

It’s also a place and forum for the public to hear the truth……

Some of the information I am and have gathered is so sensitive to my investigations that at the moment I am unable to share this with you….as I know this website is monitored by those I am pursuing….. I remain focused and committed…….

A scientist who has worked and helped to develop a test for BSE told me ‘The easiest way to get vCJD is via blood this has been proven, so it stands to reason that some victims of vCJD probably became infected via a rogue batch of vaccines’…..

Polio, BCG and Meningitis vaccines were all withdrawn amid fears of BSE contamination.

Vaccines have a long shelf life and many of these contaminated vaccines were used on unsuspecting children and infants.

Two young men from Eastleigh near Southampton ( 23 miles from our home in Portsmouth) died of vCJD they had received polio vaccines from the same batch at roughly the same location/time.

Tennis Court Road, Cambridge was the place where the human pituitary glands were taken to make growth hormone treatment which resulted in more innocent people dying of cjd. In the same location research was being carried out on TSEs and in the same area research was being conducted with medicines/vaccines…. Was there some sort of contamination? Is that why my Andrew and other victims of vCJD grew inches when they were dying? Andrew grew at least 4 inches when he was gravely ill….one of the first symptoms of vCJD is terrible pains in the legs…….

‘GROWING DURING THE TERMINAL STAGES OF VCJD is impossible’ Professor John Collinge UCL ‘ But from now on we will monitor the height of those suspected or ‘at risk ‘ of developing vcjd’.

Jane Axelrad in her book ‘BSE a Disaster of biblical proportions or A Disaster of British Science ( 1999) has very strong views on vaccines and their implication regarding developing vcjd, she said ‘It is possible that one or two contaminated batches of childhood vaccines have caused vcjd clusters. A more logical and proven method of spreading this type of disease.'

Thousands of potentially contaminated vials of vaccine remained on shelves, to be used until these sources ere exhausted. This action protected the pharmaceutical companies from panic and lost profits, and ensured that the public was not aware of the risk they took when immunizing their children.’


Thursday 2nd September 2010 Andrew

Today would have been my Andrews birthday ….the third one without him...

Every minute of the day I am haunted by his terrible last months and death….every minute of the day I am haunted by the heartbreak that his death and suffering was so avoidable…..

Every minute of the day I wonder what Andrew would be doing now, how he would have looked and most importantly how he would be embracing and living his life….

My son grabbed life and its opportunities with both hands….full of energy, humour and life….its hard to believe that life force, that energy ….. my beautiful boy Andrew will never walk in this life again….will never call out ‘mum’ as he walks through the front door, will never ring me up to tell me about his day ….and he will never feel the sun or rain on his face again….

The tens of thousands of minutes the decades of life that have been unlawfully stolen from him….the sunsets, sunrises, holidays, birthdays, achievements, disappointments, tears, laughter. All those minutes, weeks, months, years have been annihilated from the future he should have had…..........his footprints will never appear in the sand again…..

Today I also think back to that day 2nd September 1983...when my violet eyed Andrew

was placed in my arms for the first time. 71b 10ozs a strong and very healthy baby…..

How Andrew stared so seriously at me and the world around him…how he moved his head and looked around curiously at the world…….

How my heart burst with pride knowing that I would protect my baby son with my life …and all the wonderful hopes and dreams I had for his future……

Those precious moments of brand new life when I held my new born healthy son in my arms.….with the potential for so much…..remain with me today edged with a terrible sadness of how too short my Andrews life was…...

A future wrecked and stolen….a life taken far too soon…...when my Andrew was diagnoised with vCJD….all the lights in my world went out……..

THE DOOR WAS OPEN AND THE HOUSE 
WAS DARK

WHEREFORE I CALLED HIS NAME,
ALTHOUGH I KNEW

THE ANSWER THIS TIME WOULD BE
SILENCE

THAT KEPT ME STANDING LISTENING
WHILE IT GREW

BACKWARDS AND DOWN AND OUT INTO
THE STREET
WHERE AS I’D ENTERED (I REMEMBER
NOW)
The streetlights too were out………

By Seamus Heaney


Monday 30th August 2010Christine, Emma & Andrew

"According to the World Health Organisation, the future public health threat of vCJD in the UK and Europe and potentially the rest of the world is of concern and currently unquantifiable. However, the possibility of a significant and geographically diverse vCJD epidemic occurring over the next few decades cannot be dismissed.

Below are two letters one I sent to GlaxoSmthKline regarding my Andrews vaccines and their reply.

Patrique Offei Medical Information Officer for Glaxo during our first conversation assured me ‘ GlaxoSmithKline have archives going back to the 1980s, it may take about 2 weeks but I will research this and get back to you’

During our second conversation he told me ‘The batch numbers you provided for Andrews BCG and Meningitis C vaccine does not correspond with any of our vaccines’ he continued ‘I tried to find out more information for you and contacted the Department of Health to see if they could help me further and was surprised they don’t seem to have any records before 1992’.

I asked Patrique for his contacts within the Department of Health but he declined.

Patricque advised me go back to my GPs surgery for more information; I had previously obtained Andrews medical records and was advised to contact the vaccine manufacturer direct. Andrews vaccine records were incomplete and his pre school records from the age of four are missing, I have no information about the inoculations he received whilst at school, including boosters. .

Several other parents of vCJD victims have also obtained their sons or daughter medical records and their vaccine records are also incomplete.

I am pursuing this line of investigation as I know that the vaccines that my Andrew received during the 1980s and 1990s were sourced from cattle which were probably BSE infected. I also know for decades that not only has bovine material been used in the processing of vaccines but also human albumen from blood donors.

The drug corporations that continue to manufacture these vaccines have changed their names several times, merged and emerged under different names and companies…and continue to be worth billions globally for their shareholders.

I am not only a journalist but also a mother who needs to know what went into her son’s vaccines …..And whether this could be the source of Andrews’s infection? The CJD Surveillance unit ask every victims family to complete an ‘at risk questionnaire’ and within this document are many questions about vaccines, so these are seen as a ‘risk’ for developing vCJD.

I would have liked GlaxoSmithKline to have provided me with at least the information I had asked about the manufacture process and ingredients of their all vaccines, they have produced during those crucial years when my Andrew was a baby and growing child.

Millions of babies and children wree vaccinated during BSE …and I am sure their families and parents would like to know the truth too….

I will be writing to all the drug companies that manufactured vaccines during my Andrews too short life in an effort to provide information not only for myself but for you the public…….too much connected with vCJD victims have been kept behind closed doors….and I will continue to reveal whilst the establishment continues to conceal…

19th July 2010

Dear Sir Madam,

I would like to know the whole ingredients, processing and source of the below vaccines and whether they were involved in any material sourced from bovine material or from human blood products/albumin. The vaccines below were given to my son.

The vaccines are BCG 29th given on July 1997 Batch number E6135419a.

Meningitis C vaccine given on 21st Feb 2000 batch 43621 expiration date 06

Can you also let me know if any bovine material/ human blood products as well as human albumin were used in the processing and manufacture of vaccines?

Polio 15th December 1983, 9th February 1984 and 2nd August 1984

Diphtheria 15th December 1983 9th February 1984 and August 2nd 1984

I understand both the polio and meningitis vaccines were taken out of circulation because of fears over contamination with vCJD, and that the BCG was also taken out of circulation.

I would appreciate full and comprehensive details on the above.

Details on the above request.

Yours faithfully,

Christine Lord

Letter























































Wednesday 25th August 2010

Every day more people in the UK and globally are receiving confirmation that they Billy and Rose

are ‘AT RISK OF DEVELOPING CJD’, due to medical procedures/medicines, exposure to BSE. .

A letter arrives with the morning post and their whole world has irrevocably changed

These ‘living victims’… have to adjust their family life, work, studies, and lifestyle

to accommodate the fact they now are a public health hazard with an ‘at risk status’. They also have to somehow live a normal life and not be worried that every ‘headache/pain or illness’ is the beginning of CJD.

This takes supreme effort and a high level of strength……and I admire every single individual that I have met and who has contacted me with their story and experiences.

Each and everyone is a heartbreaking story of lives that have been up ended and changed through no fault of their own.

EACH AND EVERY STORY IS DAMNING EVIDENCE AGAINST THOSE RESPONSBILE Dean

.Thousands of individuals across the world are now ‘living victims’ of vCJD’ some have been informed but many more remain totally unaware that they are at risk of VCJD.

Those who have been informed of their ‘at risk’ status have to try and live a normal life, many of them just youngsters in their teens or early twenties. These are the victims that never make the official government statistics, these men and women try to live privately and peacefully in normality…but for them their lives will never be the same…..

I have been informed that recently more UK citizens have been informed that medical procedures they received has now put them at risk of developing the horrific brain wasting disease…… These terrifying scenarios are happening more frequently…as the ticking health time bomb that is vcjd continues to create more ‘living victims’…whose lives and livelihoods will never be the same again……These individuals are not in the media or public eye, because many want privacy and also are concerned about public reaction. They also quire rightly need to try and live as normal a life as possible.

Despite this growing list of innocent victims and thousands of people affected by vCJD…..

Once again David Cameron has refused to meet with myself and others affected to discuss this significant and ongoing public health issue. Cameron and his cabinet continue to politely brush aside my evidence and challenges and in doing so are putting the UK public health at continual risk.

I have been refused a meeting by David Cameron ( 3 times) and also Anne Milton and Andrew Lansley Health Secretary. Their replies never answer my challenges and contain the usual sound bites citing ‘The Phillips Inquiry’ and giving me links to various websites of which I am acutely aware. Edward

VCJD has never gone away and continues to kill and maim on a regular basis. Numbers of cases have not fallen as greater numbers of people become ‘at risk’of developing the disease through medicinal exposure.

Having nursed my only son through the horrors of vcjd, met and interviewed many other victims and their families there is little that a government website which is manipulated to reflect government policy can tell me…..

The Phillips Inquiry ( chair Lord Phillips was promoted twice during his tenure)

Report is now a decade old, was incomplete, witnesses including all civil servants and officials were schooled and rehearsed and important evidence was deliberately withheld. How can that be a true Inquiry? No wonder those responsible for BSE escaped any further investigation when the Inquiry was so hampered by cover up and half truths.

Every Minister and Official from Gummer, Clarke, Hogg, Meldrum, Thatcher involved in the lies and corruption surrounding BSE quote the ‘Phillips Inquiry’ as their

‘GET OUT OF JAIL FREE CARD’…..it would appear that these culpable ministers/officials believe that they are ‘ABOVE THE LAW’……..as they believe the ‘Phillips Inquiry’ exonerates their role in the unlawful killings and maiming of so many innocent people.

Clarke, Gummer and all those named and shamed on this website used the Phillips Inquiry as a tool to conceal their wrongdoings….and ever since have used its report to escape justice and investigation.

I like to remind Clarke, Gummer, Meldurm, Thatcher and their cronies that an Inquiry is not a court and therefore cannot exonerate or dismiss any culpability or wrongdoing……. and that their deliberate actions before, during and since BSE, continued concealment, lies and corruptions remain criminal acts which will be investigated in a court of law in the future…. It’s a fact that deliberate ongoing concealment and destruction of significant evidence remain a criminal act…

Gummer, Clarkes and Meldrums ongoing corruption continues to wreck lives and steal futures….

With blood donations being withdrawn on a regular basis in the USA and globally due to ‘risk of vcjd’ Gummer and Clarke have caused a worldwide scandal and continued health threat for which they must also be accountable……

How much longer can the UK government bury its head in the sand and make out that vcjd is not an ongoing and significant threat to every family in the UK?

How much longer will Cameron continue to support and condone Kenneth Clarke and those culpable?

Why is Cameron being so loyal to the ‘old guard’ Tories such as Clarke….a man who in his sixties is well past his prime?

Where is the government transparency and openness promised by Cameron?

With this blog are photos of three young men in the latter stages of vCJD who died recently………. Billy 21, Edward 25, Dean 25…..where is the justice in this?


Friday 20th August 2010

Below is a list of blood products recalled within the USA because the donor has been found to be at ‘increased risk of vcjd, what this highlights is the length and breadth that one donor’s blood can stretch. Donations from donors in the USA not only stretch far and wide across the States but are also exported to Europe.  This recall which is happening on a frequent basis in the USA highlights the significant threat that vCJD contamination  poses to blood supplies around the world, and the desperate need for a blood screening test for vcjd. All individuals that give blood, tissues and organs must be screened for vCJD.

 

One donor has the potential to infect hundreds maybe thousands of individuals, as blood donation is not just used as whole blood, plasma but also in vaccines and various other medicines. This scenario is terrifying and it also shows how governments across the world are tracking blood donations and recipients. How many recipients who have received potentially contaminated blood world wide have been informed of their status…? The answer is not many!

 

One high level medic at the Prion Unit at Queens Square London, who deals with vcjd patients every day told me ‘There are literally thousand of people walking around worldwide that have no idea they have been put at risk and are at risk of developing vcjd through contaminated blood products/medicines’ UCL University College London, 2009

 

World Expert in prion disease Professor John Collinge added ‘We can no track blood almost to the hour it was donated…and or course recipients.’

 

Thursday, August 12, 2010 USA Blood products, collected from a donor who was at risk for vCJD, were distributed July-August 2010 PRODUCT Source Plasma. Recall # B-1751-10 CODE Units: 4940074276, 4940073715, 4940071471, 4940069659, 4940069033, 4940067949, 4940067284, 4940066697, 4940066186, 4940065501, 4940065059, 4940064400, 4940063689, 4940063201, 4940062301, 4940061045, 4940060118, 4940059432, 4940058612, 4940058035, 4940057327, 4940056944, 4940056102, 4940055531, 4940054916, 4940054377, 4940053585, 4940053352, 4940052476, 4940052053, 4940049911, 4940049641, 4940049033, 4940048708, 4940048167, 4940047623, 4940047193, 4940046601, 4940042440, 4940041959, 4940041499, 4940041081, 4940040644, 4940040281, 4940039741, 4940039321, 4940038905, 4940038496, 4940038086, 4940037701, 4940037068, 4940036329, 4940035745, 4940035507, 4940034949, 4940034585, 4940034066, 4940033784, 4940033321, 4940032928, 4940032509, 4940031829, 4940031581, 4940031046, 4940030789, 4940030315, 4940030001, 4940029514, 4940029296, 4940028529, 4940021502, 4940021131, 4940020946, 4940020482, 4940020217, 4940019234, 4940016753, 4940016190, 4940014889, 4940014693, 4940014270, 4940013994, 4940013711, 4940013405, 4940013024, 4940012532, 4940012060, 4940011866, 4940011351, 4940011205, 4940010801, 4940010451, 4940010120, 4940009762, 4940009437, 4940009264, 4940008972, 4940008801, 4940008451, 4940008262, 4940007933, 4940007763, 4940007371, 4940007289, 4940006944, 4940006904, 4940006543, 4940004253, 4940003913, 4940003525, 4940003400, 4940003161, 4940003016, 4940002791, 4940002646, 4940002380, 4940002307, 4940001986, 4940001797, 4940001533, 4940000538, 4940000373

RECALLING FIRM/MANUFACTURER Recalling Firm: ZLB Plasma Inc., Boca Raton, FL, by fax on April 22, 2008. Manufacturer: ZLB Plasma Inc., Hamilton, OH. Firm initiated recall is complete.

REASON Blood products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.

VOLUME OF PRODUCT IN COMMERCE 122 units DISTRIBUTION IL, NC

PRODUCT Red Blood Cells Leukocytes Reduced. Recall # B-1899-10 CODE Unit: W043210006492 RECALLING FIRM/MANUFACTURER Blood Assurance, Inc., Chattanooga, TN, by telephone on March 31, 2010. Firm initiated recall is complete.

REASON Blood product, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), was distributed.

VOLUME OF PRODUCT IN COMMERCE 1 unit DISTRIBUTION GA

END OF ENFORCEMENT REPORT FOR AUGUST 4, 2010

http://www.fda.gov/Safety/Recalls/EnforcementReports/ucm221345.htm

PRODUCT Source Plasma, For Manufacturing Use Only. Recall # B-2050-10 CODE Units: FD0352541, FD0353287, FD0353501, FD0354000, FD0354230, FD0354726, FD0354938, FD0356975, FD0357302, FD0360235, FD0362117, FD0362267, FD0362670, FD0362917, FD0363328, FD0363526, FD0363892, FD0364098, FD0364535, FD0364753, FD0365175, FD0378255, FD0378534, FD0379225, FD0379524 RECALLING FIRM/MANUFACTURER DCI Biologicals LLC, Farmington, NM, by fax dated August 10, 2009.

Firm initiated recall is complete.

REASON Blood products, collected from a donor who was at risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.

VOLUME OF PRODUCT IN COMMERCE 25 units DISTRIBUTION NC, NY

PRODUCT Fresh Frozen Plasma. Recall # B-1985-10 CODE Unit: W037709092267 RECALLING FIRM/MANUFACTURER Hoxworth Blood Center UC Medical Center, Cincinnati, OH, by telephone on January 26, 2010. Firm initiated recall is complete.

REASON Blood product, collected from a donor who was at risk for variant Creutzfeldt-Jakob Disease (vCJD), was distributed.

VOLUME OF PRODUCT IN COMMERCE 1 unit DISTRIBUTION OH

END OF ENFORCEMENT REPORT FOR AUGUST 11, 2010

http://www.fda.gov/Safety/Recalls/EnforcementReports/ucm222069.htm

Blood product, collected from a donors possibly at increased risk for vCJD only, was distributed USA JULY 2010

PRODUCT 1) Red Blood Cells Leukocytes Reduced. Recall # B-1432-10; 2) Recovered Plasma. Recall # B-1433-10 CODE 1) and 2) Units: X73159; X48910 RECALLING FIRM/MANUFACTURER Blood Assurance Inc., Chattanooga, TN, by fax on September 15, 2009, September 29, 2009 and September 30, 2009. Firm initiated recall is complete.

REASON Blood products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.

VOLUME OF PRODUCT IN COMMERCE 4 units DISTRIBUTION TN, GA, Korea

PRODUCT 1) Red Blood Cells Leukocytes Reduced. Recall # B-1720-10; 2) Recovered Plasma. Recall # B-1721-10 CODE 1) and 2) Unit: GP53048 RECALLING FIRM/MANUFACTURER Blood Bank Of San Bernardino and Riverside Counties, San Bernardino, CA, by letter and email on February 19, 2010. Firm initiated recall is complete.

REASON Blood products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.

VOLUME OF PRODUCT IN COMMERCE 2 units DISTRIBUTION CA, Austria

PRODUCT Recovered Plasma. Recall # B-1769-10 CODE Unit: P87454 RECALLING FIRM/MANUFACTURER Tacoma Pierce County Blood Bank, Tacoma, WA, by electronic notification on April 9, 2010. Firm initiated recall is complete.

REASON Blood product, collected from a donor who was at risk for variant Creutzfeldt-Jakob Disease (vCJD), was distributed.

VOLUME OF PRODUCT IN COMMERCE 1 unit DISTRIBUTION Switzerland

PRODUCT Recovered Plasma. Recall # B-1833-10 CODE Unit: W036509031626 RECALLING FIRM/MANUFACTURER LifeShare Blood Centers, Alexandria, LA, by e-mail on February 18, 2010. Firm initiated recall is complete.

REASON Blood product, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), was distributed.

VOLUME OF PRODUCT IN COMMERCE 1 unit DISTRIBUTION Switzerland

PRODUCT 1) Plasma Frozen. Recall # B-1838-10; 2) Red Blood Cells. Recall # B-1839-10; 3) Fresh Frozen Plasma. Recall # B-1840-10 CODE 1) Units: W038509801565; W038508331750; 2) Units: W038509801565; W038508331750; 4133133; 3) Unit: 4133133 RECALLING FIRM/MANUFACTURER Walter L. Shepeard Community Blood Center, Inc., Augusta, GA, by fax on October 9, 2009. Firm initiated recall is complete.

REASON Blood products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.

VOLUME OF PRODUCT IN COMMERCE 6 units DISTRIBUTION GA, SC

END OF ENFORCEMENT REPORT FOR JULY 28, 2010

http://www.fda.gov/Safety/Recalls/EnforcementReports/ucm220487.htm

PRODUCT 1) Recovered Plasma. Recall # B-1772-10; 2) Red Blood Cells Leukocytes Reduced. Recall # B-1773-10; 3) Fresh Frozen Plasma. Recall # B-1774-10 CODE 1) Unit: 6174086; 2) Units: 6205935, 6174086, 6142542; 3) Units: 6205935, 6142542 RECALLING FIRM/MANUFACTURER South Texas Blood and Tissue Center, San Antonio, TX, by facsimile on September 29, 2009, October 6, 2009, November 3, 2009, and November 4, 2009. Firm initiated recall is complete.

REASON Blood products, collected from a donor who was at risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.

VOLUME OF PRODUCT IN COMMERCE 6 units DISTRIBUTION Austria, TX

PRODUCT 1) Red Blood Cells Leukocytes Reduced. Recall # B-1826-10; 2) Platelets. Recall # B-1827-10; 3) Plasma Frozen. Recall # B-1828-10 CODE 1), 2) and 3) Unit: P51128 RECALLING FIRM/MANUFACTURER Blood Assurance Inc., Chattanooga, TN, by facsimile on January 27, 2010. Firm initiated recall is complete.

REASON Blood products collected from a donor who may have warranted deferral for residency in an area at risk for Creutzfeldt-Jakob Disease (vCJD) were distributed.
 bew
VOLUME OF PRODUCT IN COMMERCE 3 units DISTRIBUTION TN, GA

END OF ENFORCEMENT REPORT FOR JULY 21, 2010

http://www.fda.gov/Safety/Recalls/EnforcementReports/ucm219893.htm

PRODUCT 1) Red Blood Cells Leukocytes Reduced. Recall # B-1683-10; 2) Plasma Frozen. Recall # B-1684-10 CODE 1) and 2) Unit: 9352826 RECALLING FIRM/MANUFACTURER Blood Centers of the Pacific - Irwin Center, San Francisco, CA, by telephone on February 22, 2010. Firm initiated recall is complete.

REASON Unit: Blood products, collected from a donor who was at risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.

VOLUME OF PRODUCT IN COMMERCE 2 units DISTRIBUTION CA

PRODUCT Red Blood Cells Leukocytes Reduced. Recall # B-1736-10 CODE Unit: W038110023096 RECALLING FIRM/MANUFACTURER Florida's Blood Centers, Inc, Orlando, FL, by telephone on January 21, 2010. Firm initiated recall is complete.

REASON Blood product, collected from a donor possibly at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), was distributed.

VOLUME OF PRODUCT IN COMMERCE 1 unit DISTRIBUTION FL

END OF ENFORCEMENT REPORT FOR JULY 14, 2010

http://www.fda.gov/Safety/Recalls/EnforcementReports/ucm219025.htm


Tuesday 17th August 2010Andrew and Mum

Throughout my investigations into the BSE scandal and its lethal human pathogen vCJD, I have come across many clusters of cases of vCJD and sCJD in the same location. This cannot be a coincidence because too many common factors overlap and connect these victims.  These common links point at a specific source of infection to which these victims were exposed. Hot spots across the UK and abroad where toxic BSE material was focused and ingested in a particular area by a group of people. These victims may well have been infected at the same time  and maybe even on the same day. 

Many of these clusters of victims share not only a common location but often the same school, housing, environment,lifestyle or medical care. These finding are significant but every Government agency involved in the investigations of these multiple vCJD deaths has apparently drawn a
blank declaring them mostly a fluke or of  little relevance. The same departments who were involved in the enablement and creation of BSE in the first place, conduct these or oversee these investigations.  Lack of transparency and independence have continued to hamper the truth and all UK government investigations into the BSE scandal and vCJD deaths. All research into vCJD is jealousy guarded by a select few who are manipulated or part of whitehalls agenda. Indpendant and outside scientific help or support is kept to a minimal and everything relevant to public health is kept 'in house'  and secret.  

Nevertheless a lot of information, data and facts about these clusters have been gathered by scientists and researchers funded by the government which remains behind closed doors. Specific information and facts have also been distorted or withheld from the public domain.

Victims Stephen Churchill and John Longley attended the same school together, Sarah Roberts and Matthew Middleton lived just a few doors from each other in the same street and went to the same schools. Richard Roberts, Richard Cole and Marianne Harvey lived in the same area attended  the same schools. My Andrew, Kate Richer and Ben Dale were all at school the same time and fed school meals by the same local authority, they were also part of the schools vaccination programmes. Andrew, Ben and Kate all lived and had connections with Gosport/Southsea. There are just too many common connections between these victims and other clusters, which point at them being infected from a specific source at roughly the same time. In all of the above areas there have also been numerous cases of sCJD,­ many of which I believe have connections with BSE infection. Before BSE cases of sporadic cjd ( naturally occuring form of the disease) was ' one victim in a million'....in the UK in 2010 its now '1 in 33,000' Professor John Collinge December 2009.

In Queniborough at least 5 people died within weeks of each other from vCJD they would have had similar lifestyles and yet the source of their infection was never clearly established. A local butcher who had gone out of business was blamed, even though some of the victims never bought or ate meat from his shop. All victims lived within four miles of each other. Several cases of sCJD were also noted in the area at the same time.

There have been clusters in Glasgow, London, Walton on Thames, Southsea, Eastleigh, Doncaster, Wales, Ireland, Stockport, Kent, Norfolk many have been in less populated locations in which tracebility would have been easier.

Below is an article from the Irish newspaper The Independent, January 11th 2006, reporting on a cluster of vCJD cases in Co Dublin.

Note the comments from the Coroner and the local Garda both of whom tried to investigate further but came up against a brick wall of silence. Note the term used by the Health Service Executive who had been unable to provide information about abattoirs and slaughterhouses because of 'legal reasons'. What about the legal and human rights of the innocent victims who have been killed unlawfully by vcjd­? Note also the involvement of Defra ­whose covert actions quickly shut down any attempt of outside investigation.

Once again the corruption and lies that permate Whitehall and those that created and enabled BSE stretches its tentacles far and wide to keep the lid on the can of worms.. ..to keep hidden the truth behind the deaths of so many innocent people­..the truth and facts that would criminally indict Gummer, Clarke and their cronies.­

Double death uncovers a link to CJD 'cluster'

THE only three Irish victims of the human strain of the deadly CJD disease lived or had family within five miles of each other.

The astonishing revelation of a possible vCJD cluster emerged yesterday at an inquest into the death of 24-year-old Jason Moran from Shankill, Co Dublin.

He died last June from variant CJD (vCJD) - the human form of mad cow disease.

Dublin County Coroner Kieran Geraghty made the link as medical evidence was heard during the inquest.

He called for a State investigation into his discovery.

The court heard Mr Moran, a clerk for Dunnes Stores, had contracted the fatal disease by eating a BSE-infected meat product.

His father, Robert Moran, said his son ate the same meals as the rest of the family, including meat he purchased from one of two local supermarkets - Dunnes at Cornelscourt and Tesco Ballybrack, previously run by Crazyprices.

Witness Dr Michael Farrell, who performed the autopsy on Jason Moran's body, was joint head of the national CJD surveillance unit at Beaumont Hospital.

But he was unware until informed by the coroner that the only other person killed in Ireland by variant CJD in the last ten years - Offaly mother Kay Turner (33) - had close family living a short distance from Mr Moran in Ballybrack.

The coroner also referred to a third person currently fighting the same disease - a young man in his early twenties, understood to be from Bray, Co Wicklow.

"Would you feel that in this situation, when you have identified three cases with geographical links, that probably they should be investigated further?" the coroner asked.

Dr Farrell replied it "would be very reasonable under the circumstances".

He said evidence on Mr Moran's tonsils and spleen indicated he had contracted the disease orally.

He believed the incubation period was up to 15 years, and not fewer than four years in this case.

Garda Rhona Barker, of Blackrock Garda station, said preliminary investigations into the source of local meat had hit a brick wall despite approaching the two local supermarkets.

She added the Health Service Executive had been unable to provide information about local meat supplies or slaughterhouses "for legal reasons". Recording a verdict of accidental death for Mr Moran, the coroner said he believed the links between all three deaths should be explored. "I also intend to write to the Department of Agriculture and Health, to point out the possible connection of the geographical area," he said. "This is a very tragic case, and I would like to extend my sympathies to his family."

Following the inquest, Mr Moran's relatives said they feared Jason had contracted the disease by eating contaminated meat, either imported from Britain or from Irish farms with BSE.

They said they wanted to know how this had happened and who was responsible for the lapse in food safety. "Laws were in place but weren't policed properly," his mother Imelda told the Irish Independent.

"We want someone to be forced to admit they were in the wrong."

His brother Anthony (27) added: "Nothing will bring my brother back. No amount of compensation can stop me from crying every night.


Thursday 12th August 2010Andrew in Central Park

World experts and scientists in the USA studied a range of victims of vCJD  and have been able to  pinpoint a rough table of incubation times for individual victims.

This research and findings are significant, as it would appear that a person who has eaten/ingested BSE infected material has a rough incubation period of 12 years before they become ill.  This is highlighted by the fact that a middle-aged Japanese tourist visited England for just 24 days in 1989 and twelve years later became ill with vCJD.

I have met this mans family who sadly died aged 51 years old. According to scientists

his only exposure to BSE material would have been during his stay in England.

 

What I would challenge is that over a period of 24 days this mans eating habits, lifestyle and exposures during his short stay in the UK could have been tracked very carefully and accurately. So why  hasn¡¯t any data regrarding this mans exposure every been published by the Department of Health? Surely this Japanese victim holds the key to infection and exposure?  What are the government keeping secret about this tourist visit to the UK? Don¡¯t the Uk public have a right to know where this man stayed, went, ate, if he had any medical treatment during his short stay in England? These issues must have been addressed by the Deapartment of Health as Vcjd is a notifiable diseae and a public health issue.

 

 With a incubation period of 12 years it also brings into question how vCJD victim Zoe

Jefferies, who died aged 14,  became infected?.This young girl were the same genotype as the Japanese victim MM.  Zoe  started to show symptoms from the age of 12 years old, so it would seem likely she became infected whilst  a baby  maybe just weeks old. Babies this young do not eat burgers but they drink formula and also have vaccines.

 

Two other victims also add to the facts, Charlene Singh was born in the UK emigrated to the USA when she was 12, Charlene developed symptoms aged 22 . Alison Hutchenson was born in Barbados and emigrated to the UK when she was eight years old she died of Vcjd aged 22 years.  

 

This incubation guide would also mean that the latest young victims including my Andrew may well have been infected from the mid to late 1990s  or  maybe even later.

 These dates would be after the SBO ban when MRM (mechanically recovered meat containing spinal cords/brains) were supposedly excluded from the human food chain. 

 

 BSE still affects UK herds and this lethal material is still in the human food/medicine chain. Not to the extent as in the early 1990s but our food and medicines are not safe or free of  BSE/Vcjd.

 

 So what is the truth?

 Is this why youngsters in their late teens and early twenties continue to die of vCJD in 2010? Is this why the mean age of victims has remained the same for over 16 years when in fact victims should be getting older!

 

This table also highlights the much shorter incubation there is when a person  receives contaminated blood. Roughly 6 and half years from the time a person receives infected blood transfusion to the time they begin to develop symptoms.

 The incubation periods regarding blood are now exceptionally accurate as Professor Collinge told me ¡® We can trace blood donation back to the day even  to the hour it was donated.¡¯ (2009 )

This is why the Department of Health in the UK are aware of ¡®asymtomatic donors¡¯ individuals who remain well but are carriers of ¡®vCJD¡¯ and have the ability to pass vCJD onwards to their blood receipents.

:

 

PRESUMED ROUTE OF EXPOSURE     PERIOD OF EXPOSURE       INCUBATION

 

FOODBORNE

 

Canada                                                 1987-1990                            11-14   years

 

Ireland                                                  1989-1995                             5-10    years

 

Japan                                                   1989                                     12 years

 

United Kingdom (Leicestershire              1980-1992                             10-16years

Queniborough cluster

 

United States                                        1980-1992                             9-21 years

 

BLOODBORNE

 

United Kingdom                                     1996                                     6.5years


Monday 9th August 2010Baby Billy

Check our this link on youtube re vaccines/blood:

http://www.youtube.com/watch?v=UUv-T2x4o9c


People have died of vCJD after receiving contaminated blood. Blood products made from donations including medicines and vaccines also pose a risk.  At least 18 blood donors have died of vCJD here in the UK; some of these victims gave blood for years. Over  half a million people every year in the UK receive a stranger¡¯s blood to help them cope with operations and medical procedures.
 

ALL BLOOD BAGS IN THE UK HAVE THIS DISCLAIMER:

RISK OF ADVERSE REACTION/INFECTION INCLUDING VCJD

An individual who is about to receive blood is usually not in a fit state to read the blood bag or the warning. This warning is not to inform but to legally cover the British government should those patients develop vCJD in the future.  With this blog is a photo of Billy age 2 his mum received a blood donation and could now develop vCJD through that transfusion.

8,000 pints of donated blood is used every day by surgeons in the UK, and yet our blood is not safe or screened for vCJD.

One of the current victims of vCJD a fifty year old hospital worker is dying due to receiving contaminated blood in 2003 after a back operation. Her donor is apparently well. The UK Department of Health  are aware of ¡®asymptomatic donors¡¯ people who have given blood that remain healthy  but are implicated in passing vCJD onwards through their donated blood. A blood donor who gave blood for over 20 years and remains healthy, two of their blood recipients have developed vCJD.

It is estimated that up to ¡®One in a thousand of the UK population could be silently carrying vCJD

2.5 million People in the UK are blood donors.

500,000 people in the UK will receive blood every year during medical procedures.

Anyone who has lived, worked, visited the UK for more than six months since 1980 is not allowed to donate blood abroad. This is causing a lack of blood for essential operations and medical procedures across the globe.  

In one university in Florida USA, at least thirty percent of the students and staff could not give blood because of exposure to BSE and connections with the UK.

The BSE scandal and the significant threat its lethal human pathogen vCJD creates for the worlds blood supply continues to kill in many ways. I was informed from medics involved in last years Australian bush fires that the country suffered an acute shortage of blood needed for burns victims, as many residents due to their UK connections had been exposed to BSE.

Whenever a natural disaster or global accident occurs when l people are in dire need of donated blood, millions of individuals are banned from helping due to their exposure to BSE material.

Yet the UK government whose ministers have created this horrifying scenario continues to block development and validation of blood screening tests that would make the worlds blood supply safe. They withhold blood samples of vCJD victims, information and facts from independent scientists so that understanding of the disease remains within the confines of the British Government and its appointed medics. These scientists are funded, controlled and manipulated by the Government that created BSE/vCJD. The same in-house secrecy and corruption that killed my Andrew continues to weave its web of concealment which continues to hamper research and the truth.  The UK government doesn¡¯t want a test or extensive treatments because they are more concerned about litigation and the can of worms that would be opened. The UK government continues to protect the wrongdoing and lies of those named and shamed on this website and in doing so more lives will be lost unlawfully and needlessly. The UK government is more concerned about keeping a ¡®lid on BSE/Vcjd¡¯ than saving lives and protecting the UK public and global community. meanwhile more innocent lives will be lost and futures stolen¡­¡­¡­


Wednesday 4th August 2010

Below is the medical report of US citizen Linda Andablo who died in February aged 38. I am in contact with Linda¡¯s family and they are convinced that the mum of six died of vCJD. Linda was exposed daily to spinal cords and brains, her job for a decade was to slaughter cattle for the human food chain. Tyson the factory where she worked has already been exposed in a documentary for handling cattle that are ill or diseased.  South Korean journalists during filming for a TV expose found that many of the cattle being slaughtered at Tyson were staggering, ill and suspected of having BSE.

Linda¡¯s family now face financial ruin due to medical bills, but they continue to fight for justice and the truth. I am in constant contact with the family and support them in their

Fight for recognition, Linda never traveled to the UK or was ill before she was struck down by the horrific symptoms that have killed so many innocent people. Linda¡¯s symptoms mirror those of my Andrew and all other victims of vCJD¡­..

 

I admire the bravery of the Andablo family as they become a voice for all victims in the USA ¡­I admire their tenacity and know that their love for Linda will help them to battle on despite facing the powerful beef industry and its many political allies in the USA¡­

Families in the UK and across Europe who have been affected by vCJD continue to support our friends and investigators in the USA ¡­together we form a powerful and truthful alliance¡­¡­

 

Physician Discharge Summary, Parkland Hospital, Dallas Texas

Admit Date: 12/29/2009 Discharge Date: 1/20/2010 Attending Provider: Greenberg, Benjamin Morris; General Neurology Team: General Neurology Team

Linda was a Hispanic female with no past medical history presents with 14 months of increasing/progressive altered mental status, generalized weakness, inability to walk, loss of appetite, inability to speak, tremor and bowel/bladder incontinence. She was, in her usual state of health up until February, 2009, when her husband¡¯s notes that she began forgetting things like names and short term memories. He also noticed mild/vague personality changes such as increased aggression. In March, she was involved in a hit and run MVA, although she was not injured. The police tracked her down and ticketed her. At that time, her son deployed to Iraq with the Army and her husband assumed her mental  changes were due to stress over these two events. Also in March, she began to have weakness in her legs, making it difficult to walk. Over the next few months, her mental and personality changes worsened, getting to a point where she could no longer recognized her children. She was eating less and less. She was losing more weight. In the last 2-3 months, she reached the point where she could not walk without an assist, then 1 month ago, she stopped talking, only making grunting/aggressive sounds when anyone came near her. She also became both bowel and bladder incontinent, having to wear diapers. Her '"tremor'" and body jerks worsened and her hands assumed a sort of permanent grip position, leading her family to put tennis balls in her hands to protect her fingers.

The husband says that they have lived in Nebraska for the past 21 years. They had seen a doctor there during the summer time who prescribed her Seroquel and Lexapro, Thinking these were symptoms of a mood disorder. However, the medications did not help and she continued to deteriorate clinically. Up until about 6 years ago, the pt worked at Tyson foods where she worked on the assembly line, slaughtering cattle and preparing them for packaging. She was exposed to brain and spinal cord matter when she would euthanize the cattle. The husband says that he does not know any fellow workers with a similar illness. He also says that she did not have any preceding illness or travel.

http://www.recordandoalinda.com/index.php?option=com_content&view=article&id=19:cjd-english-info&catid=9:cjd-ingles&Itemid=8

Up until about 6 years ago, the pt worked at Tyson foods where she worked on the assembly line, slaughtering cattle and preparing them for packaging. She was exposed to brain and spinal cord matter when she would euthanize the cattle.

please see full text;

Monday, March 29, 2010

Irma Linda Andablo CJD Victim, she died at 38 years old on February 6, 2010 in Mesquite Texas

http://creutzfeldt-jakob-disease.blogspot.com/2010/03/irma-linda-andablo-cjd-victim-she-died.html

CJD TEXAS 38 YEAR OLD FEMALE WORKED SLAUGHTERING CATTLE EXPOSED TO BRAIN AND SPINAL CORD MATTER

http://cjdtexas.blogspot.com/2010/03/cjd-texas-38-year-old-female-worked.html


Monday 2nd August 2010

Published for the first time (see below) are letters that Sandra G who lost her only son Leon to vCJD has sent demanding the resignation of the new Lord Chancellor, Kenneth Clarke. I am in constant contact with Sandra and she has told me in graphic details the horror of her beloved Leon¡¯s final agonizing days dying of vCJD at just 28 years old.

To date neither Prime Minister David Cameron nor Clarke have bothered to reply or acknowledge Sandra¡¯s heartfelt, factual and emotive correspondence which highlights a significant public health threat.

 

Sandra letters are a voice not just for her beloved Leon, she speaks on behalf of all Mothers across the UK and the global community.  As unfortunately next week, next month, and next year other mums will be watching their son or daughter die a terrifying death due to vCJD...as this UK man made manufactured disease continues to kill innocent people on a regular basis.






























































































Thursday 29th July 2010Andrew at School

Two young men from Eastleigh Southampton died within weeks of each other of vCJD, they had received polio vaccines from the same batch and were inoculated roughly the same time and location. In a statement to a concerned public SEAC member Ray Bradley ( see profile) categorically denied that there was any connection between these young men¡¯s untimely deaths from vCJD and the vaccines. Ray Bradley was head of the CVL Central Veterinary Laboratory (1984) he was one of the government officials who kept the discovery of BSE a ¡®secret¡¯ and evidence ¡®confidential.¡¯ Despite his team of researchers discovering a terrifying and NEW lethal pathogen, which Bradley and Whitehall understood would have devastating effects on animals and humans Bradley and the Government decided to keep this knowledge ¡®low key¡¯ and secret from the UK public.

This allowed BSE infected cattle to continue into the human food and medicine chain. When these life and death decisions were being made my Andrew was just 18 months old. Bradley and Whitehall were aware that bovine material from BSE herds was being used in the manufacture of childhood vaccines, and that human albumin was also used from blood donors to make these inoculations.

Some polio vaccines were eventually withdrawn but not until October 2000 (see press article below) amid fears of BSE contamination. Millions of infants had already been given oral and injectable vaccines which had been sourced from infected BSE cattle, including my Andrew and every young victim who has died of vCJD. (See a list of some of the implicated vaccines, what¡¯s to blame?)

In a recorded interview between myself and Professor Bob Will CJD Surveillance Unit I asked him ¡®Can you categorically assure me that those young lads who died of vCJD who lived near Southampton just 20 miles from our home in Southsea, did not become infected via polio vaccines they received from the same batch.

He replied ¡®No of course I cannot¡¯¡­yet the reassuring statements presented to the media and the UK public from SEAC and Ray Bradley was for parents not to be concerned and there was absolutely no risk or link between vCJD and vaccines.

I also received an email from Bob Will telling me ¡®Under no circumstances are you allowed to discuss, share, publish or reveal our conversations or discussions with a third party without my express permission.¡¯ As I asked medical questions of a world expert in prion disease I will publish these discussions/replies in the knowledge that the public need to know. Professor Bob Will answered those questions with the knowledge and facts he has as a leading scientist in the field of vCJD, whose salary and unit is also funded by the Department of Health and the UK Government.

Too many secrets and lack of transparency surround BSE/vCJD and those cover-ups/half truths and lies killed my son. Why is there such a need to keep relevant and significant facts and information hidden from the public if there is nothing to hide?

My Andrew had polio vaccines in the 1980s/1990s and in 1997 he had his BCG vaccination and in 2000 Meningitis injection. The BCG vaccination programme has been withdrawn, suspected polio vaccines were withdrawn amid fears of vCJD and also there has been fears around vCJD and meningitis inoculations. My Andrew had all his infant vaccines apart from whooping cough and MMR he also refused to have his leaving boosters aged 16. I publish these facts because I wish to be as transparent and open as possible about my Andrew and the risk factors which he was exposed to regarding him developing vCJD.

My Andrew was found to have high levels of mercury in his blood when he became ill with vCJD, Andrew had perfect teeth never had any dentistry/fillings or was knowingly exposed to this deadly chemical. I understand that mercury is used as a stabliser in the production of some vaccines. I have written to the major drug company who produced the vaccines that my son was exposed to; with the very limited information I have of Andrews vaccine record asking for a breakdown of ingredients used, source material and expressing my concerns regarding bse/vcjd contamination. I will publish my letter and their reply in due course.

Many innocent people have died of cjd due to growth hormone treatments which were developed using pituitary glands from cadavers infected with cjd. At the same laboratories where these lethal injectibles were developed, scientists were also researching the deadly BSE. There is also an overlap with some of these researchers working within the development and processing of human vaccines. Did some cross contamination take place within these labs?

Is this why so many victims of vCJD have grown during their terminal days?

I will continue to present the facts via this website/media until the entire truth is revealed about BSE/vCJD and those responsible are made accountable¡­.

UK families need to have an informed choice so that they can make appropriate decisions about their children¡¯s health and wellbeing. I didn¡¯t have that informed choice, as John Gummer, Ray Bradley, Kenneth Clarke and those shamed on this website deliberately manipulated and corrupted the truth about BSE/vCJD and continue to do so by using the establishment and their connections to block my investigations.

The Independent

Polio vaccine withdrawn over BSE contamination fears

By Cherry Norton, Social Affairs Editor

Saturday, 21 October 2000

A polio vaccine that has been given to millions of children and adults was withdrawn by the Government yesterday amid fears it could be contaminated by mad cow disease.

A polio vaccine that has been given to millions of children and adults was withdrawn by the Government yesterday amid fears it could be contaminated by mad cow disease.

The Medical Control Agency ordered GPs to return all unused doses after the finding that it had been produced using fetal calf serum from the UK.

Guidelines in 1989 banned the use of bovine material in medicinal products, but despite repeat assurances from Medeva, the maker, the Department of Health found it was in breach of the guidelines.

The company, which has made one-third of polio vaccines used in Britain since the early 1980s, stopped producing the vaccine last month.

Dr Peter Fellner, chief executive of Celltech, which bought Medeva from Wellcome and owned it from January to October this year, said records relating to the batch of vaccines in question did not "fully clarify" its BSE-free status. "We had assurances from Wellcome that there were no issues over the vaccine and passed on these assurances to the Department of Health. What Wellcome told us was found not to be accurate," he said.

Professor Liam Donaldson, the chief medical officer, said the risk of anyone being infected with vCJD, the human form of BSE, was "incalculably small". The recall comes as it was announced that a report into Britain's BSE crisis will be published next week after a 30-month inquiry.

Medical experts urged parents to continue getting their children immunised, warning that any fall in vaccination levels could result in polio returning to this country for the first time in decades. Worried parents and patients have been advised to see their GPs or contact NHS Direct.

Despite the obvious breach of the guidelines, which were updated in 1999, no action can be taken against any company as the guidance does not become legally binding until next year when it will be covered by an European Union directive.

Andrew Kemp, chief executive of the British Polio Fellowship, which supports victims, said: "What we would hope is that this does not deter anyone from being vaccinated. The vaccine has been extremely successful in combating polio."

Liam Fox, the shadow Health Secretary, said: "The immunisation programme is one of the most important parts of public health policy... It is therefore essential that all information is fully disclosed by the Government to help retain the confidence of an understandably sceptical public."


Monday 26th July 2010Andrew As A Toddler

Several victims of vCJD including my son Andrew grew in height during their final days. Grant Goodwin aged 30 grew 2 inches in 6 weeks, and my Andrew grew over four inches in height. Andrews GP during visits commented ¡®how tall¡¯ he was!? My Andrew throughout his limited life always tried to look taller because he was on the short side. Every expert I have challenged about this has told me ¡®There is no medical explanation for this growth spurt; individuals with Vcjd should not be growing in height.¡¯

I have posed the question to many of the worlds leading experts in prion disease ¡®Why have victims of vCJD who apparently have never been exposed to growth hormone treatment grown during the terminal stages of the disease?

Professor Collinge University College London said, ¡® People with Vcjd shouldn¡¯t grow and I have no idea why this has happened. We are now measuring the height of people suspected or at risk of developing vCJD¡¯.

Many victims of vCJD have also been exceptionally tall 6ft 9inches with siblings and parents much shorter.

Was my Andrew and some of the other victims of Vcjd unknowingly exposed to growth hormones? We know that many people have died of cjd due to growth hormone treatment sourced from cadavers infected with scjd. These growth hormone injectibles were developed in labs that were also involved in other vaccine research and medicinal development could there have been a cross contamination of some sort?

Below is a report from evidence offered by Anne Maddox¡¯s a retired microbiologist about growth hormones used in cattle¡­.

Note her comments about the strangeness of the outbreak and how the pattern of the disease did not fit microbiologist and epidemiologists understanding of the spread and pattern of disease¡­¡­.something as Maddocks said was very strange about BSE its outbreak and resulting epidemic¡­¡­..

The cover up continues ¡­¡­¡­the truth about BSE/vCJD is so sinister that scientists and officials involved in every aspect of BSE and prion research are bound and continue to be bound by the official secrets act. Why? If there is nothing to hide¡­¡­.¡­..

VETS MAY HAVE SPREAD MAD COWS DISEASE - 14th August 1999 by Debora Mackenzie

INEJECTIONS of hormones from cattle brains might have started ¡®made cows disease¡¯ according to a statement made to the official inquiry into the epidemic.

Mad cow disease or BSE is spread when cattle eat infected meat and bone meal, but it¡¯s still not clear why it suddenly appeared at many locations across Britain. Last month, however, Anne Maddocks a retired microbiologist from St Mary¡¯s Hospital London told the BSE Inquiry that experimental treatments using cattle pituitary glands might be to blame.

The pituitary produces hormones controlling growth and ovulation. In the 1980s children treated for dwarfism with human pituitaries developed the human spongiform brain disease, Creutzfeldt - Jakob disease. Maddocks argues that cattle pituitaries may have done the same for British cows. She says pituitary extracts made by vets were widely used in Britain in the late 1970s and early 1980s to boost milk yields and induce multiple ovulation in prize cows. Maddocks believes that ¡®promiscuous¡¯ use of pituitary extracts initially spread the infection, which was then amplified in feed. Roger Eddy incoming head of the Royal College of Veterinary Surgeons, says he has not heard of widespread use of pituitaries at the time. Bit abattoir workers are reportedly preparing to tell the Inquiry that they sold pituitaries to vets for this purpose.

Alterations in the use of bovine pituitary hormones in various countries

This was particularly of significance in countries outside the UK and the bovine growth hormone (BGH) was not licensed for use there. However it is not at all clear that it was not imported and used illegally and as farmers cattle were calued for breeding according to the quantity of milk that they produced (bgh causes milk production) it would be reasonable to consider that it did take place here. Knowing that HGH caused a spread of CJD from rare human cases it is not unreasonable to consider that BGH might do so in cattle. This hypothesis would require the BGH being infected with small amounts of BSE and also that there was another change in the UK that caused the epidemic to take place whereas it did not do so in other countries. BGH use took place after the Second World War and rose markedly during the 1970s. There are now good indications that bovine pituitary hormones were used for both GH and as a method for embryonic transfer and implantation in the UK herd. The way in which BSE seemed to start in the South East of the UK and cases appeared suddenly throughout the UK is odd, and the easy transfer of pituitary hormones around the country could explain this. The sudden rise in the cases of BSE long after the use of MBM started was strange and was the fact that numbers rose so rapidly, whereas if BSE was derived from a single sporadic BSE case we would have expected a different growth pattern of the disease. The subject is fully discussed in the Phillips Inquiry and the explanations are fairly convincing as the method of transfer of the original cases to get the numbers up to a level to cause the epidemic. Farmers have been fairly clear that they did use these hormones but it is unlikely that they will make this public.


Saturday 24th July 2010

Below is a report from Rome regrarding a woman of 42 years of age suffering from vCJD.

I would challenge the numbers of cases that are being officially reported in Europe,

As families continue to battle the authorities across the European Community to get the correct diagnois for their loved ones who they are convinced have died of vCJD. I am in contact with many of these individuals and families affected, Check out the link to the tragic and untimely death of 32 year old GianLuca on Facebook Associazione Gianluca Sgueglia and the Facebook Profile is named Gianluca Sgueglia Onlus.

UK herds continue to be affected by BSE but the Government has raised the age for testing cattle for BSE this has conveniently meant that DEFRA can claim BSE has all but disappeared.
ROME - A 42-year-old Italian woman was reported as the second ever case of madcow disease in humans in the country and is currently hospitalised in desperate conditions, the ANSA news agency said Wednesday.

The woman was diagnosed with a variant of the Creutzfeldt-Jakob disease (CJD) at a Milan neurological hospital in the past months and was then transferred to a hospital in Livorno, in western Tuscany, when she was already in a coma, ANSA said.

It is still unclear how the woman contracted the disease.

In 2009, Italy's health ministry had reported the woman's disease as a "likely variant of the CJD".

The only previous case of madcow disease in humans in Italy was reported in 2002 on the island of Sicily.

On Friday the European Union said it had nearly wiped out madcow disease in animals in Europe.

Only 67 positive cases of madcow disease were identified last year and the animals were old cows that could have been contaminated long ago, the EU said.

In the 1990s, panic erupted after Britain reported a link between madcow and a new form of Creutzfeldt-Jakob disease in humans.

http://www.google.com/hostednews/afp/article/ALeqM5i3cOap1PrjgW2aD_-vZBmUk1snBQ

Una livornese di 42 anni è ricoverata nell'hospice di cure palliative dell'ospedale di Livorno in coma, dopo avere contratto la variante della sindrome di Creutzfeldt-Jakob, il cosiddetto morbo della mucca pazza. La donna è in condizioni disperate ed è ricoverata nel reparto dell'ospedale livornese proprio per effettuare cure che l'aiutino ad affrontare con dignità la fase terminale della malattia. È il secondo caso della malattia registrato in Italia; il primo colpì una donna siciliana nel 2002.

COLDIRETTI: CARNE SICURA «Se confermato, è una eredità del lontano passato facilmente prevedibile, per i lunghi tempi di incubazione della malattia, che non ha nulla a che fare con il consumo della carne italiana, che è del tutto sicuro grazie ad un rigido sistema di controlli introdotto con successo nel 2001 per far fronte all'emergenza Bse». È questo il commento della Coldiretti in riferimento al caso probabile di morbo della "mucca pazza" contratto da una donna di Livorno. «La Bse è praticamente scomparsa da anni dagli allevamenti italiani per l'efficacia delle misure adottate per far fronte all'emergenza come - sottolinea la Coldiretti - il monitoraggio di tutti gli animali macellati sopra i 30 mesi, il divieto dell'uso delle farine animali nell'alimentazione del bestiame e l'eliminazione degli organi a rischio Bse dalla catena alimentare. Ma anche e soprattutto - prosegue la nota - l'introduzione, a partire dal primo gennaio 2002, di un sistema obbligatorio di etichettatura che consente di conoscere l'origine della carne acquistata con riferimento agli Stati di nascita, di ingrasso, di macellazione e di sezionamento, nonch, un codice di identificazione che rappresenta una vera e propria carta d'identit. del bestiame e consente di fare acquisti Made in Italy». Secondo la Coldiretti, «a dimostrare che nei bovini la malattia della mucca pazza è ormai quasi completamente debellata sono i numeri forniti dalla Commissione Ue: nell'unione Europea dai 37.000 animali ammalati del 1992 si è passati, nel 2009, a soli 67, dei quali appena due casi in Italia su oltre 450 mila test effettuati».

GIALLO SULL'ORIGINE DELLA MALATTIA Il caso era stato segnalato come «probabile variante della malattia di Cjd » nell'ottobre del 2009 dal ministero della salute. Secondo quanto riporta oggi il quotidiano Il Tirreno nei mesi scorsi la livornese aveva accusato progressivi disturbi neurologici e ha scelto di farsi curare presso l'Istituto neurologico milanese 'Besta' che le ha diagnosticato la malattia e l'ha sottoposta alle terapie senza riuscire ad arrestare l'avanzata del male. La paziente è dunque stata trasferita già in coma presso il reparto di cure palliative dell'ospedale di Livorno. Non è ancora chiaro invece in che modo la paziente abbia contratto la malattia.

LA SCHEDA DELLA MALATTIA Persone relativamente giovani, che presumibilmente hanno mangiato carne di bovini colpiti dalla malattia della «mucca pazza» e che mostrano disturbi psichiatrici, seguiti a breve distanza dalla comparsa di demenza e disturbi nei movimenti di braccia e gambe: sono queste le caratteristiche che permettono di distinguere le persone colpite dalla forma umana della malattia della mucca pazza e quelle colpite dalla classica malattia di Creutzfeldt-Jakob (Cjd). Quest'ultima colpisce infatti le persone anziane (in media 65 anni) e si manifesta con una demenza che peggiora progressivamente, accompagnata da disordini nei movimenti. La variante umana della malattia della mucca pazza è comparsa 14 anni fa in Gran Bretagna, dove è stata subito associata al consumo di carne di animali colpiti dall'Encefalopatia Spongiforme Bovina (Bse). La forma umana è considerata una variante della malattia di Creutzfeldt-Jakob (Cjd) ed il suo nome è stato ufficializzato come «nuova variante della malattia di Creutzfeldt-Jakob» (vCjd) nel 1997, da un articolo pubblicato sulla rivista The Lancet. A scatenare la malattia nell'uomo è l'alterazione di una proteina naturalmente presente nell'organismo, chiamata prione. Dopo il notevole aumento dei casi della malattia sia nei bovini che nell'uomo, concentrato soprattutto fra il 1996 e i primi anni 2000, da qualche anno si registra un notevole rallentamento nella diffusione della malattia sia negli allevamenti e altrettanto rari sono i casi della forma umana. Proprio nei giorni scorsi il commissario europeo alla Salute, John Dalli, ha dichiarato che l'Europa è uscita vincente dalla lotta contro la malattia, che nel 2009 ha fatto registrare 59 negli allevamenti degli Stati membri. L'ultimo caso di Bse in Italia risale al 2008, in Piemonte e l'unico decesso nell'uomo risale al 2002.

http://www.leggo.it/articolo.php?id=73638&sez=ITALIA

Eurosurveillance, Volume 6, Issue 6, 07 February 2002 Articles S Salmaso1


Tuesday 20th July 2010Emma

Today is my 53rd Birthday, and I will be spending it quietly working on the campaign and having a meal with my daughter Emma and a friend. .

Every family occasion, celebration or special event has a sting in its tail as it highlights my Andrews absence and what he has lost. There is no healing or acceptance when you have lost your only son and brother to vCJD.

I am very proud to announce that my Emma has done exceptionally well in her second year results at University, where she is reading History, Politics and International Relations, despite her grief and heartbreak Emma is like me ¡® When the going gets tough the tough get going.¡¯ My beautiful daughter thank you for bringing light into my darkened world.

Well done Emma your big brother would have been so proud of you!





Saturday 17th July 2010Emma and Andrew

Ten million cattle, sheep and pigs were destroyed in 2001 due to an outbreak of ¡®Foot and mouth disease¡¯.

In 2002 cows and animals remains who had been culled during the epidemic were dug up and reburied amid fears that their diseased carcasses were also carrying BSE which could contaminated the water supply. It was over a year before these burial sites were deemed as dangerous to public health and action taken.

Across England over 160 sites were used for the disposal of these sick creatures including landfills in West Cumbria and Buckinghamshire. Eighty wagon loads of diseased animal remains were moved to another place of disposal from just one farm in Northumberland. Across England thousands and eventually millions of cattle and animals were destroyed on farms and then hastily reburied in neighbouring fields.

A year later the decision to dig up and then rebury millions of animals struck down by foot and mouth came after a risk assessment by the Environment Agency. Surely it was common sense not to bury diseased animals who could also be carrying or incubating BSE on the same land in which restocked animals would graze and be processed into the human food chain?

Cross contamination also took place during the initial disposal of these animals, and the subsequent removal and reburying of their remains, once again the human food chain and our families were not protected from BSE/vCJD.

In a report filed by Peter Hethrington, The Guardian Feb 9th 2002 he wrote:

¡®Richard Dodd s Northumberland County Councillor and farmer who lost 1,450 animals to Foot and Mouth said he was baffled ¡® We hear its not about Foot and Mouth but about BSE¡¯ he said ¡® If it is removed because it poses a risk why was it buried at these sites in the first place? This is happening in places where farms are restocking¡¯

During the foot and mouth outbreak in 2001 over 10 million animals were culled their diseased carcasses initially buried on the farms in which they were raised. until mass slaughter sites were opened to cope with the numbers. These diseased animals many who may have been ill or carrying BSEe were moved around and then buried in sites which had no safeguards for BSE.

Precautions used to eradicate and prevent ¡®foot and mouth¡¯ spreading would have no impact on the rogue prions that cause BSE. The rogue prions that cause this lethal pathogen are virtually indestructible cannot be burnt, buried or killed by sterlisation.

The slaughter, transportation, disposal, burying and reburying of these diseased animals would have increased the likelihood of BSE spreading not only to other livestock but also to humans.

How many animals were destroyed during the foot and mouth outbreaks that were also dying, carrying or incubating BSE? BSE still affects UK herds, during the ¡® foot and mouth¡¯ outbreak it would be impossible to find out just how many of the ¡®ten million cattle and animals¡¯ culled were also infected with BSE.

Is this why so many young people in their teens and early twenties continue to die of vCJD, twenty six years after the first official recorded case of BSE?

BSE continues to remain a threat to human health and life, those young people who have died in the last few years may well have been infected much more recently. This is very much the case according to a high level ex Government Minister who told me ¡®All victims of Vcjd who have been diagnosed since 2007 were infected after 1997¡¯ This high ranking Whitehall official told me many eye opening facts over and extended lunch.

Details of this recorded interview with the ex Cabinet Minister will be published by me in due course.

By the extermination of so many cattle in 2001 it was another way of DEFRA clearing the books ¡­.the cover up spreads like a spiders web through the establishment, but fortunately there are men and women of integrity helping me to gather evidence and to pursue those responsible¡­..


Wednesday 14th July 2010

An Italian family whose lives have been broken by the death of their son and brother GianLuca have set up a foundation in his memory. The Sgueglia family are convinced that 33 year old Gianluca died of vCJD and are currently battling the authorities in Italy for the correct diagnosis. What they have found as a family affected by this horrific disease was a lack of support, consistency, transparency and information and the ¡®Gianluca Sgueglia Foundation has been formed to help families and victims of cjd. Families affected by CJD across Europe and globally feel isolated and their vulnerability is often used by the establishment to intimidate and marginalise.

The Gianluca Sgueglia Foundation is a non profit organisation and though conferences, publications, videos and a website is hoping to give accurate, transparent and factual information about the disease. Its aims are justice, truth, openness and understanding. Below is an open invitation from GianLucas brother and organiser of the foundation Antonio.

To obtain a brochure or further information contact associazionegianlucasgueglia@yahoo.it

GIANLUCA SGUEGLIA Gianluca

ENCEPHALOPATHIES

The reasons that drove me and my parents to form a Foundation in memory of Gianluca are many but more than anything else they are undoubtedly linked to the promise that we made to him before he passed away. Yes, we made a promise to him that we would do anything it would take to restore his right to a correct and true diagnosis.

This is a right that we believe to be an inalienable right for anyone and more so in a case such as Gianluca¡¯s one; a case where a life full of projects and dreams was broken and taken at such a young age from a terrible disease.

We strongly desired that the Association was incorporated and registered on the day of the anniversary of his passing. In fact, exactly one year ago Gianluca was released from the chains of his suffering and and from the terrible illness that struck him. On that very day he finally regained his freedom after years of suffering, sacrifices and limitations.

Death is certainly a great mystery for man and for us all but Gianluca has taught us that in reality it represents, more than anything else, a transformation. Yes, a transformation of the visible that becomes invisible. The intangible that becomes tangible. The material that becomes immaterial. The end that turns into a new beginning.

Thanks to what he taught us with his experience, we, too, wanted to operate a transformation by ensuring that our pain and our anger would be transformed into something different. Yes, a new energy to be manifested in a concrete commitment that, after a year, aims to make sure that

Gianluca¡¯s sacrifice was not in vain but instead can be of help and inspiration to many people.

The non-profit organization named after Gianluca was born on the foundation of all those principles that have animated his life and in that sense it deeply represents and portrays him for who he truly was. Gianluca has endured his illness with dignity and courage that are big enough to be a true inspiration to everyone. And it is with such dignity and with the same courage that today we are committing to this project and to the objectives of the Foundation.

This Foundation is not meant to go against anyone because we do not believe that this would be in any way useful or effective. Instead it is born in favour of justice, truth, solidarity and transparency, principles that were important to Gianluca and that he strenuously defended.

Through his sacrifice, equal to that of a martyr, Gianluca has accomplished and is still accomplishing a very important mission, which is to awaken as many people as possible so that they, too, may recognize the importance of justice, truth, transparency, solidarity and awareness in their lives.

We live in a society in which these principles are too often trampled in the name of profit. A profit often unethical. A profit that protects only the interests of few people while at the same time trampling the right to life and health of many. It was on this ground that sprouted the seed that gave birth to the terrible disease that has affected not only Gianluca and our family, but many other young people around the world and their families. A disease that has been created by the choices of man against nature and that could therefore be avoided.

It is often said that you cannot change the world and that all efforts in this direction can only be in vain. In fact, we, as founding members of the Foundation, strongly believe that the only way to actually do something is to each change our own world. The only concrete thing we can do is begin to bring justice, truth, openness, understanding and solidarity in our own world, in our lives. Only then can we influence and inspire those around us and, who knows, maybe they too will want to do the same and follow our example. Only then the world we live in can actually have a hope of changing and improving. Basically this is the only real contribution that each of us can bring.

The "Gianluca Sgueglia" Foundation has made a choice to bring its own contribution, a contribution of solidarity and inspiration that is born and is based on these values because these were Gianluca¡¯s values. To this end, Gianluca¡¯s experience will be told to as many people as possible in the world through conferences, publications and videos and through a website that will tell his story and provide consistently accurate and transparent information.

The invitation is open to anyone who feels that the values and goals of this Foundation are in harmony with their own. Any help in this respect can only be highly appreciated and welcomed.

We want to take this opportunity to thank Gianluca's friends and relatives who wanted to help us and walk together with us on the path of this new project. Your support is very important to us, you give us great strength and inspire us to move forward.

Finally, thanks to Gianluca for the example of love, dignity, courage, generosity and perseverance that you left to me, your brother, and to our parents, and to all those who were close to you and whom you loved. Your constant guidance and how you illuminate our paths is the greatest legacy that we could never hope to receive.

With love,

Antonio Sgueglia


Friday 9th July 2010

Hunstanton CJD dad dies aged just 25

Dean


Published on Tue Jul 06 08:00:30 BST 2010

DAD-of-two Dean Burrell has lost his brave fight against the crippling disease CJD at the age of just 25.

But through donation of his organs, it is hoped his death will now help others.

Dean, who is father to Chloe, 5, and Charlie, 2, died in Swaffham¡¯s Meadow House Nursing Home on June 24, with his family around him.

Doctors told his wife, Sarah ¨C just two days before his 25th birthday last November ¨C they were 99 per cent sure he had ¡®variant¡¯ CJD or Creutzfeldt-Jakob disease, a debilitating disease which, commonly known as the human form of Mad Cow Disease, affects movement, actions and memory.

Sadly, there is no known cure for CJD and Sarah (23) ¨C whom he married only last July ¨C decided she would like his organs to be used for research to help others.

Doctors in London are to carry out tests on Dean¡¯s organs in a bid to, in turn, help screening programmes, like those used when people donate blood for transfusions.

The couple, of Northgate, Hunstanton, had previously decided they would like their organs donated.

Sarah told the Lynn News: ¡°If this happened to someone I knew, and I had denied the doctors having parts of Dean to help them, I would never forgive myself.¡±

CJD patients are thought to have contracted the disease after eating contaminated meat.

Scientists think there is a link between infected carcasses or offal processed into cattle feed and vCJD though there is no way of knowing where Dean got the disease from.

It was in 1996 when it was discovered that BSE (so-called Mad Cow Disease) had jumped to humans and the decision was made to remove tissue from beef, such as the spinal chord, which may have carried the agent that causes CJD.

It could have been just been one meal Dean had had, Sarah has previously said.

The disease so far is thought to have affected only around 200 people in Britain in the last 30 years ¨C though there are fears many more cases will be uncovered.

Reportedly, up to one in 4,000 people could be carrying vCJD without showing symptoms.

Dean, a scaffolder who used to work at Narford, near Swaffham, first noticed something was wrong as early as last August as he had become stumbly, lacked co-ordination and was very tired.

As his health deteriorated, he was helped by the Norfolk Hospice Tapping House and also Meadow House where he had stayed since March.

Local people previously undertook fundraising to help Dean, who was able to see his beloved Manchester United play, and enjoy a trip to Euro Disney, before his death.

A funeral for Dean will take place at the Union Church in Hunstanton ¨C where he married Sarah on July 18, 2009 ¨C on Thursday, at 2pm, followed by cremation at Mintlyn.

It is requested no black be worn but that men wear sports shirts and the women wear red. Family flowers only are requested though donations for Meadow House and Tapping House can be made.

¡°I want it to be celebration of his life,¡± Sarah said.

Thanking those who had supported her, she included Hunstanton Infant School who had sent books about stars home for the children.

¡°The children say daddy is a star now,¡± Sarah said

Sarah was among those family members, also including Dean¡¯s mother, Marie Dugard, who was with him when he died.

Earlier this year, Mrs Dugard took part in a march in London in a bid to raise the condition¡¯s profile.


Wednesday 7th July 2010

Below is the reply from Nick Clegg, regarding my letter to the Deputy Prime Minister demanding the resignation of Kenneth Clarke . My response to Nick Clegg is below.

My challenges for justice and the truth¡­¡­my questions about culpability for all the innocent victims of vCJD were not answered¡­.

¡®IN A TRUE DEMOCRACY THE STATE HAS NO RIGHT TO REMAIN SILENT¡¯

Heather Brooke (The Silent State)



























Ms Christine Lord

2 Wilton Terrace

Southsea P05 2BQ

Tel 07828230158

mschristinelord@aol.com

www.justiceforandy.com

Dear Nick Clegg,

JUSTICE FOR VICTIM OF VCJD

VCJD SIGNFICANT ONGOING THREAT TO THE UK PUBLIC

I have received a communication from Mrs S Silver, informing me that you received the copy of the letter I sent to Kenneth Clarke demanding his resignation.

I now enclose a copy of another letter I have sent to David Cameron requesting for the second time a meeting with the Prime Minster and/or Andrew Lansley, I would appreciate your comments on both these letters and the opportunity to discuss with yourself the significant ongoing health issues that I have raised.

I am hopeful that as you have ¡®registered the contents¡¯ of my last and the contents of the enclosed correspondence that the factual issues I continue to raise are eventually acted upon and recognised for the truth. A truth that continues to remain hidden and manipulated by the sleight of hand, corruption and intrigues of those Ministers and government officials that is culpable for BSE/vCJD, and the unlawful death of my only son Andrew.

¡®In a true democracy the state has no right to remain silent¡¯ Heather Brooke

Yours sincerely,

Christine Lord

encs


Monday 5th July 2010

Check out the youtube links to tributes to my Andrew and Gianluca, they contain many facts about vCJD and also photos of other victims. It¡¯s a powerful tribute to two young men whose Lives were taken cruelly far too soon.

Tribute to Gianluca:

http://www.youtube.com/watch?v=t6v1BEwhflg

Tribute to Gianluca (Italian version):

http://www.youtube.com/watch?v=N-PLP3-os30

Tribute to Andrew:

http://www.youtube.com/watch?v=uFB5MjYs4No

Tribute to Andrew with Andrew's song:

http://www.youtube.com/watch?v=WQAlayi-yJ4


Wednesday 30th June 2010

Tommy Goodwin who lost his only son Grant to vCJD on 16th January 2009, will be challenging the Deputy First Minister of Scotland at an emotional meeting today.

Tommy speaks not only for the loss of his 30 year old son but for all families affected by vCJD.

PRESS RELEASE

GRIEVING DAD CONFRONTS NICOLA STURGEON AND UK GOVERNMENT OVER HUNDREDS OF UNLAWFUL DEATHS.

WEDNESDAY JUNE 30th 2010, 1 PM. SCOTTISH ASSEMBLY, EDINBURGH MEETING ROOM T4.23

A grieving father will confront Scottish Deputy First Minister Nicola Sturgeon during an emotional and challenging meeting on Wednesday 30th June at 1pm. Tommy Goodwin from Glasgow has invited the press to record the face to face interview to dispel the ¡®culture of secrecy and cover ups ¡® that he believes unlawfully killed his son. Tommy (50) lost his only son Grant to the human form of mad cow¡¯s disease on 16th January 2009. Within months the handsome, healthy 30 year old, became totally disabled due to eating beef products infected with BSE. (vCJD is chemically identical to BSE)

Grants untimely death due to the horrific brain wasting disease has spurred his father to seek answers and justice on behalf of the hundreds of victims that have died, and continue to die. On Thursday 24th June Dean Burrell ( 25) from Norfolk died of vCJD he leaves a toddler son and a daughter aged 4years.

Tommy said ¡®I blame Government Officials for Grants unlawful death, they told us British Beef was safe when they knew it wasn¡¯t! In 2010 its time for justice I am hopeful Nicola Sturgeon and the Scottish Assembly will support families affected by the disease. ¡® he continued ¡® Whatever Whitehall¡¯s propaganda vCJD continues to kill on a regular basis, BSE still affects UK herds.¡¯ he added ¡®Official stats are manipulated, true numbers of people who have died and are dying of vCJD are not being recorded. I know because I have been told that my Grant will never appear on the Governments figures¡¯ He concluded ¡® I will also lodge a official complaint with Nicola Sturgeon human vCJD blood samples are being stored incorrectly. WHO recommendations are being deliberately ignored by the DOH which means vital blood screening tests understanding of the disease, its source and prevalence are being blocked the cover-up continues.¡¯

Tommy plans to challenge the Deputy First Minister on these issues:

1. 26 years after the first official recorded case of BSE, 15 years after the death of Stephen Churchill (19)from vCJD, young people in their teens and twenties are still dying of vCJD. Many of these youngsters were not even born when the first images of BSE cattle appeared on TV screens. Why is this still happening in the 2010?

2. Grant was the first officially recognised person in the world to die of vCJD from a different genotype MV. Professor Hugh Pennington SEAC stated ¡®hundreds more will die¡¯ from a second wave of victims. Yet I have been told by the CJD unit ( DOH funded) Grant will never appear on any official stats, despite a Lancet paper and world experts stating he died of vCJD. One death is one death too many from a totally avoidable disease, but the government are falsely reassuring the public vCJD has gone away. Currently there are families nursing loved ones dying of vCJD across the UK, it hasn¡¯t gone away and could be anyone¡¯s son or daughter next! .

3. I wish to lodge a formal complaint now with you as Secretary of Health deliberate misleading information about my son has been sent to other family members who have been affected by vCJD in a effort to stop them pursuing the truth. I will be writing to the GMC naming those individuals and Government Scientists and asking for a complete investigation.

4. In 2000 the World Health Organisation recommended that all human vCJD blood samples are stored in Citrate to aid research, understanding of the disease, treatment and to develop blood screening tests. Blood from UK human vCJD victims are not being stored adequately, in correct quantities, or in frozen whole blood which makes it useless for research or stored in a powerful chemical call EDTA. This is preventing the development of prion assays ( blood screening tests for vCJD) and understanding of the disease. Why is this happening? To protect John Gummer, Kenneth Clarke and those responsible? I believe it¡¯s to make sure we never find out true prevalence in the population and also the exact source of the infection. I would like you to investigate why these precious samples are being stored in a way that blocks research and hampers outside independent help.

5. I was told my Grants blood was ¡®worth millions to research¡¯ so the family agreed that copious amounts of his blood could be taken by DOH medics. Grants family hoped it would help others and prevent further deaths. When I tried to hand over some of Grants blood to independent scientists not funded or employed by the DOH. I was told only 2ml of his blood was suitable. Over 44ml of Grants blood had been stored incorrectly and is of no use to researchers outside DOH. I would like a full investigation into this! As Health Minister I would like you to discover/ publish exactly how many human blood vCJD samples are held by the DOH and UK groups, organizations. Also how much blood is stored by the DOH/organizations which is being taken regularly from vCJD victims and their family.

6. Andrew Lansley Health Minister states 16th June 2010 ¡®The BSE inquiry continues to inform Government Policy¡¯. Vital evidence was withheld, witnesses rehearsed and instead of being a place to protect and reveal the Inquiry became a forum to hide and conceal. Whenever John Gummer, Kenneth Clarke or those in charge during the BSE scandal are challenged over their decisions they always quote the ¡®BSE inquiry¡¯ as a means to exonerate their wrong doing. Does the Scottish Assembly hold the same views as Andrew Lansley and Whitehall? Does the BSE inquiry and its findings inform Scottish Government policy?


Monday 28th June 2010

Below is the letter I received from Andrew Lansley Health Minister in response to my letters to David Cameron and his ministers. The Prime Minister and Andrew Lansley have refused a meeting with me to discuss justice for victims of vCJD and the significant threat that vCJD continues to pose for families across the UK.

I have written again to David Cameron requesting a meeting for a second time to discuss my concerns particularly blood safety and the prevention of future and further deaths.

It would appear that whilst Number ten Downing Street remains firmly shut to Me Stormont and the Scottish Assembly are more open to families who have been affected by vCJD and are supportive of keeping others safe too!

My response to Andrew Lansley and David Cameron¡¯s refusal is below¡­.















































Dear David Cameron,

JUSTICE FOR VICTIMS OF VCJD 
SIGNIFICANT ONGOING THREAT TO PUBLIC HEALTH  

Enclosed is a letter from Andrew Lansley in which he informs me that neither he or yourself are able to meet with me, to discuss justice for victims of vCJD and the significant threat that vCJD continues to pose to the UK publics health and well-being. Last Thursday 24th June 2010 Dean Burrell was the latest victim to die aged just 25 years old he leaves a toddler son and a daughter aged 4 years old.

I request again a meeting with yourself as Prime Minister asking you to support the campaign for justice and the hundreds of UK citizens who have died and the thousands who have been affected by vCJD, including 128 children who have lost a mum or dad to this horrific brain wasting disease, and to also discuss and investigate why people continue to die of this man made manufactured disease. Twenty six years after the first officially recognised case of BSE , fifteen years after the death of Stephen Churchill (aged 19) young people are still dying of vCJD. Many of these young people were not even born when those first horrific images of BSE staggering cattle were broadcast on TV. Why? If infectious material was removed from the human food and medicine chain over 14 years ago? In January Billy Smith born (1989) died aged 21 of vCJD; this terrible brain wasting has not gone away and will continue to kill for decades. Why are official government¡¯s statistics not accurately recording the true numbers of people who have and are dying of the disease?

I find the measured dismissal from Andrew Lansley and you as public servants whose salaries are provide by UK taxpayers deeply upsetting and lacking in judgment. I had hoped with a new Government that transparency and honesty would be its core values. as well as protecting public health and preventing further avoidable deaths due to vCJD.

Since my son died I have campaigned for the truth and the prevention of further deaths of vCJD by supporting individual blood screening tests for vCJD, blood safety is paramount.. I was been invited to Stormont and welcomed by all political parties and their representatives in Northern Ireland, receiving support from Gerry Adams and Ian Paisley. During my four day visit to Northern Ireland I was given a platform to discuss and explore the significant health issues that vCJD poses in 21st century my findings were received with sensitivity and interest by the Northern Ireland Assembly. I lunched at Stormont as well as engaging in proactive meetings with Nigel Dodds MLA Democratic Unionist Party, Michelle O Neill Health Spokesperson Sinn Fein, and John Mcallister Ulster Unionist Party. My investigations and research were taken on board and my findings continue to inform Northern Irelands Assembly on blood safety and the needs of current and future victims of vCJD. Communication continues with these supportive MPs and I am gladdened by their openness and help.

I was also invited to South Korea and met with MPs at their parliament, including Young-Jin Kim Democratic Party, MP Ki ¨CKap Kang Labour Party and they have petitioned the Secretary General Ban Ki Moon for me to speak to the UN about

BSE/ vCJD and the ongoing threat to the global community. I spent three hours in discussion with members at the South Korean Assembly and found them to be aware and proactive in their dealings with BSE and vCJD. This was televised across Korea and Asia. Since my visit many school meals in South Korea are now being sourced from local organic farms to lessen the risk of infectious material being fed to their most vulnerable. I completed a lecture tour of Universities and public meetings in South Korea talking about my experiences and lessons to be learned from UK Government policy.

My short sharp response from Andrew Lansley on behalf of you the Prime Minister

And UK Government is not appropriate for the hundreds who have died thousands who have been affected by vCJD and the ¡®One in a thousand of the UK population probably carrying vCJD¡¯ Professor John Collinge BBC 1 May 2008.

Family members affected by vCJD in Scotland have been invited to meet with Deputy First Minister Nicola Sturgeon to discuss similar issues I have raised in this letter. I am shocked that you as Prime Minister and Andrew Lansley as Health Minister are refusing to meet me a bereaved mum and campaigner, yet the Northern Ireland and Korean Governments welcomed me with warmth, energy and most importantly acted on the issues that were discussed and raised. I am deeply perplexed that whilst the doors of the Scottish Assembly are open to parents affected by vCJD, Number Ten Downing Street remains firmly shut to an English mum who wants justice, answers and to protect other families from the heartbreak she suffers every day.

I am also shocked that the BSE Inquiry ¡®findings continue to inform Government policy¡¯, Andrew Lansley 16TH June 2010. The Inquiry was held ten years ago, important evidence was withheld, witnesses rehearsed and it was a forum that was used to hide and conceal instead of protect and reveal. Whenever Ministers and Officials responsible for the BSE scandal and my son¡¯s unlawful death are challenged by families or the media, the BSE inquiry is always used as a tool to exonerate and obliterate their wrongdoings.

I await your comments and decision regarding my second request for a meeting with yourself and Andrew Lansley.

Yours sincerely,

Christine Lord

Cc Andrew Lansley


Friday 25th June 2010
Dean during the last few months
Dean on his wedding dayAt 10pm last night Thursday 24th June 2010, Dean Burell from Kings Lynn Norfolk, UK. became the another victim to vCJD. Aged just 25 years old Dean leaves his wife Sarah, (24) and children Charlie 20mths and Chole aged 4 years.

His mum Marie is devastated that her once fit,handsome son, who this time last year was preparing for his wedding has died due to a totally avoidable disease.

My thoughts and sincere condolences are with Deans family and friends.

¡®What will survive of us is Love¡¯ Phillip Larkin.





Wednesday 23rd June 2010

Cases of Sporadic or Classic CJD have tripled worldwide since BSE infected material was given free reign into the human food and medicine chain.

Sporadic CJD a previous spontaneous occurring form of the disease was once rare (one person in a million) and affected the elderly.

Since the BSE scandal the chances of developing sCJD have risen to 1 in 33,000 in the UK. Many cases have been much younger individuals some only in their twenties or thirties dying of this once age related disease. Also clusters or pockets of sCJD cases are appearing which indicates a common source or environmental factor. When my Andrew was dying three cases of sCJD were diagnosed locally one of these individuals lived close to my Andrews¡¯s old school, another near to where his grandparents lived. .

So could these rising cases of sCJD really be vCJD?

¡®VCJD is perceived as the most threatening to public health of all human prion diseases ¡®

Institute Scientific Research France

Many world experts believe the explosion of cases of sCJD and even Alzheimer¡¯s is connected with BSE¡­.we face a GLOBAL epidemic of dementia cases in the next decades and this is not just due to an ageing population. Laura Mauelidis Chief of Surgery Neuropathology Department, Yale University USA, conducted a study in which she discovered that people are being wrongly diagnosed in the USA she said ¡®Autopsies revealed that between 3 and 13 per cent of patients diagnosed with Alzheimer¡¯s were really suffering from cjd.¡¯ This means in the USA alone over 120,000 people could be dying of cjd but are being recorded as dying of Alzheimer¡¯s or other related illness.

World experts are also suggesting that there may be different strains of vCJD affecting individuals depending on their genetic makeup. This would manifest with differing symptoms and onset which could mimic sporadic cjd, resulting in wrong diagnosis.

A paper published by Dr Emmanuel Asante, Institute Neurology, London has shown clear evidence that people who have been infected with BSE can present with symptoms similar to sporadic cjd. Dr Assante research developed a key series of animal models of human prion disease.

Dr Asantes team extended their studies across the three different gene types in the UK.

Thirty seven percent of the population will carry the MM gene, Eleven per cent VV and

Fifty two percent MV. We take one gene from our mothers and another from out father; these genotypes are just a product of our family background and not out of the ordinary. So far the majority of officially recognised cases of vCJD have come from the MM genotype. However on 25th September 2008, Grant Goodwin aged 30 from Glasgow, Scotland was diagnosed with vCJD from the MV genotype. The MV gene is believed to afford individuals certain protection against the disease, incubation periods may be longer and the length and severity of the illness may be slower to progress to the terminal stages. I have met frequently with Grants family and spent the day with Grant before he died in January 2009. Grants symptoms mirrored my Andrews but also seemed to be slower in progression. When I spent time with Grant he told me about his job, could move around and although his memory was failing he was still able to co ordinate his movements though very slowly, his symptoms seemed to be taking longer to develop and I believe it was due to his different genotype. However there remains a question mark for me about how long the MV genotype incubation period could be! There are many scientists who have forged their careers and life¡¯s work around incubation periods for vCJD the common theory is that MMs have the shortest incubation period roughly between 5 years and 13 years and MVs can have an incubation period upwards of 40 years. ( this is based on the Fore Tribe in Papa New Guinea who were cannibals and ate the brains of individuals with sporadic cjd the tribe developed Kuru a similar illness to vCJD)

GrantAndy at talksportGrant died one year one month after my Andrew, yet they were two different genotypes. Grant was also just five years older than my Andrew. This could mean that both Grant and my Andrew were infected from a common source at roughly the same time. Another anomaly is Vicky Rimmer she was initially considered the first ever case of vCJD when she became ill in 1993 aged 15 years old. But her diagnosis was overturned at an inquest held in April 2001. . Why? Vicky¡¯s grandmother was told by experts from the CJD unit that Vicky couldn¡¯t possibly have died of Vcjd because she came from the MV genotype.

Her brain apparently also showed signs of both Scjd and vCJD. Dr Assante research

proved different genotypes would also present differently at post mortem.(see his statements below). Professor John Collinge UCL told BBC1 May 2008 ¡®Individuals from different genotypes suffering from vcjd may well present with symptoms that could be diagnosed as sporadic cjd¡¯.

At Vicky Rimmers inquest the Coroner John Hughes stated that if further evidence came to light in the future he would petition the Home Secretary to re open the case. Professor James Ironside from the CJD unit told the Coroner that Miss Rimmers ¡®case was ¡®unique¡¯ and showed signs of both vcjd and cjd¡¯ I have spent many hours talking to Vicky¡¯s family who nursed her through the 4 years of her terminal illness and her family remain convinced Vicky died of vCJD.

Vicky was the same genotype as Grant Goodwin and if she had lived would have been just a few years older.

How could the government be so sure that nobody from the MV genotype could die of the disease in 1997? Were Grant and Vicky infected at the same time from a common source? Was my Andrew infected at the same time too? What is the real incubation period from ingesting infected BSE material to developing the disease? Could it be months or years?

What are the government keeping from the public and families affected by vCJD?

Is this another part of the cover-up? How many other victims of vCJD have died over the years from the MV genotype and experts have brushed aside families concerns telling them ¡®it¡¯s impossible for your loved one to have died of vcjd because they are a different genotype¡¯.

When Dr Assante team investigated how other genotypes would be affected by BSE infection, they found that the disease presented differently in both symptoms and brain pathology. Dr Asante said ¡®We also showed for the first time that BSE infection of the M genotype (genetic make up) can lead to an alternate phenotype (outward manifestation of the disease) that looks like sporadic CJD in addition to the characteristics of vCJD features.¡¯ Dr Asante also found that the brain pathology was different between the genes.

With the extraordinary rise of sporadic cjd and dementia cases in the UK and worldwide¡­¡­in direct correlation with BSE material in the human food and medicine chain¡­¡­how many of these cases and victims have really died of vCJD?


Friday 18th June 2010

The MPs expenses scandal continues as Ministers who are also named and shamed on this website receive golden handshakes and rewards. Many who have stepped down, retired from office continue to take from the UK tax payer and be rewarded for their wrongdoing and thievery.

Douglas Hogg, whose actions have unlawfully killed so many vCJD victims, will receive a £64,766 golden handshake after stepping down as MP. This is to help him ¡®adjust¡¯ to life in the outside world. Just two of his fiddles were £9,466 a year towards a full time housekeeper and £18,000 a year for ¡®gardening services¡¯, which included cleaning his moat. To think my poor Andrew as a UK taxpayer helped to pay for these abusive expenses claims. Douglas Hogg lives in supreme luxury whilst victims of vCJD and 128 children who have lost a mum or dad to vCJD struggle on the breadline.

Victims of vCJD are left desperate for care, equipment and support and families of those affected continue to struggle against financial ruin and hardship. I know this from personal experience I had to fight for every piece of equipment and care for my Andrew. When you have been given the devastating news that your only son aged 24 years has just 6 months to live because he was exposed to BSE infected material, it¡¯s then appalling I had to fight the very bureaucracy that gave him a terminal illness, for basic care to make his dying days more comfortable.

One mother had to carry her son on her back up and down to his bedroom as she couldn¡¯t afford a stair lift. Other families have been left destitute, another mum a widow ended up living in one room of a friends house¡­she lost not only her 20 year old daughter to vCJD

But her home too! Its impossible to pay a mortgage, bills and spiralling expenses whilst caring for someone with vCJD when you are unable to work.

Andrews_last_few_days_a_edit1Time and again I am hearing from families affected by vCJD who are left to struggle for even the most basic support for their loved one. When you devote yourself to caring for a family member who has vCJD it¡¯s very traumatic and 24/7 so working or earning an income is virtually impossible. Many families have not only lost a loved one to the most horrific disease they have also lost their homes, jobs, businesses and careers. Some family members because of the trauma involved in nursing someone with vCJD have never been able to work again and are under psychiatric care. The carers that helped me to nurse my Andrew have had to receive counselling and supervision, and these were palliative care nurses with decade¡¯s experience. One nurse said to me ¡® I have worked with every imaginable terminal illness from motor neuron disease, MS, cancer and Parkinson¡¯s and I have never seen all the symptoms of those diseases in one person and one person as young as your Andrew¡¯. Adding ¡®I go home and dream about Andrew every night nursing him has affected me for ever.¡¯

This is the legacy those architects and enablers of BSE have left the UK public.

John GummerJohn Gummer, who fiddled his expenses over many years including claiming thousands for keeping his lawns neat at his stately pile in Suffolk, has stepped down from being an MP. His reward a peerage, this is the man who threatened me with ¡®libel¡¯ and told me that I ¡®should be careful what I said about him¡¯¡­John Gummer throughout BSE constantly reassured us that ¡®British Beef was safe to eat¡¯. when it was lethal to humans.

.Rose Smith who lost her son Billy aged 21, January 2010 to vCJD told me ¡®I stopped feeding beef to my young family as I was worried about BSE. But when I saw John Gummer on TV eating a burger and telling us that British beef was safe, I started to feed my Billy beef products again. It¡¯s because of those Ministers and John Gummer that my only son died of vCJD, I trusted them and they lied to me and to everyone.¡¯ She added ¡® my Billy suffered horrendously for months.¡¯

I challenge John Gummer to put his lawyers on to me ¡­as John Gummer not only fiddled his expenses for many years, fraudulently claiming monies from the taxpayer to feather his luxury lifestyle, John Gummer is culpable in the unlawful deaths of hundreds.

Throughout his time as MP and Minister of MAFF John Gummers lies corruption and cover-ups allowed BSE material in the food and medicine chain., when he knew the risks to human health.

This is the truth, these are the facts..¡­.. ¡­..John Gummer and Douglas Hogg are criminals¡­.. And they continue to reap rewards for unlawfully killing hundreds of innocent citizens and putting millions ¡® at risk¡¯.

I await communication from John Gummer and Douglas Hogg¡¯s legal team¡­¡­


Friday 11th June 2010

Since my blog and letters published in which I demand the resignation of Kenneth Clarke, I have received a groundswell of public support, with emails, texts and phone calls all appalled that a man who has unlawfully killed so many is now head of the UK Justice Department. These communications have come not just from across the UK but throughout our global community, they all believe not only should Clarke resign from his role but that he also should be criminally accountable for his actions and role throughout the BSE scandal.

Below is just one of those emails from Theresa in the USA, which articulates the response from the public.

Kenneth Clarke¡¯s deliberate decisions whilst Health Minister not only unlawfully killed my only son has put the UK population at risk and also our entire global community. Millions ate or ingested BSE infected material not only in the UK but food and medicines which we produced during BSE were exported aboard.

Christine, Kenneth Clarke MP

RE: Kenneth Clarke¡¯s appointment as Lord Chancellor UK

An unbelievable appointment. I am truly sorry for the UK public at large. It will take decades to assess the damage that has been done during his reign as Health Secretary and a few more to determine if what we have done thus far has been even remotely effective.

These are increasingly oppressive times for journalists in the free world seeking answers to problems with long incubation periods created by our leaders.

I hope the UK Mothers unite quickly to express disapproval. There is power and untapped potential in this community of caregivers!!

Today's UK mother has to live with the reality that she will most likely be caring for an elderly parent with dementia and the almostHeadstone unbelievable notion that she may be forced to do the same for her child while she herself may be incubating a fatal neurodegenerative disease.

Is Democracy dead? On this side of the Atlantic, on January 21, 2010, 5 Republican appointees to the U.S. Supreme court struck down important laws and regulations limiting corporate influence on election and public policy. The following is a link that can be passed on. It is from the Center of Media and Democracy. http://tinyurl.com/AmericansBeforeCorporations

Again Christine, I am sorry you must endure this. I feel your pain and frustration and wish there was something more than telling you this that could reverse this situation. We all suffer from that appointment...we just don't know it yet.

Theresa USA


Monday 7th June 2010

Below this blog is the very short reply from Kenneth Clarke, from the letter I sent him in May. I refuse his insincere condolences, his words of sympathy are not genuine or true. Kenneth Clarke is a man without integrity or morals. His portrayal of a bloke who likes cigars and a pint is a facade created by the hundred or so people he employs to put a spin on his profile. In reality he is bullish, short tempered, arrogant and ruthless with little emotion or thought for the ordinary man or woman in the street. He is a multi millionaire a lawyer and a calculating machine a man with no conscience or grace. Young Zoë Jefferies who was just 12 years old when she developed vCJD to young Billy Smith who died aged 21 in January of vCJD, these were decent UK citizens our future generation, they in their short lives had compassion and integrity¡­ something Kenneth Clarke has never possessed. This is the man that now heads our justice system¡­..

If he had a decent bone in his body he would have long ago retired from public life and at the very least said sorry and take responsibility for the hundreds of past  and continuing victims of vCJD¡­.victims of his greed, lies and corruption.

Once again that old chestnut the Philips Inquiry is being used by Clarke to exonerate his and other ministers and officials involved in the cover-ups surrounding BSE and vCJD. Witnesses at the Phillips Inquiry were rehearsed and evidence was withheld. The Philips Inquiry was never in the best interests of the public or victims, but has been used ever since as a smoke screen to hide wrongdoing and lies.

Kenneth Clarke calls my truthful facts and exposure of the truth as allegations¡­.well I challenge him to take me and those factual allegations into a court of law¡­I am ready and waiting to hear from his lawyers¡­I would want him to justify why he remains a free man when he is responsible for so many innocent deaths.

Whenever I see footage of those staggering cows in the final stages of BSE, I see all the young people I have visited and talked too as they too died of vCJD¡­..and Kenneth Clarke is responsible for those deaths¡­¡­he holds the smoking gun that killed them¡­.

I am unafraid as I am telling the truth. and Kenneth Clarke and those named on this website are culpable for the unlawful death of my son, hundreds who have died of vCJD, thousands that have been disabled and affected by the disease and tens of thousands who may be silently carrying or incubating the horrific disease. I warn Kenneth Clarke and those named on this website that they are running out of time and places to hide¡­and even as Lord Chancellor, Kenneth Clarke is not above the law¡­¡­and that justice and truth always finds a way¡­¡­.

Below is also a brief reply from the David Cameron¡¯s office telling me that my letter to him asking for transparency, justice and accountability regarding those responsible for vCJD, is receiving attention. I also asked for the resignation of Kenneth Clarke. I await
David Cameron¡¯s and Nick Cleggs reply.

Letter from Kenneth Clarke QC MPLetter from 10 Downing Street


























Wednesday 2nd June 2010

Below is the latest  news from Amorfix the company who developed a blood screening test for vCJD. Their most recent trials using a  blood sample from a vCJD victim failed¡­¡­totally¡­? WHY HAS THIS HAPPEND?

These  negative results have come as a  shock to the medics and scientists involved in these trials, also to campaigners like myself who have followed Amorfix  who were striving to develop and implement mass blood screening tests for vCJD.

This apparent wipe out of Amorfixs scientific/medical research into vCJD blood screening raises many significant questions and challenges. Not least the accessibility and availability of vCJD blood and other samples given to independent scientists outside the remit of the NHS and Department of Health. There is a complete lock down and ownership of vCJD human blood and body samples by the UK Government, which  echoes the travesty surrounding  BSE.
 Throughout the scandal  BSE infected material was owned by the government, this hampered any outside independent scientific support which helped to keep the source and originators of the infection protected and in-house.  This culture of secrecy and cover ups  killed my only  son. The lack of transparency and openness encouraged by the Uk governent which sourrounds all aspects of vCJD  including the Amorfix blood screening tests highlights the question......

 ¡®DOES THE  GOVERNMENT REALLY WANT UK BLOOD DONORS TO BE INDIVIDUALLY SCREENED FOR VCJD?¡¯

Was the Amorfix test viable?  Was its development scuppered by the UK Department of Health to protect the architects of BSE? Can the rogue prions that cause vCJD be detected in  human blood? Are blood screening tests already BEING USED SECRETLY in the UK? Why are the Government and its Whitehall cronies so determined to stop any individual blood screening test for vCJD? 

In October 2009 the Amorfix test ¡®Detected prions in blood from non human primates, that had been infected orally with BSE¡¯ this trial also ¡®Detected prions in a clinical and pre clinical primate¡¯ which means the test could evaluate the disease during its terminal as well as its incubation/carrying phase. Amorfix were considered to be the lead company in the world regarding their vCJD blood screening test with its high levels of ¡®Specifity and hundred per cent sensitivity.¡¯ It had success when it tested 39,000 blood donors in France and the support of the French Government. 

But when it came to testing human blood samples supplied from a secret source by the UKs DOH it has failed¡­and was not able to detect any rogue prions in the blood.supplied ...¡­something is not adding up¡­and something is very amiss¡­¡­..

Before I discuss and answer the above questions, using my experiences, findings and the facts. I must qualify that I have no financial, political or corporate gain supporting any test or medical research in the field of vCJD. I am a mother, campaigner, journalist a educated and aware middle-aged woman. One of the campaigns goals is to prevent future and further deaths of vCJD via the UK and global blood supply. I and other families affected by vCJD have no other agenda¡­..so the facts and experiences that I am going to present to you now are truthful, honest and transparent. I have no one pulling my strings, no threat of loosing my career or funding if I speak the truth¡­..I cannot be bought or silenced¡­.these are the facts..... and the truth ......

Qualities that have been continually compromised and besmirched by the Uk government and its Whitehall cronies who do not under any circumstances want blood donors individually screened for vCJD.

Amorifx is not the first or the last company who have been involved in the development of blood screening tests for vCJD. Here in the UK we face a ¡®Secondary wave¡¯ of victims of vCJD through blood, blood products and medical procedures, as people can ¡®silently carry vCJD¡¯ and pass it on through medical proceedures/iinterventions. It makes sense to be able to use a simple blood test to screen individuals every time they give blood, have a  invasive medical procedure, operation  or donate cells, tissues and other organs. So why  in 2010 isn¡¯t this happening?

Why isn¡¯t a test already in place and routinely used to screen our blood donors?  Politics and the need to keep a lid on evidence and the source of BSE/vCJD have always been paramount before the safety and health of the UK public. Approximately  81 million units of blood every year  is tested for HIV and Hep C. So a screening test for vCJD  is a must when at least 14,000 of the UK population could be silently carrying the disease. We exported BSE to every country in the world so our global blood supply is also at risk. The Uk spends tens of millions of pounds every year trying to keep our blood supply safe ( its not working one of the latest victims of vCJD is dying after receiving a blood transfusion in 2003), a blood screening test would be cost effective and simple to implement.  

I need to explain to you how tests that could be routinely used are being held back deliberately by the UK Government.

Over the last few years Amorfix has been at the forefront of cutting edge scientific research in the development of prion assay tests (screening tests) for vCJD and  diagnostic tools for forms of dementia, such as Alzheimer¡¯s. During the trials for their vCJD test they have screened with the support of the French Government over 39,000 blood donors anonymously in Montpellier France; their test was successfully defined inside and outside the lab. As well as the backing of the French Government the UK Government also put Amorfix under contract¡­.why? If the test was so poor and likely to fail? Once Amorfix signed this contract they were unable to speak openly to the media, they were effectively gagged, so were unable to complain openly about their dealings with the Department of Health. From various reputable sources  and my own experiences I discovered continual blocking, delays  and political intrigues  surrounding the validation of the vCJD test. Increasingly I heard of the frustrations and then fear that the test would never see the light of day from individuals within the Deaprtment of Health  who back Andrews campaign as well as  from scientists and medics involved. 

Again and again the test completed trials set by the UK Governments strict procedures and guidelines, so that the Amorfix test continually enhanced the specifity of their test¡­¡¯99.95 percent exceeding the 99.85 percent recognised by the Blood Transfusion service¡¯ The Canadian Company initially were led to believe it would only be a short time before the test would be validated and implemented within the UK blood transfusion service. 

Why would expectations be raised to such a level by the UK Department of Health if the test was not viable? Why did Amofix press releases show increasingly positive results declaring ¡®Amorfix  has developed the most sensitive and specific test in the world¡¯?

The biggest stumbling block seemed to be accessibility to human vCJD blood samples; Amorfix had proved inside the lab with spiked brain material and with their trial on blood donors in France that the test was successful. What they now needed for total  UK validation was human vCJD samples. 
This is where I and other families who have been affected by vCJD tried unsuccessfully to help¡­¡­

Department of Health and its Whitehall cronies repeatedly stalled and blocked the validation of the test by withholding blood samples from vCJD victims. I tried without success to hand over some of my Andrews blood to Amorfix, as  did other UK families. We as families affected by vCJD were very aware of the scarcity of these samples but after reflection, consideration of many research papers and talking to experts not connected with Amorfix. We all believed that Amorfix test was well on the way to developing an individual blood screening test, that would eventually save many lives. We also knew that helping companies to develop such tests would also eventually lead to treatments and more understanding of the disease. Too many scientists involved in prion research in the UK are being funded by the very organisations/people and government departments that allowed vCJD to flourish in the first place. 

Too many companies involved in the BSE scandal  now hold the purse strings and  fund many of the top research scientists who are responsible for storing  human vCJD. blood, brain and body samples. 

 Familes  knew that if we  were involved in the handing over of our loved ones blood  that they would be bonafide samples and could be double checked for authenticity.  

After months of negotiation between victims families, Department of Health, Whitehall and Amorfix, myslf and  other families were ready to hand over those precious blood samples from our children to the company based in Canada. 
The next step would hopefully be validation and the rolling out of individual screening tests for the UK blood supply. No family member including myself had any financial political or corporate gain from this process. Remember these are the last physical remains of my beloved boy¡­I only considered giving these to Amorfix because I believed a blood screening test would result that could save lives and prevent further deaths.. no way would I have considered this option without talking, discussing and finding out at length everything I could about prion assays and screening tests.

I was about to sign the contract when I was informed by a Scientist that works and is funded by the Department of Health and those other shady companies that my Andrews blood was not stored correctly. My beloved sons blood couldn¡¯t be used by Amorfix or any similar test. At the same time another family like me who had also worked for weeks to retrieve their son¡¯s blood was told a similar story¡­.. families who independently wanted to supply human vCJD blood samples¡­to Amorfix were suddenly told at the last minute that none of our loved ones blood would be suitable only blood  samples supplied by the Department of Health from a secret source would be?

For me this was a devastating blow¡­why was I not informed of this at the beginning of negotiations? Why waste months of talking, arguement with medics and government officials if my Andrews¡¯s blood was not appropriate? I had spent long weeks and months talking and investigating every avenue of this procedure. I admit when I heard this devastating news I cried for  hours¡­..once again it appeared that a door had been slammed in my face. But I have bounced back and remain determined. 

Also I am not a scientist and have no idea how or in what manner my Andrews blood has been stored.? 

 I started to feel very worried about the Amorfix test and the likelihood that it would ever become validated! I also began to smell a rat¡­¡­¡­!. Lots of things were just not adding up.....?

During this time another family whose son was still alive but very ill with vCJD offered to help and agreed for him to give blood to Amorfix . This would mean the provenance and honesty of the sample would be without doubt and not compromised. I was going to be present and even planned to take my camera to film the victim and his family. I wanted to make sure this blood would be bonafide and there would be no more delays. The twenty one year old victims mum said to me ¡® Its too late to help my son but I want to make sure that other mums don¡¯t loose their child to vCJD and I want to help our Canadian friends¡¯. Over a period of days and then weeks I arranged for blood to be taken from this young man. Once again Whitehall¡¯s cronies, stalled, prevaricated and brought every possible piece of bureaucracy into play. When an expert finally went to this young mans home to take blood he was dying, his veins had collapsed and no blood could be taken. These continued attempts to sabotage the Amorfix test, to waylay and disrupt grieving families from trying to protect the Uks blood supply¡­..stinks! It has convinced me that the UK government doesn¡¯t want a blood screening test for individual blood donors¡­as they have over the last months and years done everything possible to prevent this occurring¡­..

I and other family members have no idea where the vCJD blood samples which were eventually given to Amorfix by the UK Government  came from? How were these samples stored? Can the provenance be verified? Why was these samples stored correctly and in sufficient quantities when my Andrews and other victims were not?

The intimidation I and other families experienced during these last months as we have tried to support  a blood screening test has been disgusting. I have personally been bullied by experts  who work for the Department of Health who  tried repeatedly to manipulate me and it has not be in the best interest of the UK publics health. I have been subjected to heated arguements, anger, dismissive comments about my intellect to hours of persuasive  claptrap from the most senior medics employed by the Government asking me not to hand over my Andrews blood samples to Amorfix for testing. 

Why?
 

When Whitehall found out that nothing they could do or say would prevent myself and other families from handing over our loved ones blood samples ¡­we were suddenly told that all the samples had either been compromised, were not in sufficient quantities or stored correctly to be used by Amorfix.

Professor Richard Knight CJD Unit told one family ¡® I believe from as early as  2000 the WHO has recommended that all vCJD  blood samples should be stored in a chemical called citrate so that is helps in the development of prion assays¡¯ (screening tests for vcjd)

Most of the blood samples which are being taken  from UK vCJD victims are being stored in a powerful chemical called EDTA which compromises screening tests¡­..why?  This is not following WHO guidelines and means that screening tests will be invalid. 
I have discovered that when blood samples  taken from UK vCJD victims have been stored in citrate many are not in sufficient amounts or have been stored as whole blood and then frozen, both these procredures can hamper and compromise the future development of screening tests. Why is this happening?

BECAUSE IF OUR BLOOD SUPPLY WAS ROUTINELY SCREENED FOR vCJD THE SECRETS OF BSE/VCJD WOULD BE REVEALED, WE WOULD KNOW THE PREVALANCE OF VCJD IN THE POPULATION AND WE COULD ALSO TRACE BACK TO THE EXACT SOURCE OF THE INFECTION.

This is why filtering of blood is being pushed as the only option to safeguard our blood supply, THIS IS NOT TO PROITECT OUR FAMILIES BUT TO PROTECT THE ARCHITECTS OF BSE AND THE ESTABLISHMENT FIGURES WHO CREATED AND CONDONED THIS HORRIFIC DISEASE.... the cover up continues..... 

Once again political careers and the freedom of those named and shamed on this website are being put before the human health of not only the UK population but our global community.

Kenneth Clarke now sits at the head of our justice department, John Gummer has been made a Lord and now a blood screening test that could have saved lives has been suspended.

A test that had ¡®unprecedented success¡¯¡­totally failed when given secret blood samples from the Department of Health supplied by the same puppet masters who created and enabled BSE in the first place. Those that are culpable would be proved to be culpable by a blood screening test and the Government will do everything in its power to prevent such tests developing or being implemented. 

If there is no test currently available for vCJD why are family members, brothers, sisters, parents who have lost are loved ones to vCJD, encouraged to give blood for research at London hospitals?

I have given at least 6 vials of blood for this research. What use can my blood be if there is no blood test? I have filmed this process for a forthcoming documentary.

Why are haemophilliacs who have been exposed to vCJD through blood products made to give blood for research every couple of months? Some haemophilliacs have been threatened with their medicine being withdrawn if they don¡¯t continue to give blood for this research. They are never told the results of this research which remains unpublished and secret.

Why is blood being taken every few weeks from current victims of vCJD to ¡®TEST FOR THE LEVELS OF ROGUE PRIONS IN THE BLOOD?¡¯, if there is no viable test and rogue prioins cannot be detected?  

I been told by experts and scientists that ¡®Of course there are tests available which the government and department of health are using but these are being kept behind closed doors and the results top secret, they don¡¯t want a mass screening test, it would topple many in the establishment¡¯

A top medic in the UK has told me ¡®We have a diagnostic test that can show a person has vCJD and we are using it.¡¯

Once again the architects the enablers of BSE and its lethal pathogen vCJD have been working their particular poison, manipulating events, officials and government policy, in an effort to protect their rocky freedom and careers¡­once again more innocent people will die¡­..once again the lies and cover-ups that unlawfully killed so many people ¡­..Is weaving its corruption through our cabinet and Government¡­.

Unfortunately in the next weeks, months and years more people will die of vCJD through blood, blood products and medical procedures¡­if blood screening tests for vCJD had been allowed to openly openly flourish and develop¡­.lives could and would have been saved¡­..

Kenneth Clarke, John Gummer and their cronies and also other individuals who I am also pursuing¡­.will have more innocent deaths on their hands¡­¡­..and it will not wash away or be forgotten by myself, other families, fellow campaigners and the UK public¡­¡­

I and my supporters remain undefeated, determined and implacable¡­and  I with my coleagues will continue to expose those responsible ¡­¡­..

AMORFIX

Billy and RoseCorporate update on vCJD test development

TSX: AMF

TORONTO, May 31 /CNW/ - Amorfix Life Sciences (TSX:AMF), a company focused on treatments and diagnostics for misfolded protein diseases, provides an update on the development of a blood test for vCJD, one of its six product development programs.

The company has been successful in developing versions 2 and 3 of the test, which differ in the sample preparation steps, and both are four times more sensitive than the first version which underwent testing with vCJD patient blood in December. The company has also been successful in obtaining a rare blood sample from a person in the clinical phase of vCJD. The new versions of the EP-vCJD tests were used to test this sample and it was scored negative by both versions of the test.

"Although we were able to achieve unprecedented sensitivity with brain prions diluted into blood, we have been unable to detect blood prions with the latest versions of the test," said Dr. Neil Cashman, CSO of Amorfix. "At this stage, we believe our other product development programs are a better use of our resources, although future research may prompt reevaluation of this assessment."

The Amorfix test and those of its competitors were developed using blood samples spiked with brain prions from vCJD patients. Amorfix successfully developed the most sensitive and specific test in the world and was the first to access human samples through the UK National Institute of Biological Standards and Control process. Subsequent significant improvements to the test in the last five months did not yield positive results, and the company has reached an impasse until scientific understanding improves or more vCJD patient blood is available. Accordingly the company will suspend the commercialization of the vCJD project allowing a more focussed effort on the development of novel therapeutics and diagnostics which include:

- Our ProMIS(TM) antibody program targeting disease specific epitopes for both therapeutics and companion diagnostics for cancer and other misfolded protein diseases;

- Growing the revenue from our A(4) amyloid testing service for cell culture, tissue and blood in animal models of Alzheimer's disease (AD);

- Development of a human Alzheimer's test adapting the A(4) test protocol to detect aggregated Abeta, the hallmark of the disease, in

human plasma and cerebro-spinal fluid;

- The advancement of our novel antibodies and vaccines for the treatment of ALS and AD; and

- The contract for the development of a liver cancer early detection assay, which is nearing completion.

About Amorfix

Amorfix Life Sciences Ltd. (TSX:AMF) is a theranostics company developing therapeutic products and diagnostic devices targeting misfolded protein diseases including ALS, cancers, and Alzheimer's Disease (AD). Amorfix utilizes its computational discovery platform, ProMIS(TM), to predict novel Disease Specific Epitopes ("DSE") on the molecular surface of misfolded proteins. Amorfix's lead programs include therapeutics and companion diagnostics for cancers and antibodies and vaccines to DSEs in ALS and AD. Amorfix's proprietary technology enables it to specifically identify very low levels of misfolded proteins in a normal sample. The Company's diagnostic programs include an ultrasensitive method for the detection of aggregated Beta-Amyloid in brain tissue and blood of animal models of AD, months prior to observable amyloid formation, and a blood screening test for liver cancer. For more information about Amorfix, visit www.amorfix.com


   

"One in a thousand of the UK population could be carrying vCJD." (Professor John Collinge,March 2008)

To watch the documentary please use this link

www.bbc.co.uk/mediaselector/check/england/realmedia/insideout/south/insideout?size=16x9&bgc=C0C0C0&nbram=1&bbram=1&nbwm=1&bbwm=1

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