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Daily Digest Archive for February 20, 2003

Q: (Initially posted on February 17, 2003) FROM MENTEE BRITTANY. T. IN CA
My family is looking into adopting a child that social workers say may have experienced some oxygen deprivation at birth. He does not show any physical deformities but at 6 months has not begun to sit up. Could this be related? What types of problems could he face in the future? How can we determine if any of these problems are present now?

February 20, 2003
A: FROM MENTOR JOAN LUSK IN RI
You face a serious situation and a difficult decision. You definitely need to get the best medical assessment and advice that you can. Enough oxygen deprivation can cause brain damage - but how much is enough, and how much damage does it take to disable a person? At how early an age would damage become apparent, and if a baby's development is slow does that mean he'll never reach a normal level? And which abilities are most likely to be impaired? Are there any reliable tests of brain function now that can predict adult capabilities? I rather doubt that there are - perhaps a doctor among us knows.

You are justified in being concerned, given the report of possible oxygen deprivation. But what proportion of eventually normal people are slow to sit up? I don't even know whether 6 months is terribly late. Lots of bright people are slow to speak and to develop motor functions. It seems to me that you need not only the average developmental progress but a sense of the range of normal limits. http://www.nhsdirect.nhs.uk/SelfHelp/info/advice/normalchilddevelopment.asp gives an authoritative schedule for normal development, and says that at six months it's normal to _try_ to sit up, and at one year a child should be _able_ to sit up - so it seems by this criterion alone this child may be perfectly OK. Another site claims that at six months it _is_ normal to sit up. I take the discrepancy to mean that there is a range of normal ages for this developmental event. As the latter site says, "All children do the same things, but not at the same time."

I don't think there are absolute predictions to be found with medicine in its current state - but you should try to get the best answers you can. We each have limits to how much care we are willing and able to give another person - but it seems that those limits turn out to be a lot higher in most people than they would have predicted before being faced with the challenge. Caring for a disabled child, though, can be very very hard on a marriage or a family. You find examples where everyone concerned pitches in and finds the task spiritually rewarding - and other examples of families breaking up under the strain.

This past Sunday's New York Times Magazine had a provocative article by Harriet McBryde Johnson , a physically disabled lawyer, who accepted an invitation to debate Princeton philosopher Peter Singer on the right of disabled people to live. Johnson is clearly very smart; it's her muscles that don't work, not her brain. But you may find the issues very relevant, I think. The matter reduces to whether anyone has the right to decide another person's "quality of life" is too low to carry on.
http://www.nytimes.com/2003/02/16/magazine/16DISABLED.html



 

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