Tuesday, September 11, 2007
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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
2 comments:
Hi, Aimee!
Just catching up on your blog, and so glad to hear you have the okay for Sea World! David will love it!!! And so will all of you! Hope you get to go soon!
Sorry to read about your recent scare with the iron pills! How scary! So glad everything turned out okay!!
I would have loved to have participated in the blood drive, but had a date with me daughter that day. I hope you had a great turnout!
Lets try to figure out when we can do our scrapbooking date!
Blessings,
Andrea
Hi Aimee,
We're really glad to have found your blog. David could be our 15 month old son Peter. They have so many similarities. We're currently familiarising ourselves with BMT which has just been suggestesd to us as an option. Like David, Peter's only symptom is low platelet count (most recently 15K). One query - David's helmet looks great, could you let us know where you got it from? We have a softtop but David's looks better. Back to your blog to keep reading, thanks.
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