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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
4 comments:
We will continue with our prayers as we know Our Father is here for us. Thanks for the site so we could stay connected. We love you, Betty and Larry
Dear Michael and Aimee,
Little David is in our prayers. We love you and care for you and your beautiful family. Herb & Luanna
Hi Aimee,
I am Sumathi. Ramya(Varun's mom) just mailed me your Blog and my heart just goes out to you. NIH is a good place to go. They give such sensible advice.
My son has XLT(mild WAS) and has an exxon 2 missence also.He is now almost 7 years old and we have not transplanted him. He is a very happy kid. His plt are only 20,000. I would love to get in touch with you as it is so rare to find XLT's. You can e mail me at sumathidoc@aol.com
Michael and Amy,
You have been and continue to be in our thoughts and prayers. We love you and your wonderful family.
Joy and Bill
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