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Wednesday, May 19, 2010

“Doctor at center of autism/vaccine scare expects to ... - Austin American-Statesman” plus 2 more

“Doctor at center of autism/vaccine scare expects to ... - Austin American-Statesman” plus 2 more


Doctor at center of autism/vaccine scare expects to ... - Austin American-Statesman

Posted: 19 May 2010 10:30 AM PDT

Home > Salud > Archives > 2010 > May > 19 > Entry

Doctor at center of autism/vaccine scare expects to lose license but will keep research in Austin

Dr. Andrew Wakefield — the British doctor who came to Austin after fueling a worldwide scare over vaccines and autism — said that he fully expects to have his British medical license yanked next week in a final effort by the mainstream medical establishment "to silence me and stop the research."

The General Medical Council in January found Wakefield guilty of acting dishonestly and irresponsibly in researching children with autism in England and writing a 1998 paper in the prestigious Lancet journal that was ultimately retracted in February. The council also said Wakefield showed "callous disregard" for children at his child's birthday party in 1999 when he had blood taken from them, paying them about $10 each and later joking at a conference about it.

In his first in-depth interview since the council's findings, Wakefield, who headed the Thoughtful House Center for Children in Austin until he resigned in February, said the charges were unfair and false and he does not intend to fade away. He is coming out with a book Monday, the same day he expects the council to take his license, called "Callous Disregard," to give his side of the story. He also intends to continue his research into the potential link between vaccines and autism, including gastrointestinal problems in children with autism. He plans to do that work in Austin with Dr. Arthur Krigsman, who also, until recently, practiced at the Thoughtful House.

What the council will finish Monday "has been done for the specific purpose to silence me and stop vaccine safety research," Wakefield, 53, said. "Vaccine safety is built upon the confidence of the public… and I'm not prepared to (compromise) that."

Wakefield did not have a license to practice medicine in the U.S. but headed the research program at Thoughtful House, which treats children from around the world.

You can read more about what Wakefield had to say in the Statesman tomorrow.

Permalink | Comments (4) | Post your comment Categories: Autism

Comments

Austinites love to be heard, and we're giving you a bullhorn. We just ask that you keep things civil. Leave out the personal attacks. Do not use profanity, ethnic or racial slurs, or take shots at anyone's sexual orientation or religion. If you can't be nice, we reserve the right to remove your material and ban users who violate our Visitor's agreement. Click here to report comment abuse.

By Famous Original Bob

May 19, 2010 1:06 PM | Link to this

"he does intend to fade away"

I hope that's a typo.

By todd

May 19, 2010 1:33 PM | Link to this

It's funny how many Austinites still think there is a link to Autism and vaccines. They care more about their false idealism than the health of their children.

By Texas sends babies blood to Transelvanyia

May 19, 2010 1:58 PM | Link to this

Anyone besides me notice the irony of little kids volunteering their blood for a study for $10 versus the new born babies who are stuck in the foot at the hospital for the same reason by the STATE without parental consent or notice?

By YeahRight

May 19, 2010 2:04 PM | Link to this

"Foreward by Jenny McCarthy"

I've read enough already!

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Autism's effect on the 'normal siblings' - NorthJersey.com

Posted: 19 May 2010 10:44 AM PDT

When Gabby Abramowitz was younger, she was cautious about inviting new friends to the house. She wasn't sure how they would react to her younger brother, Ben, who is autistic.

And she didn't want a repeat of the Simpsons incident. That was the time she had a friend over for dinner, and Ben sat at the table reciting the entire "Treehouse of Horror" Simpsons Halloween special.

Gabby pleaded with him to stop, but he persisted.

"My friend was like, 'What's going on?' and then started laughing," she said.

At that time, she was in elementary school and lacked the words and understanding to explain her brother's condition. But with the help of her parents and through her own study, Gabby, now 16 and a sophomore at Tenafly High School, has grown to understand the nuances of autism and often speaks out to teach her peers while growing closer to Ben, 14.

Through her research, she found that her experiences, and those of others like her, often are overlooked. "I think the effect on siblings is underestimated. We get pushed into the background."

Last year, she embarked on a year-long, independent research project on the topic, interviewing experts, authors and siblings of autistic children, including a family in Utah. The project was prepared for a national gifted education program called ROGATE (Resources Offered in Gifted and Talented Education) and she presented her findings at a regional gathering of high schools at Montclair State University.

The project did not end there. To obtain the highest honors from the ROGATE program, she had to apply her research to the community. In February, she organized a charity knockout basketball game at Tenafly High School, raising $650 to donate to the Post-21 Club of Bergen County, a non-profit serving those with autism who are too old for school programs.

In her research, she found echoes of her own life. In interviews, she heard from others who said being the "normal" child left them feeling frustration, guilt and neglect. That shared experience inspired her to create a teen-run sibling support group. In mid-March, she convened the group for the first time with two other Tenafly High School teens whose siblings are autistic.

Diane Schulthes, the middle school's coordinator for gifted and talented programs, who sat in on the group, was impressed with the students' ability to connect. "Gabby ran the whole meeting by herself. She started with open-ended questions and asked how they deal with kids making fun of their brothers or sisters. At the end, they thanked her. I was invisible at that point."

As much as Gabby is precocious, Dr. Sandra Harris, executive director of Rutgers Douglass Developmental Disabilities Center, said her quest is fairly typical. "One of the major challenges for these folks is trying to understand themselves in relation to their siblings, what it means to their lives, and their parents' expectations of their relationship to the sibling," said Harris, author of "Siblings of Children With Autism: A Guide for Families."

With just 20 months between Gabby and Ben — they have an 11-year-old brother, Gideon — much of her childhood was shadowed by Ben's condition and her parents' determination to find him the best treatments available. "We tried everything under the sun. We were making sacrifices," said Lisa Abramowitz, their mom.

Gabby remembers being annoyed at the frequent weekend trips to Baltimore to join her mom and Ben, who stayed in Maryland for weeks at a time so he could undergo a special auditory therapy. "It was before I understood what was really going on. I felt like my brother was getting all this attention from my parents," she said.

She also feels frustration with her peers when they make ignorant remarks about autism. When out to dinner with friends, one asked, "What special foods does he have to eat?" Gabby said she nearly spit out the water she was drinking. "I was speechless," she said. "I try to make them understand it's a social disability."

Having an autistic sibling can make teens like Gabby grow up much faster than their peers. She has already decided that she will be looking out for Ben when their parents can't care for him anymore. "I'm willing to help, because even though my brother is 'different,' he's still my brother, and I still love him just as much," she writes in the personal reflection section of her ROGATE research presentation.

For now, she's looking forward to keeping a close eye on him when he joins her at Tenafly High School next year. Ben, who has a high-functioning form of autism, was able to enroll in mainstream public school classes starting in the second grade. His most recent diagnosis is Asperger's syndrome.

And Gabby, a social butterfly, found a way to connect with Ben through sports. A die-hard sports fan and a Yankee loyalist to the core, Ben can recite sports statistics faster than you can type into Google, "How many wins did the Yankees have in 2009?"

"138 — combining the regular season, spring training and playoffs" said Ben.

Gabby often parks on the couch and watches baseball with her brother. "He gets very into it and cries when the Yankees lose. I tell him, 'Ben it's just a game. They'll win next time.' "

E-mail: fujimori@northjersey.com

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Fairfax: Autism, not 'baby boomers,' biggest future ... - Washington Post

Posted: 18 May 2010 08:58 AM PDT

The wave of aging "baby boomers" needing public health services in Northern Virginia -- once thought to be the greatest healthcare and fiscal threat facing local governments in the coming decades -- will be far outnumbered by the skyrocketing percentage of young adults with autism diagnoses, Fairfax County human services officials said Tuesday.

According to statistics compiled by the Fairfax County Public Schools, 1 in 83 enrolled students are now diagnosed with some form of autism, an 846 percent growth since 1997.

"That is a niche that's not being covered and those families are struggling," said Board of Supervisors Chairman Sharon Bulova (D).

Pat Harrison, a deputy county executive in Fairfax overseeing human services programs, said the county's 65-and-older population will reach 138,000 by 2020, but that the population of young adults with autism is growing at a far faster rate.

To help, Fairfax is partnering with the state and private agencies to create a pilot day program for young adults with autism. But respite services, reliable transportation, housing and recreation and vocational training programs are in dire need, officials said.

"The autism wave is going to be far more challenging. ... We need to begin to have discussions on how to deal with it now," Harrison said.

Many Northern Virginia communities with high numbers of children have rallied together in recent years and lobbied lawmakers in Richmond to mandate state health benefits for sometimes-pricey autism treatments.

By Derek Kravitz | May 18, 2010; 12:03 PM ET
Categories:
Fairfax County | Tags: Board of Supervisors, Fairfax County, Fairfax County Public School, Fairfax County Virginia, Northern Virginia, Pat Harrison, United States, Virginia  
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The country, not just Fairfax County, is facing the same tidal wave.

The real tragedy is that evidence is growing that gestational and early childhood vitamin D deficiency is the environmental trigger for autism, as outlined in a recent Scientific American Article. Three Swedish papers were published in March in support of the theory and recently, Professor Kinney and four other Harvard researchers accepted and modified the vitamin D theory in a paper in Medical Hypotheses.

If true, the tragedy is more poignant in that physicians and parents can easily prevent the disease with adequate daily doses of vitamin D.

More importantly, vitamin D's mechanism of action, which is epigenetic, implies a treatment effect in children already diagnosed.

John Cannell, MD
Vitamin D Council

Glaser G. What If Vitamin D Deficiency Is a Cause of Autism? Sci Amer April 24, 2009.
http://www.scientificamerican.com/article.cfm?id=vitamin-d-and-autism

Fernell E, Barnevik-Olsson M, Bågenholm G, Gillberg C, Gustafsson S, Sääf M. Serum levels of 25-hydroxyvitamin D in mothers of Swedish and of Somali origin who have children with and without autism. Acta Paediatr 2010 Mar 5.

Eyles DW. Vitamin D and Autism, Does skin colour modify risk? Acta Paediatr 2010 Mar 8.

Humble MB, Gustafsson S, Bejerot S. Low serum levels of 25-hydroxyvitamin D (25-OHD) among psychiatric outpatients in Sweden: Relations with season, age, ethnic origin and psychiatric diagnosis. J Steroid Biochem Mol Biol. 2010 Mar 7.

Kinney DK, Barch DH, Chayka B, Napoleon S, Munir KM. Environmental risk factors for autism: do they help cause de novo genetic mutations that contribute to the disorder? Med Hypotheses 2010;74:102-6.

Posted by: jjcannell | May 18, 2010 7:16 PM | Report abuse

Keep these comments coming. THIS is the point we have been trying to make in the Virginia legislature only to be rebuffed over and over.
The Virginia Autism Project in partnership with Autism Speaks has proposed insurance reform for autism treatment in Virginia. Intensive early intervention improves the outcomes for people with the diagnosis of autism. Ultimately costing taxpayers less.
To do otherwise is foolhardy and as stated above will cost more than anyone can imagine. Eighteen other states (maybe 20 by this week) have passed this legislation. Let's not be the state that covers erectile dysfunction drugs for state employees but NOT autism treatment and therapy for it's children.

Posted by: teechamp | May 18, 2010 10:04 PM | Report abuse

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