Day -7
We are counting down to day zero, which is when the BMT happens. Today was Day -7. Tomorrow will be Day -6. Once we get to Day zero, we will start to count up.
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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
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I've been checking in when I can. I am glad David appears to be doing well. Hope Mama is the same.
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