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Archive for the ‘OCD’ Category

Writer: ‘Misperceptions, prenatal screening threaten diversity’

Sunday, May 25th, 2008

Stephanie Meredith, past co-president of the Down Syndrome Association of Atlanta, sends a response to Leslie Roberts’ blog post: ‘When abortion may be an acceptable choice.’ Roberts, a Canadian newsman and television personality, had written that abortion may be an acceptable choice when a disability is diagnosed prenatally.

Meredith writes:

Far from adding unendurable stress, parents of children with Down syndrome indicate that the stress involved with raising a child with Down syndrome is lower than expected (Hodapp et. al. 2001) and that families enjoy positive benefits from raising a child with Down syndrome (Blacher & Baker 2006). In fact, research suggests the parents of children with Down syndrome actually experience a lower divorce rate than couples who do not have children with Down syndrome (Urbano & Hodapp 2007), and the siblings of children with Down syndrome are typically more compassionate and well-adjusted than their peers (Dykens 2005).

While the reasons for this have not been fully explored and since most parents would resolutely deny the claim that they are saints, the evidence suggests that there is something to be learned from embracing genetic diversity. (more…)

Restaurants, OCD a volatile mix

Wednesday, February 6th, 2008

Writing in the New York Times, broadcast journalist Jeff Bell explains what it’s like for a person with obsessive compulsive disorder to go to a restaurant. Thanks to a therapy called exposure response prevention, Bell is now able to visit restaurants without being immobilized by fears, anxieties and repetititive behaviors.

I am no brain scientist. I understand almost nothing about proteins and neurotransmitters. But my own extensive work with this particular form of torture (that is, directed treatment), with medication, has progressively allowed me to take back much of the life my disorder stole from me.

Today I travel extensively, sharing my recovery story and working with groups like the Obsessive Compulsive Foundation to raise awareness. In my job as a radio news anchor, I don’t have to eat out much, but when I’m on the road for work related to the disorder, I wind up eating in a lot of restaurants. I can honestly say I’m starting to enjoy it. In fact, while I still like ice water with my meal, I often find myself drinking from the glass, not washing with it.

Now when I say check, please, I’m simply asking for my bill.

Bell is the author of the book “Rewind, Replay Repeat.”

From the in-box

Tuesday, July 31st, 2007

20070731_john-roberts-swe.gif

John and Jane Roberts at his swearing-in ceremony in 2005. (AP Photo)

– Doctors have started using the word “epilepsy” in connection with Chief Justice John G. Roberts Jr. , who stayed overnight in a hospital in Maine after experiencing a seizure on Monday. The seizure was similar to one he experienced 14 years ago, according to a court press release.

– Parents of children with disabilities send a few choice words in response to a recent Wall Street Journal story on special ed — words like “union thugs” and “overpaid fat-cat administrators.”

– Researchers find a link between pesticide exposure and autism, but caution that it’s too early to draw conclusions.

– Reviewing the new reality series “Flipping Out,” Ginia Bellafonte says the show at last sets the record straight on obsessive compulsive disorder.

“For years now, the comic detective series “Monk” has equated O.C.D. with intuitive brilliance. We’ve long required a corrective interpretation, and “Flipping Out” is it. Mr. Lewis isn’t a genius of anything. He’s just a delusional jerk.”

– A growing number of professionals are prescribing a new treatment to patients with depression and anxiety. They call it “bibliotherapy.” In lay language, that means: read a self-help book.

About the Blog

More than 50 million people in the United States have disabilities, a number that is growing rapidly as the population ages. Experts say disability will soon affect the lives of most Americans. This blog attempts to explore what we know about disability, and to chronicle the efforts of people who are seeking new ways to address familiar challenges.

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