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Article: Should Severely Disabled Kids Be Kept Small?

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Nikolita
Captain

PostPosted: Sun Nov 05, 2006 9:49 pm


Taken from: http://msnbc.msn.com/id/15517226/

NEW YORK - In a report published in a medical journal this month, two doctors describe a 6-year-old girl with profound, irreversible developmental disability who was given high doses of estrogen to permanently halt her growth so that her parents could continue to care for her at home.

The controversial growth-attenuation treatment, which included hysterectomy, was requested by the child's parents and initiated after careful consultation and review by an ethics committee.

In their report in the Archives of Pediatrics and Adolescent Medicine, Drs. Daniel F. Gunther and Douglas S. Diekema, both at the University of Washington in Seattle, explain the reasoning behind what they hope will generate a healthy debate. Gunther is at the Division of Pediatric Endocrinology, and Diekema is at the Center for Pediatric Bioethics.

Caring for children with profound developmental disabilities can be difficult and demanding, they note. For children with severe combined neurologic and cognitive impairment who are unable to move without assistance, all the necessities of life — dressing, bathing, transporting — must be provided by caregivers, usually parents, and these tasks become increasing difficult, if not impossible, as the child increases in size.

"Achieving permanent growth attenuation while the child is still young and of manageable size would remove one of the major obstacles to family care and might extend the time that parents with the ability, resources, and inclination to care for their child at home might be able to do so," Gunther and Diekema write.

The parents of the 6-year-old, both of whom were college-educated professionals, indicated a strong desire to continue caring for their daughter. Despite having the neurologic development no greater than that of an infant, the 6-year-old responds to her parents and two healthy siblings — vocalizing and smiling in response to care and affection — and "clearly is an integral, and much loved, member of the family," the authors note.

After extensive evaluation, the combined opinion of a team of specialists is that the child will have no significant neurologic or cognitive improvements.

The onset of puberty and continued growth caused concern in the parents about how they would care for their daughter long-term, which they clearly wanted to do. They were concerned about having to turn over care to "strangers" and also about the complications that would arise when the child started menstruating.

The child is now a little more than a year into growth-attenuating therapy and approaching the end of her growth, Gunther and Diekema report. "As of yet, there have been no treatment complications."

The authors feel that growth arresting therapy can be "both ethical and feasible and should be an option available to parents."

The authors of a commentary applaud Gunther and Diekema for publishing this case report, although they believe that attempts to attenuate growth are "ill advised."

Nonetheless, Dr. Jeffrey P. Brosco from the University of Miami and Dr. Chris Feudtner from the University of Pennsylvania, Philadelphia, say that by beginning the debate, this paper helps to "advance our ethical dialogue as we struggle to define our core values in words, laws, and deeds. Only with further research and public discussion will we learn whether attempts to attenuate growth run with or against our fundamental values in caring for children with profound developmental disabilities."
PostPosted: Fri Dec 08, 2006 4:47 pm


Hmm, this is a tricky one.

I completly understand where the parents are coming from. With someone as severly disabled as that caring from them if they are much smaller (ie, a child) would greatly reduce many struggles they'd have if the child did grow.

I think it may actually be good for the child too, as the parents will be fully capable of caring for them pretty much on their own without much extra need for support. Having strangers around can be very upsetting for people of that state.

An awful point to mention, but the cost of such treatment will probably outweigh cost as the child grows. For example, specialist equipment for adults rather than children (hoists, bath quipment, whelchairs etc etc) wouldn't become an issue if the child was not to fully physically develope past childhood.

Obviously there is the ethical issue, as to whether such tampering with a person who cannot truly give a desicion is right or wrong. But the above factors and more must be taken into consideration.

Of course, with the example child being female, the stopping (well, not starting) of menstruation will reliev an enormous amount of pressure on the family, and on the child herself. I am unsure as to whether they (the child) would be aware of what was going on physically with their body or not. The stopping of menstruation happens in many cases such as this, although not with the anti growth involved.

Also, by relieving (paid or voluntry) careworkers of the need to greatly assist such a family, they have more time and energy available to assist other families whom need help.

I personally think it's a good thing, overall.

Modified Mummy


Savina

PostPosted: Fri Dec 08, 2006 11:00 pm


Argh, hard topic for me.
I personally feel that if someone is so disabled that they need constant medical care and can't walk, talk, breathe or eat on their own that they should be allowed to die. I believe in quality of life over quantity.

So really with this story, it's a six year old with the abilities of a four month old. Hmm. Obviously will never be a functioning member of society. If they want to keep caring for her, sure, it's easier to have her small than lug around a 100 lb. vegetable.
PostPosted: Thu Dec 28, 2006 11:27 pm


Yes, exactly. A human who cannot care for themselves at all should be allowed to die. I have told my family that if ever i am in a car crash and i am a human vegetable, much like these disabled people that i wish to die. On the upside at least these disabled people don't understand what is going on.

Laura_Ingalls


lunashock

PostPosted: Sat Dec 30, 2006 5:20 pm


While I agree on the whole quality of life thing, doctors are, for lack of a better term, pessimists. You really can't gauge how bad some conditions are going to be in utero.

One of my godchildren has William's Syndrome. He's probably on the level of a 4 year old, MAYBE. He needs constant care and will never be high functioning enough to live on his own. He can walk and use the bathroom fine, but when he was born they gave her a MUCH graver scenario than he is in now. He is a total gem to be around, albeit a lot of work.

Some conditions are really hard to gauge initially. I know this particular circumstance, the 6 year old has the capacities of an infant, but I just wonder what extent this treatment ranges to?
PostPosted: Thu Jan 11, 2007 1:52 pm


I have done some reading on the specific case of ashley the little girl. To be honest now that i have read her families personal blog and letters from others i understand why they chose to giver her the "ashley treatment" The hormone therepy was actually used quite often years ago when tall women werent considered as attractive as small ones. The only risk it poses is a higher chance of cervical cancer, and premature puberty. They chose to give her a hysterectomy because apparantly in disabled women the change of hormones and just the challenge of keeping a women clean there causes infections and mental function to cease. The final preocedure they chose for there daughter was to get her breast buds removed becuase large breasts run in her family and they didnt want her to be sexualized by a caregiver and also for comfort purposes. They change her postion often so she doesnt get bored including lying on a pillow propped on her chest. They did several other things just to protect her future health......including getting tubes in her ear to prevent ear infections, and getting her appendix removed as she would not be able to tell them other than crying if she was feeling pain there. they did all those things so she could stay at home with them and not have to ever be put in a home because they couldnt care for her. Reading there blog made me rethink my veiws because originally I was totally against what they did.


here is the link to the blog so you can all form your own opinions on her case in particular.
http://ashleytreatment.spaces.live.com/blog/

i think the fact of the matter is that every person in different and sometimes the things they need seem crazy to everyone else.

wotfan


The_Vampress

PostPosted: Mon Jan 14, 2008 11:52 pm


Savina
Argh, hard topic for me.
I personally feel that if someone is so disabled that they need constant medical care and can't walk, talk, breathe or eat on their own that they should be allowed to die. I believe in quality of life over quantity.

So really with this story, it's a six year old with the abilities of a four month old. Hmm. Obviously will never be a functioning member of society. If they want to keep caring for her, sure, it's easier to have her small than lug around a 100 lb. vegetable.
what I would say too.

quality of life is supremely more important than quantity.
PostPosted: Tue Jan 29, 2008 12:45 pm


Well, good job and good luck for parents or people that want to look after someone disabled especially that much. I would never be able to do it.

If I had a child and they were disabled I'd have to either give them up for adoption or I'd want them to die so they won't have to live life poorly. O_o
Likewise, if something ever happened to me, I probably wouldn't want to live either. ^^';

Fiaroka

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