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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:
Hi Aimee,
Time has indeed flown by. The girls look so tall and grown up. You look great too. Five days post....I hope that you get to hold this little guy in your arms soon!
I hope the David's hands feel better and he can do things with his sibs.
Aimee, I am putting together a website for WAS and one section has links to a few family WAS web pages that I know. Is it okay with you if I add a link to David's page?
Thanks Aimee and take care.
Sumathi
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