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My son had a mild common mutation of Wiskott Aldrich Syndrome (WAS). We decided, after 2 years of research, to not do the BMT but one month after our decision, he had a brain hemorrhage from jumping on a trampoline. His hemorrhage was treated with platelets but we were quickly encouraged to do the BMT. When he was two yrs old, he had a BMT with a 10/10 unrelated adult donor. We hope our research will help other families struggling with WAS. Feel free to email me: aimeemcnally@gmail.com
1 comment:
Fascinating
I have known for a long time that you can't fix something unless you first know how it is supposed to work.
Sounds like this research is moving quickly to discover that new knowledge and understanding. :-)
That is very encouraging.
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