December 26, 2005

Protection for Makers Of Vaccine May Backfire

"Len Lavenda, a spokesman for vaccine maker Sanofi Pasteur of Swiftwater, Pa., said the liability exemption is needed because manufacturers can't secure liability insurance for bird-flu vaccines. Insurers regard such products as uncharted territory, he said."

Insurers are right. It is uncharted territory. If insurance companies, who make their living playing the actuarial tables and obsessively measuring the risks down to the person and the penny won't touch the avian flu vaccine, then why should I allow it to be put into my family?

If an insurance company won't insure a home for you on the side of a hill or in a flood plain, then you should not be building there. If an insurance company won't insure a vaccine, should you be taking it?

"Without insurance, "We'd be asked to put the company's entire economic future on the line to produce the vaccine, and we're not willing to do that," Lavenda said."

"Without recourse for compensation, "We'd be asked to put the family's entire economic future on the line to recieve the vaccine, and we're not willing to do that," Taylor said."

Protection for makers of vaccine may backfire
Monday, December 26, 2005
BY BRUCE TAYLOR SEEMAN
NEWHOUSE NEWS SERVICE

WASHINGTON -- A law shielding bird-flu vaccine manufacturers from consumer lawsuits could cause many Americans to refuse vaccination for fear they would have no recourse if it harmed them, some health experts say.

The legislation, which cleared Congress last week, could significantly undermine efforts to ensure widespread protection against a potential avian-flu pandemic, they warn.

Erin McKeon, associate director of governmental affairs for the American Nurses Association, said liability exemptions were partly to blame when other vaccination programs stumbled.

"Look at how the smallpox vaccination program went in 2003, when the president tried to vaccinate half a million health care workers, but really ended up with less than 40,000 because there was no compensation program," McKeon said.

The liability exemption was attached to the defense spending bill. The legislation contains about $3.8 billion to fund strategies for preparing the nation to fight a bird flu pandemic.

Supporters of the liability exemption insist it is necessary to encourage more companies to make vaccine. Vaccine manufacturing is financially risky, drug makers say, partly because the demand for vaccination is transitory. Also, vaccines generally are administered to healthy people who, if they get sick, might blame the vaccine and sue.

Len Lavenda, a spokesman for vaccine maker Sanofi Pasteur of Swiftwater, Pa., said the liability exemption is needed because manufacturers can't secure liability insurance for bird-flu vaccines. Insurers regard such products as uncharted territory, he said.

Without insurance, "We'd be asked to put the company's entire economic future on the line to produce the vaccine, and we're not willing to do that," Lavenda said.

But the Association of Trial Lawyers of America notes that Sanofi Pasteur has signed $100 million in federal contracts to develop bird-flu vaccine even though the liability shield does not yet exist. The association said federal health agencies have concluded liability concerns have little or no effect on vaccine production.

Blocking consumers' rights to take vaccine makers to court would remove an incentive for companies to make safe drugs, the lawyers group said.

Bruce Taylor Seeman may be reached at bruce.seeman@newhouse.com.

December 25, 2005

Bud Loves His Mommy

Lucky Mommy.

A New Look For The New Year

So I thought I would take the holiday break and play with the blog a bit. When I slapped this thing up I didn't really think it would be a permanent thing and spent no time on the design. Cut to a year an a half later. I will probably fiddle with it and try on a few more blogspot looks, or I might just throw out blogger all together. Don't know what I am going to to really.

Ginger
Drunk on Christmas Chocolate

December 24, 2005

A Little Child Shall Lead Them

I first posted this story more than a year ago, and it continues to be an important one to me. It reminds me of the beautiful power of our little ones and impact of their love. I offer it to you again.

God's blessing on you and your family.

Merry Christmas



Autistic child's gift teaches lesson about God's love; leads to church start
By George Henson


THORNDALE—Some people think the days of miracles are past, but Pastor Larry Griffith says he knows better. He’s seen God use a child’s toy to start a church.

Griffith took a step of faith when he prepared to travel to Brazil with Evangelist Sammy Tippit earlier this summer, leaving behind his pregnant wife.

“One of the hardest things I’ve ever had to do was get on that plane instead of staying with her,” Griffith said.

But he still felt God’s leading to go. He received confirmation as he said his good-byes to his two sons.

His oldest son, Dallas, is 9 years old. He also is autistic. His father says Dallas lives primarily in his own world, and the key components of that world are his little toy Hot Wheels cars.

“He is very possessive of his toy cars, and had his favorite one that he always kept with him—his security blanket—in his hand,” Griffith recalled.

While some autistic children are not very vocal, Dallas is. Dallas asked his father to bring him back a car from his trip.

“Part of the price you pay for being a preacher’s kid is that everything is a life lesson,” Griffith said. “So I preceded to tell him that I would try, but I wasn’t sure if I would be able to or not. And he should remember that in Brazil, the children were very poor, and many of them had never had even one car or any other toy.”

Dallas stood before his father for a few seconds and then held out the hand that held his most precious possession.

“He told me to give it to a boy in Brazil. My wife and I were dumbfounded and just stood there in tears.” Autistic children tend to be self-centered and reluctant to share, Griffith explained.

“We knew at that moment that God was up to something very special,” he said.

The flight from Texas to Sao Paulo, Brazil, was a long one, and all the way there, Griffith’s thoughts were drawn back to his son’s gift of his most prized possession.

“I began to see that as a picture of what God has done for us—the way he gave his son that we might have eternal life,” he said.

In Brazil, he preached at First Baptist Church in Jardra, and he recounted the story of his son’s gift. In the midst of telling that story and relating to the congregation how it was a picture of God’s love, he asked if a 9-year-old boy were present. A boy named Jefferson came to front. Griffith presented Jefferson with the first toy he ever possessed on behalf of his son, Dallas, who was giving the first gift he ever gave.

“The congregation just wept,” Griffith said.

After the service, four men said they had been impressed that they needed to share the story of God’s gift of love with people in a nearby neighborhood that had no church. One of the men owned a garage where he worked on cars and said it could serve as a church for the community.

The next day, Griffith and the four men went door-to-door through an impoverished neighborhood. The residents’ poverty had hardened their hearts toward God, he said.

“They said, ‘God doesn’t love me.’ But as we shared the story of Dallas’ gift and God’s gift of his Son, we would see hearts melt, and 27 people gave their hearts to Christ that first day,” Griffith recalled.

The men decided that with so many making professions of faith in Christ, the meetings in the garage could not wait until the next Sunday but needed to start that night. Each of the 27 who had made commitments to Christ was present.

Griffith and the men continued witnessing to the people and telling the story of a boy’s gift and how it mirrored God’s gift. By the end of the week, 131 people had made professions of faith in Christ.

When Sunday came, the garage overflowed with people.

“It was the most amazing thing I’ve ever seen God do—start a church with an 88-cent car,” Griffith said.

The church in the garage still doesn’t have a name. Charter members have to go through paperwork and receive city approval before they have an official name. But unofficially, Griffith has his own name for the congregation.

“I call it First Baptist Church of Dallas.”

Evangelicals Converted on the Environment

Amen.


Evangelicals converted on the environment
By Clive Cookson
Published: December 23 2005

"The Earth is the Lord's, and the fulness thereof" - Psalm 24

Early next year environmental scientists, who have been campaigning fruitlessly to persuade the administration of US President George W. Bush to take global warming more seriously, hope to gain a very influential source of support.

The National Association of Evangelicals, the largest organisation of "born-again" Christians in the US, is circulating among its leadership a draft policy statement that would demand strong action against the causes of climate change.

NAE members - 45,000 churches with a combined congregation of 30m - are sometimes seen as rightwingers who despise environmental issues in general and climate change in particular. But it would in fact be a logical step in the "greening" of churches around the world.

In 1967 the historian Lynn White wrote a critique of Christianity, The Historical Roots of Our Ecological Crisis, which blamed environmental problems on the Christian notion that God gave the earth to people for their use and directed us to exercise dominion over it and all its life forms. Since then, environmentalist church groups have sprung up to promote the opposite view: that God made humanity responsible for looking after the earth.

Until recently, most have been on the liberal wing of Christianity but they are being joined by fundamentalists who can find many biblical references to support "creation care", the favoured term for environmental stewardship.

Sir John Houghton, former head of the UK Meteorological Office and a scientific leader of the Intergovernmental Panel on Climate Change, has been influential in campaigning for a change of heart among US evangelicals on global warming. As a devout Christian, he persuaded some evangelical leaders to come to England in 2002 for a meeting in Oxford at which they were convinced by the scientific case for tackling climate change - and he has worked closely with them ever since.

Mary Evelyn Tucker, co-ordinator of the Harvard Forum on Religion and Ecology, calls the Oxford conference "a hugely important conversion moment for the evangelicals. After that they were going to come on board."

Then, in 2004, evangelical leaders including senior representatives from the NAE and the equally influential Southern Baptist Convention gathered in Sandy Cove, Maryland, for a three-day session of prayer and discussion. Sir John was present there too. From this meeting emerged the "Sandy Cove Covenant", a document spelling out the principles of creation care. "We invite our brothers and sisters in Christ to engage with us the most pressing environmental questions of our day, such as health threats to families and the unborn, the negative effects of environmental degradation on the poor, God's endangered creatures, and the important current debate about human-induced climate change," it says. "We covenant together to engage the evangelical community in a discussion about the question of climate change with the goal of reaching a consensus statement on the subject in twelve months."

With the consensus statement now in the final - and most delicate - stages of formulation, the NAE is refusing to discuss its contents. "I am sure it will be a really positive and influential statement - and will counter the misinformation campaign propagated by the oil industry since 1992," says Sir John.

Evangelicals not bothered about the environment are an "extreme minority who have taken the view that the future of the earth doesn't matter because the whole thing will soon be wound up", he adds. These people believe that the End of Days and the Rapture are at hand. In the Rapture, due within 40 years, "the saved ascend to eternal grace and the rest of us writhe in damnation", as Lord May put it in an address to the Royal Society in London last month. "If you believe this you clearly do not worry about 2050."

The Age of Autism: Gold Salts Pass A Test

The Age of Autism: Gold salts pass a test
By Dan Olmsted
Dec 23, 2005, 19:16 GMT

In a Striking Follow-up to Our Reporting on the First Child Diagnosed with Autism -- and His Improvement After Treatment with Gold Salts -- a Chemistry Professor Says Lab Tests Show the Compound Can 'reverse the Binding' of Mercury to Molecules.

'This does lend support to the possible removal of mercury from biological proteins in individuals treated with gold salts,' Boyd Haley, professor and former chemistry department chair at the University of Kentucky, said Thursday.

The potential significance: Donald T. -- Case 1 among children diagnosed with autism in the 1930s -- showed marked improvement in his autistic symptoms after being treated with gold salts for an attack of juvenile rheumatoid arthritis. That`s according to his brother, who we interviewed earlier this year in the small Mississippi town where he and Donald, now 72, still live.

One theory of autism -- strongly dismissed by federal health authorities and mainstream medical groups -- is that the disorder is primarily caused by a mercury preservative called thimerosal that was used in vaccines beginning in the 1930s. Some parents and researchers who believe autism is, in essence, mercury poisoning are using treatments designed to remove mercury from the body or offset its neurological effects.

Haley is among a minority of scientists who holds this view, and after reading about Donald`s improvement he set out to test whether gold salts have any effect on mercury. 'You follow your nose in research, and when I saw that I thought, yes, this is a possibility,' said Haley.

Haley`s experiment was quite simple: He began with a colored thiol-containing compound. Thiols are the class of molecules that contain a sulfhydryl group (a sulfur and hydrogen atom bound together) and, because of the affinity of mercury for sulfur, these molecules bind tightly to mercury. Thiols are found in most enzymes, and when mercury binds to them, these enzymes lose their biological activity, which is needed to maintain healthy cells, he said.

Haley performed two tests involving inorganic mercury -- the type of mercury thimerosal breaks down to in the brain, he said.

Haley`s compound was designed to turn colorless when mercury binds to it. In the first test, he added the mercury, and the 'optical density' measurement went from 0.23 units down to 0.11 units immediately, and down to 0.03 units in half an hour -- a clear sign that the mercury had bound to the thiol.

In the second test he premixed the mercury with gold salts for two minutes, then added it to the same solution. This time the optical density dropped to 0.11 but then slowly increased back up to 0.23 within about 30 minutes -- 'totally the opposite of the situation with mercury alone,' Haley said. 'The only way this could happen would be for the gold salts to remove mercury from the thiol-containing compound.'

The advocacy group SafeMinds -- which opposes the use of mercury in medicines and provided Haley with the $142 prescription of gold salts to test -- called the results potentially significant but cautioned against premature use of the compound to treat autistic people.

'Clinicians have shown that some autistic children show strong recovery from their symptoms after biomedical treatment,' said SafeMinds` Mark Blaxill. 'So any time we discover a treatment that works in a child, we need to take it seriously.

'According to his brother`s unprompted report, Donald T. recovered from autism after treatment with gold salts. We should be all over that, especially after Boyd`s work. But we need to proceed with care to make sure that this is a safe treatment.'

Haley made the same point. 'Please note that I am not recommending using gold salts to treat autistics, but it would certainly be worth a project if carefully monitored by a physician in a good clinic.'

In August Donald`s brother described to us his 'miraculous response' to gold-salts treatment for a life-threatening attack of juvenile arthritis. Donald was given injections of the salts over a two- to three-month period at the Campbell Clinic in Memphis at age 12 in 1947.

The arthritis cleared up, and so did the 'extreme nervousness' and excitability that had afflicted him, his brother said. Donald also became 'more social.' He went on to college, where he was invited to join a fraternity; worked as a bank teller; and now, in retirement, pursues his love of golf and travels the world. Most of those early patients -- and thousands since -- were institutionalized when they got older or lived in extremely sheltered circumstances, according to follow-up reports. (Donald did not respond to our request for an interview, and we are not identifying him at this time beyond information in the original case study and follow-up.)

Before Haley tested the gold salts, he told us why he thought it was worth investigating.

'Nothing has a higher affinity for mercury than elemental gold. They form bonds that are very tight,' Haley said. Devices designed to detect and filter out mercury routinely use gold, he noted -- and they obviously would employ a less expensive element if gold weren`t so effective. Mercury was also used to extract gold from ore in mining operations.

In the body, Haley said, gold likely is 'attracted to the same places as mercury. They would probably make it to the same spot in the body. It (gold) would probably cross the blood-brain barrier like mercury. There are reasons to think that if you put it in, it would chase mercury down because they`re very similar in their chemistry.

'So you might be able to displace it with the gold. The chemistry gets complicated here, but gold does not do as much oxidative stress as does mercury. The gold isn`t nearly as toxic as the mercury. ... It could take it off the enzyme it`s inhibiting and reactivate that enzyme.'

Haley said he was intrigued that the treatment may have benefited Donald when he was 12 -- old for such a positive response, according to proponents of biomedical therapies. The most controversial such treatment is chelation, which uses drugs in an attempt to pull toxic metals -- mercury in particular -- from the body.

'It doesn`t seem to work with the older kids,' Haley said. 'These older kids are just lost.' But, Haley emphasized: 'Don`t jump on this. Be careful. You can hurt kids.'

That concern was underscored when a 5-year-old autistic child died this year while undergoing chelation in Pennsylvania. Federal officials say it is not a responsible practice, although one advocacy group says more than 10,000 families have tried it, with significant benefit.

December 23, 2005

Veterans Groups Protest Vaccine Liability Protection

The proposal effectively would prevent manufacturers from being sued for the vaccines' effects.
BY BOB EVANS
December 22, 2005
WASHINGTON, D.C.: VACCINE PROPOSAL -- Three groups representing veterans and their families are protesting a plan that protects vaccine manufacturers from lawsuits brought by civilians and members of the armed forces.

In an open letter to President Bush and Congress, the groups said, "subjecting service members to dangerous vaccines while giving protection to vaccine manufacturers is not only a threat to the health of our troops, it is a threat to the ability of our armed services to recruit and keep soldiers."

The groups noted that the legislation strips veterans and civilians of their ability to sue for damages if the vaccines, now experimental, are used and cause someone harm. Under the terms of the bill, the government would compensate victims but the specifics of how that would work and the amount of money was not determined.

The proposal, tucked into a defense spending bill, passed the House early Monday and is expected to come to the Senate for a vote today or later this week.

The veterans groups' letter, and an advertisement they placed in the Congress Daily newspaper on Friday, cites statistics from a story in the Daily Press detailing how the Department of Defense withheld data on more than 20,000 hospitalizations of troops who received the controversial anthrax vaccine from 1998-2000.

The executive director of one of the veterans groups, Steve Robinson of the National Gulf War Resource Center, said the newspaper's discovery of the unreported hospitalizations was a significant event in veterans' efforts to discover the truth about the harmfulness of the vaccine.

Language preventing civilians and others from suing vaccine makers responsible for drugs to fight avian flu or biological weapons was slipped into the defense bill sometime between 11 p.m. Sunday and 1 a.m. Monday by Senate Majority Leader Bill Frist, R-Tenn.

Under the provision, any lawsuit against these companies would have to include proof of "willful misconduct" when it was filed, a standard many legal experts said would be nearly impossible to meet. That means drug makers could be guilty of "reckless" or "negligent" actions and be exempt from punishment by a lawsuit.

The bill would also prevent those who were injured from getting information about the vaccine and its manufacture. Opponents say that would allow manufacturers and the government to hide information on illnesses and other problems caused by a bad vaccine.

The Senate was expected to vote on the measure late Wednesday or today. Democrats and some Republicans have vowed to oppose the measure.

The legislation funds military expenses past Dec. 31, but also creates the lawsuit ban and opens the Arctic National Wildlife Refuge in Alaska to oil drilling.

Frist says the legislation is necessary so that major vaccine manufacturers will participate in the development of new drugs and have confidence that there are sufficient financial rewards.

Robinson and others point out that members of the armed forces are typically the first to receive these drugs in large numbers and the most likely to be exposed to any dangers.

"The drug industry is holding the federal government hostage" by insisting on being immune from lawsuits that might enable veterans and others to get compensation for any harm these drugs cause, he says.

The Age of Autism: Missing in Mississippi - Part 2 or 3

The Age of Autism: Missing in Mississippi
By DAN OLMSTED
UPI Senior Editor

In this -- the second of three parts recounting our reporting on autism since the start of the year -- we revisit the first child ever diagnosed with the disorder.

On a sweltering late August morning we climbed the stairs to a second-floor law office in a small town in Mississippi. We introduced ourselves to the brother of Donald T., the first person ever diagnosed with autism.

Donald was born in 1933; he came to the attention of the medical world in 1938, when his parents took him to see the renowned child psychiatrist Leo Kanner at Johns Hopkins University in Baltimore. Over the next four years Kanner saw 10 more children exhibiting the same unique behavior syndrome, and in 1943 he introduced the disorder in an article titled, "Autistic Disturbances of Affective Contact."

While Kanner did not identify Donald by his full name, we were able to determine his identity and learned he was still alive at age 71. That's what brought us to his brother's office -- looking for clues to the roots and rise of a devastating disorder that seemed rare when Donald was born, but now affects 1 in every 166 U.S. children.

Donald, his brother told us, was out of town. But speaking in a courtly, deliberate manner and without any prompting on our part, he told a remarkable story: At age 12 Donald had been living with a nearby farm couple. "One February day, I think it was, they came to (town) with Don. He had a bad fever and was obviously sick." His joints were swollen and stiff, his brother said.

"My father and mother took him to all various places for examination -- they went to Mayo Clinic, brought him back. He lost his appetite and was terribly emaciated. But anyway, my father was talking to a doctor (in a nearby town) he happened to run into and said, 'It looks like Don is getting ready to die.'"

The doctor said, "What you're describing sounds like a rare case of juvenile arthritis." Diagnosis in hand, his parents took Donald to the eminent Campbell Clinic in Memphis, where he was treated with the then-standard remedy, gold salts. "He just had a miraculous response to the medicine," Donald's brother said. "The pain in his joints went away."

And here's the kicker: "When he was finally released the nervous condition he was formerly afflicted with was gone. The proclivity toward excitability and extreme nervousness had all but cleared up." He also became "more social."

In other words, Donald got a lot better. He went on to college, joined a fraternity, worked at a bank, owns a house, drives a car, belongs to the Kiwanis and the Presbyterian Church and plays a good game of golf despite one fused knuckle left over from the arthritis attack.

And now, in retirement, he travels the world. That explained why he wasn't in town -- he was off having a good time. Last stop: Italy. Favorite city: Istanbul. Because Donald did not respond to a request for an interview made through his brother, we are not identifying him at this time.

Most of the rest of the first 11 children identified by Leo Kanner depended for the rest of their lives on the kindnesses of strangers: They lived in back wards or, if they were lucky, group homes or other sheltered arrangements.

Donald's brother told us Johns Hopkins researchers have been in touch every decade to check on Donald, but we're not aware of any published accounts of Donald's improvement following the gold-salts treatment -- something his brother volunteered to us in a half hour of conversation.

Regardless, the fate of the first child ever diagnosed with the disorder seems more relevant today than ever before. One reason: Some parents, under the guidance of several hundred doctors who have broken away from the medical mainstream, are trying a variety of medical interventions to treat their autistic children.

These range from restrictive diets to cod-liver oil to methyl B-12 shots to the most controversial technique, called chelation (key-LAY-shun). This involves giving a child a drug -- orally, via creams or in some cases, intravenously -- that is designed to pull heavy metals, in particular mercury, from the body. The process carries risks: Earlier this year a 5-year-old autistic child died while undergoing intravenous chelation in Pennsylvania.

The theory behind it -- rejected by federal health authorities and most scientists -- is that in most cases autism is actually a form of mercury poisoning. The mercury in question came from some childhood immunizations, which beginning around 1930 contained an ethyl-mercury preservative called thimerosal. The Centers for Disease Control and Prevention, the American Academy of Pediatrics and other experts say that concern is unfounded, but they recommended in 1999 that it be phased out of childhood vaccines in the United States as a precaution.

The questions raised by Donald's improvement are both simple and potentially significant: Did the gold-salts treatment alleviate his autistic symptoms, and if so, why?

Did the juvenile arthritis -- an autoimmune condition -- and the autism improve markedly at the same time because both were responses to a toxic exposure? Did the gold salts help pull mercury from Donald's body, and/or reduce an inflammatory immune response in his brain? Or is it all coincidence, or a memory blurred by the passage of 59 years?

Such questions, or course, are speculative, and some readers have criticized us for even asking them, given the assurances of the CDC and medical groups and the importance of immunizations in preventing infectious disease.

Wrote one reader over the weekend: "I can't morally just stand by and watch you exacerbate a situation where children are dying because fearful mothers didn't vaccinate. ... It is doubly sad when you consider that instead of your causing the deaths of children, you could have used your bully pulpit to do something good for autistic children."

But something good did seem to happen to one autistic child who was about to die: Donald T. All we're interested in is, why?

In the new year we'll look more closely at whether chelation and other treatments appear effective. First, though, we'll wrap up this review by recounting our efforts to find autism in U.S. children who have never been vaccinated.

--

E-mail: dolmsted@upi.com

A-CHAMP on Frist's tricks

From John Gilmore:

Well, Big Pharma won a round, sort of.

They couldn't win on the Senate floor. Think about that. A bunch of alert, angry and organized parents with about $134.98 collectively between us stopped S 1873, the number one priority of the $6 trillion pharmaceutical industry and the morally bankrupt leadership of the US Senate.

So Bill Frist used parliamentary tricks to at least salvage the liability protection the pharmaceutical industry so desperately wants. That's bad but not nearly as bad as it could have been. And S 1873 would have been far worse than what happened last night. If S 1873 had passed, vaccine development would have moved into the world of top secret weapons development. Revealing any information about a vaccine, except what the government wanted you to know, could have been proscuted as a terrorist act. It was possible under S 1873 that refusing a vaccine, or pandemic counter-measure, the new term for vaccines that Orwell would have been proud of coining, could have been prosecuted as a terrorist act.

What we all should have learned here is that it has gotten to the point where the pharmaceutical industry feels threatened by the basic institutions of democracy and is actively seeking to do away with them. This is not an exaggeration. They recognize that the Anglo-American sytem of justice, 1000 years in the making, no longer serves the short-term profit goals of a Swiss pharmaceutical giant, Novartis, and a French pharmaceutical giant, Sanofi Aventis, so it must go.

One wonders why the Soviet Union or Maoist China weren't at the forefront of vaccine development. Both countries had exactly what the vaccine industry wants: no liability, absolute secrecy, passive populations with no ability to resist the directives of the government, no free-market of goods or information, exactly the kind of world Paul Offit and the vaccine fascists are seeking to create. Except that under Khruschev thimerosal was evaluated as a preservative for vaccines and rejected as far too toxic for use in humans or animals. So I guess the Soviet Union was a little too soft for Offit.

And what have the pharmaceuticals got for their effort. Legislation that allows the President to declare a vaccine a pandemic counter-measure and give legal immunity to his buddies. The question is who would take the vaccine? The administration bombed once already with the small pox vaccine. And how much longer can they declare the sky is falling with avian flu? Remeber SARS? Remember the coming Ebola plague? It is just one more criminal act of a criminal gang that happens to be in control of Washington right now.

We on the other hand are better organized than ever and we will be back. We fought hard and we prevented something much worse than what happened last night from being unleashed. And we will be back.

December 22, 2005

Flu Vaccine-Makers' Liability Limited in U.S. Senate Measure

So Bill Frist got his liability protection for Pharma. Now if the avian flu breaks out and the government brings out the vaccine for it, pharma will not be responsible for any one who is injured by the vaccine. Will Pharma use this as the tip of the wedge to open up liability protection for all vaccine injuries? It is a safe bet.
Flu Vaccine-Makers' Liability Limited in U.S. Senate Measure

Dec. 22 (Bloomberg) -- Drugmakers would be protected from lawsuits related to flu vaccines under a $453 billion defense budget passed by the U.S. Senate.

The provision, added to the legislation last night by Senate Majority Leader Bill Frist, a Tennessee Republican, would require patients seeking to sue a drugmaker to prove the company engaged in willful misconduct when producing a vaccine. The measure fails to provide compensation for injuries or deaths related to a vaccine, said Senator Edward Kennedy, a Massachusetts Democrat.

``Generally around here we measure who the winners are and who the losers are,'' Kennedy said on the floor of the Senate. ``Drug companies come out time and time again, but never, never, ever, ever like they have with this sweetheart deal.''

The measure may benefit companies including French drugmaker Sanofi-Aventis SA, the largest supplier of U.S. flu vaccines, as well as London-based drugmaker GlaxoSmithKline Plc and the U.S. biotechnology company Chiron Corp., which are trying to develop a vaccine against avian influenza as governments try to prepare for a possible pandemic.

Kennedy said the liability waiver would be broader, covering vaccines related to any ``epidemic'' such as diabetes or obesity. As a result, the provision could apply to ``almost any vaccine, drug or device,'' Kennedy said.

The defense budget for the 2006 fiscal year passed after lawmakers removed a provision that would allow oil companies to drill in Alaska's Arctic National Wildlife Refuge. The legislation also includes $29 billion for reconstruction of New Orleans and Gulf Coast areas damaged by Hurricane Katrina and $3.8 billion for combating avian influenza that was added by Frist.

Frist AIDS Charity Paid Consultants

WASHINGTON - Senate Majority Leader Bill Frist's AIDS charity paid nearly a half-million dollars in consulting fees to members of his political inner circle, according to tax returns providing the first financial accounting of the presidential hopeful's nonprofit.

The returns for World of Hope Inc., obtained by The Associated Press, also show the charity raised the lion's share of its $4.4 million from just 18 sources. They gave between $97,950 and $267,735 each to help fund Frist's efforts to fight AIDS.

The tax forms, filed nine months after they were first due, do not identify the 18 major donors by name.

Frist's lawyer, Alex Vogel, said Friday that he would not give their names because tax law does not require their public disclosure. Frist's office provided a list of 96 donors who were supportive of the charity, but did not say how much each contributed.

The donors included several corporations with frequent business before Congress, such as insurer Blue Cross/Blue Shield, manufacturer 3M, drug maker Eli Lilly and the Goldman Sachs investment firm.

World of Hope gave $3 million it raised to charitable AIDS causes, such as Africare and evangelical Christian groups with ties to Republicans — Franklin Graham's Samaritan Purse and the Rev. Luis Cortes' Esperanza USA, for example.

The rest of the money went to overhead. That included $456,125 in consulting fees to two firms run by Frist's longtime political fundraiser, Linus Catignani. One is jointly run by Linda Bond, the wife of Sen. Christopher "Kit" Bond, R-Mo.

The charity also hired the law firm of Vogel's wife, Jill Holtzman Vogel, and Frist's Tennessee accountant, Deborah Kolarich.

Kolarich's name recently surfaced in an e-mail involving Frist's controversial sale of stock in his family founded health care company. That transaction is now under federal investigation.

Jill Holtzman Vogel, who is raising money for a run for the state Senate in Virginia in 2007, has received thousands in contributions this year from Catignani & Bond and from her husband, among numerous other sources, according to data released by the Virginia Public Access Project.

Alex Vogel said Frist picked people to work on his charity whom he trusted and knew, such as Vogel's wife, and was proud that overhead costs amounted to less than $1 of every $5 raised. "It's leaner than the average charity," Vogel said.

Frist is listed as the charity's president and his wife was listed as secretary. Neither was compensated.

Political experts said both the size of charity's big donations and its consulting fees raise questions about whether the tax-exempt group benefited Frist's political ambitions.

"One of the things people who are running for president try to do is keep their fundraising staff and political people close at hand. And one of the ways you can do that is by putting them in some sort of organization you run," said Larry Noble, the government's former chief election lawyer who now runs the nonpartisan Center for Responsive Politics that studies fundraising.

Kent Cooper, the
Federal Election Commission's former public disclosure chief, said the big donors' motives are also suspect.

"These tax deductible gifts were earmarked through Senator Frist," Cooper said. "They were raised in the political arena at the 2004 Republican Convention and the natural question is were they given to the Senate majority leader to gain favor or were they given for true charitable purposes?"

Cooper said the consulting fees were "excessively high" and the fact that they were "paid to primarily political consultants also raises questions about the long-range strategic benefits for the 2008 presidential race."

A charity could lose its tax-exempt status if it is found to be involved with political activity, said Marcus S. Owens, a former director of the
Internal Revenue Service's Exempt Organizations Division.

"If the IRS were to conduct an examination, what they would look for would be the relationship between the organization and any incumbent politician or candidate," Owens said. "They'd be particularly interested in transactions of money or assistance of any kind being provided."

Frist formed the charity in 2003. It drew attention in August 2004 when it held a benefit concert in New York during the Republican National Convention at which
President Bush was nominated for re-election.

The group's 2004 tax return was due April 15, 2005, but it filed for two extensions and only reported its activity to the IRS last month.

The tax forms show at least 11 of the charity's 18 biggest donors gave $97,950 each, that one gave $100,000 and that the rest gave more than $245,000 each.

Vogel said Catignani was paid the fees because he helped arrange the New York concert that featured country stars Brooks & Dunn, handling both the event arrangements and fundraising.

The tax forms show Catignani's fundraising firm, Catignani & Bond, was paid a total of $276,125 and his event-planning arm, Consulting Services Group, was paid $180,000.

The amount Catignani was paid by Frist's charity in 2004 is roughly the same as what his firms received over the past three years for work for Frist's political action committee, Volunteer PAC. The firm collected $523,666 in fees from the PAC since 2003, FEC records show.

World of Hope's beneficiaries include evangelical Christian groups with Republican connections.

Cortes, Esperanza USA's president, is an influential evangelical leader who hosted Bush at this year's National Hispanic Prayer Breakfast.

Frist has worked and traveled extensively with Samaritan's Purse in Africa as well as during the immediate aftermath of Hurricane Katrina. Franklin Graham is the son of the Rev. Billy Graham.

Weeks before Frist's convention fundraiser, the senate leader traveled to Chad, Sudan and Kenya on a trip underwritten by Samaritan's Purse, Senate records show.

Samaritan's Purse spokesman Jeremy Blume said the $490,000 that World of Hope donated to Samaritan's Purse in 2004 was spent on AIDS programs in sub-Saharan Africa.

The recipients of the charity's money were Africare, Samaritan's Purse, Esperanza USA, Nashville's Meharry Medical College, Taso-Uganda and Save the Children.

At Medical Journals, Writers Paid by Industry Play Big Role

Ghost Story
At Medical Journals, Writers Paid by Industry Play Big Role
Articles Appear Under Name Of Academic Researchers, But They Often Get Help

J&J Receives a Positive 'Spin'

By ANNA WILDE MATHEWS
Staff Reporter of THE WALL STREET JOURNAL
December 13, 2005; Page A1

In 2001, the American Journal of Kidney Diseases published an article that touted the use of synthetic vitamin D. Its author was listed as Alex J. Brown, an associate professor at Washington University in St. Louis.

But recently, that same article was featured as a work sample by a different person: Michael Anello, a free-lance medical writer, who posted a summary of it on his Web site. Mr. Anello says he was hired to write the article by a communications firm working for Abbott Laboratories, which makes a version of the vitamin D product. Dr. Brown agrees he got help in writing but says he redid part of the draft.

It's an example of an open secret in medicine: Many of the articles that appear in scientific journals under the bylines of prominent academics are actually written by ghostwriters in the pay of drug companies. These seemingly objective articles, which doctors around the world use to guide their care of patients, are often part of a marketing campaign by companies to promote a product or play up the condition it treats.

A HIDDEN ROLE?

Now questions about the practice are mounting as medical journals face unprecedented scrutiny of their role as gatekeeper for scientific information. Last week, the New England Journal of Medicine admitted that a 2000 article it published highlighting the advantages of Merck & Co.'s Vioxx painkiller omitted information about heart attacks among patients taking the drug. The journal has said the deletions were made by someone working from a Merck computer. Merck says the heart attacks happened after the study's cutoff date and it did nothing wrong.

The Annals of Internal Medicine tightened its policies on writer disclosure this year after a University of Arizona professor listed as the lead author of a Vioxx article in 2003 said he had little to do with the research in it.

The practice of letting ghostwriters hired by communications firms draft journal articles -- sometimes with acknowledgment, often without -- has served many parties well. Academic scientists can more easily pile up high-profile publications, the main currency of advancement. Journal editors get clearly written articles that look authoritative because of their well-credentialed authors.

Increasingly, though, editors and some academics are stepping forward to criticize the practice, saying it could hurt patients by giving doctors biased information. "Scientific research is not public relations," says Robert Califf, vice chancellor of clinical research at Duke University Medical Center. "If you're a firm hired by a company trying to sell a product, it's an entirely different thing than having an open mind for scientific inquiry. ...What would happen to a PR firm that wrote a paper that said this product stinks? Do you think their contract would be
renewed?"

Drug companies say they're providing a service to busy academic researchers, some of whom may not be skilled writers. The companies say they don't intend for their ghostwriters to bias the tone of articles that appear under the researchers' names.

Authors "have to sign off on everything," says Mark Horn, a Pfizer Inc. medical director. "This is properly viewed as a way to more efficiently make the transition from raw data to finished manuscript." Professors who get writing help generally say they give the writers input and check the work carefully.

The criticism of ghostwriting is one of several issues that have put scientific journals on the defensive. Even journal editors acknowledge they have sometimes done a poor job of detecting when articles cherry-pick favorable data to promote a particular drug or treatment. Some health insurers have stopped taking what they read in the journals on faith and are employing analysts to scrutinize articles for negative data that are buried.

It's hard to say how widespread ghostwriting is. An analysis presented at a medical-journal conference in September found that just 10% of articles on studies sponsored by the drug industry that appeared in top medical journals disclosed help from a medical writer. Often the help isn't disclosed. An informal poll of 71 free-lance medical writers by the American Medical Writers Association found that 80% had written at least one manuscript that didn't mention their contributions.

In the case of the vitamin D article, Dr. Brown says Abbott asked him to write it but he didn't have time. He had written an earlier article on the subject. "They said they would have one of their people write it, update my old review article and I would check it," he recalls. Mr. Anello, a Milwaukee writer who studied biochemistry at the University of Wisconsin, says he wrote the new article. "I've done a lot of ghostwriting jobs," he says, adding that sometimes he works closely with the named authors. (See related document excerpts.)

Dr. Brown says he had to rewrite "at least 30% to 40%" of Mr. Anello's draft. In retrospect, he says, he probably should have asked Abbott who Mr. Anello was and "if that person should be acknowledged." Abbott said the article's content was "under the complete discretion" of Dr. Brown and didn't discuss details. The journal's managing editor declined to comment because the journal is under new management.

Following questions from The Wall Street Journal, Mr. Anello removed the article summary from his Web site. Until recently, his online bibliography listed other scientific publications he has written under others' bylines that have yet to be published. The byline on one was "author to be named."

Medical writers frequently have scientific backgrounds. Some work for universities, drug companies or medical-communications firms, while others are free-lancers who typically get $90 to $120 an hour. A communications firm may charge $30,000 or more to have a team of writers, editors and graphic designers put together an article. Some of these firms are part of larger companies in publishing and advertising
such as Thomson Corp. and Reed Elsevier PLC.

Elsevier's Excerpta Medica unit helps clients craft publications for prestigious scientific journals. Elsevier itself publishes many such journals, most notably The Lancet. Excerpta Medica says on its Web site that its relationship with its corporate parent's journals "allows us access to editors and editorial boards." (See related excerpt.)

But Sabine Kleinert, an executive editor at The Lancet, says she has never worked with Excerpta Medica and rejects articles that have a marketing spin. "Promotion has a different goal than publishing a legitimate research study," says Dr. Kleinert. She suspects companies sometimes influence medical writers "to write it up in a certain way to make a product sound more efficacious than it is."

A 1999 document that turned up in a lawsuit describes Pfizer's publications strategy for its antidepressant Zoloft. The document, prepared by a unit of ad giant WPP Group, includes 81 different articles proposed for journals. They would promote the drug's use in conditions from panic disorder to pedophilia. (See related excerpt.)

Author 'to Be Determined'

For some articles, the name of the author was listed as "TBD," or "to be determined," even though the article or a draft was listed as already completed. Several of the listed articles ultimately ran in scientific publications -- including one in JAMA, the Journal of the American Medical Association -- without disclosing the role of outside writers.

In a statement responding to questions from The Wall Street Journal, Pfizer said agencies sometimes "pull together first draft manuscripts" based on information provided by researchers who will serve as authors. It says the academics who were later given credit as lead authors of the "TBD" articles were instrumental in designing the studies that the articles described. The lead authors said they had input into the drafts and approved the final papers.

In recent years, more journal editors have begun demanding that academic authors of studies explain their exact roles and disclose any work by medical writers. The editors say the writers can perform a valuable role so long as it's disclosed to readers.

Writers agree -- and the American Medical Writers Association is pressing for greater acknowledgment of its members' work. But some medical writers say they fear articles with full disclosure are likely to get bounced. Editors "say they want disclosure, but if you do it, they scream, 'ghostwriter!' " says Art Gertel, who oversees medical writing at Beardsworth Consulting Group in Flemington, N.J. "Despite the cries for transparency, the journal editors still feel that there's an element of corruption if a medical writer is paid by a drug company."

Catherine DeAngelis, JAMA's editor in chief, says even a conscientious journal can only go so far in policing academics. "I don't give lie-detector tests to people," Dr. DeAngelis says.

BMJ, a British medical journal, has one of the toughest disclosure policies, but it can get misled. Last year, a note at the end of a BMJ article on painkillers and asthma said the article was "conceived and initiated" by its three academic authors. Lead author Christine Jenkins "performed the analysis and drafted the paper," the note said, adding that the work wasn't funded by a drug company. Dr. Jenkins is a senior researcher at Australia's Woolcock Institute of Medical Research, which
has ties to the University of Sydney. (See related excerpts.)

In fact, a medical writer paid by GlaxoSmithKline PLC helped draft the manuscript, the drug company confirms. The analysis was almost identical to an earlier, unpublished one that the company says was "initiated" by that writer. Both analyses concluded that acetaminophen or Tylenol (sold under a different name by GlaxoSmithKline in Britain) was safer for asthma patients than aspirin or other painkillers. (See related excerpts.)

Dr. Jenkins says the structure of her work was "suggested" by the company version but she and the other authors did their own analysis. Dr. Jenkins says she personally "wrote a very large chunk" of the BMJ article and worked closely with the writer. Dr. Jenkins and GlaxoSmithKline declined to give the writer's name.

Dr. Jenkins says she didn't know that the company paid the writer. GlaxoSmithKline didn't pay Dr. Jenkins for the BMJ article, but the company previously paid her to speak at a conference and has given a major grant to the Woolcock Institute.

In a statement, GlaxoSmithKline says the paper "should have disclosed the involvement of a medical writer compensated by GSK." The company says it "regards the omission as a lapse on the part of GSK."

Fiona Godlee, BMJ's editor, says Dr. Jenkins "should have declared the involvement of the medical writer." Dr. Godlee says the journal will print papers that involve a medical writer, but she believes "the actual authors have to be incredibly closely involved."

When articles are ghostwritten by someone paid by a company, the big question is whether the article gets slanted. That's what one former free-lance medical writer alleges she was told to do by a company hired by Johnson & Johnson.

Instruction Sheet

Susanna Dodgson, who holds a doctorate in physiology, says she was hired in 2002 by Excerpta Medica, the Elsevier medical-communications firm, to write an article about J&J's anemia drug Eprex. A J&J unit had sponsored a study measuring whether Eprex patients could do well taking the drug only once a week. The company was facing competition from a rival drug sold by Amgen Inc. that could be given once a week or less.

Dr. Dodgson says she was given an instruction sheet directing her to emphasize the "main message of the study" -- that 79.3% of people with anemia had done well on a once-a-week Eprex dose. In fact, only 63.2% of patients responded well as defined by the original study protocol, according to a report she was provided. That report said the study's goal "could not be reached." Both the instruction sheet and the report were viewed by The Wall Street Journal. The higher figure Dr. Dodgson
was asked to highlight used a broader definition of success and excluded patients who dropped out of the trial or didn't adhere to all its rules.

The instructions noted that some patients on large doses didn't seem to do well with the once-weekly administration but warned that this point "has not been discussed with marketing and is not definitive!"

The Eprex study appeared last year in the journal Clinical Nephrology, highlighting the 79.3% figure without mentioning the lower one. The article didn't acknowledge Dr. Dodgson or Excerpta Medica. Dr. Dodgson, who now teaches medical writing at the University of the Sciences in Philadelphia, says she didn't like the Eprex assignment "but I had to earn a living."

The listed lead author, Paul Barré of McGill University in Montreal, says Excerpta Medica did "a lot of the scutwork" but he had "complete freedom" to change its drafts. Dr. Barré says he helped design the study and enroll patients in it. In statements, J&J and Excerpta Medica offered similar explanations of the process. J&J says it regularly uses outside firms "to expedite the development of independent, peer-reviewed publications."

A J&J spokesman said he wasn't familiar with the details of the instruction sheet and referred questions about the highlighted data to Dr. Barré, who said he never interacted with J&J's marketing department and doesn't believe the article was biased. He said the higher figure was "more representative" because those patients followed the study's rules. "Without wanting to distort data, you always want to put the spin that's more positive for the article," Dr. Barré says. "You're more
likely to get it published."

Hartmut Malluche, an editor of Clinical Nephrology, declined to comment on details of the article. The journal doesn't require authors to disclose the role of medical writers. But after hearing Dr. Dodgson's story, Dr. Malluche said he would suggest changing the policy. "It's not good if the company has control over the article," he says.

Some academics are protesting ghostwriting. Adriane Fugh-Berman, an associate professor at the Georgetown University School of Medicine, says she received an email last year from a company hired by drug maker AstraZeneca PLC. The email offered her the chance to get credit for writing an article. "... [W]e will forward you a draft for your input so that you would need only to review and then advise us of any changes required," it said.

She says she was shown a draft but declined the offer. Then the Journal of General Internal Medicine asked her to peer-review a version of the same article, submitted by a different researcher. She decided to go public, and wrote about her experience in the journal.

AstraZeneca and the communications firm say it was all a mistake. Dr. Fugh-Berman should have been shown a different article from the one she was later asked to peer-review, they say. The article for peer review was in fact written by the author who submitted it to the journal, they say. AstraZeneca says it "does not support the practice of ghostwriting" and always discloses any support it gives to academic authors.

John Farrar, a pain expert at the University of Pennsylvania, says he once turned down a company's offer to give him a ghostwritten draft about a study on which he had worked. "They said, 'That's unusual,' "Dr. Farrar recalls. He wanted to write the manuscript himself because "you can put your spin on it. ...The way it is written -- the way it's structured -- is yours."

Write to Anna Wilde Mathews at anna.mathews@wsj.com

Medical Journal Tests Reactions to Contact With Thimerosal

Contact Dermatitis
Volume 53 Page 324 - December 2005
doi:10.1111/j.0105-1873.2005.00591.x
Volume 53 Issue 6

Thimerosal – Is it really irrelevant?

Dan Slodownik1 and Arieh Ingber

Abstract:
Recently, several investigators claimed that thimerosal is one of the most irrelevant allergens existing in screening for contact dermatitis. 508 patients who were suspected to have allergic contact dermatitis were patch tested at our clinic. They completed a questionnaire including medical, demographic and occupational details. We used the standard tray of chemotechnique diagnostics (Malmö, Sweden) and additional series, which were case relevant. The relevance of the allergic reaction to thimerosal was scored from 1 to 6. 19 patients (3.7%) had an allergic reaction to
thimerosal. 6 (31.5%) had a definite relevance and 8 (42.1%) had a probable relevance. Only 3 patients (15.8%) had an irrelevant reaction. SPIN value (significance–prevalence index number) was 2281. We found a high proportion of mechanics (42.1%) among the patients who had positive reaction to thimerosal (P < 0.0001). Although previous reports found thimerosal highly irrelevant, our daily experience being supported by the above data indicates that positive reactions to thimerosal could be relevant for many patients.