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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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Hi! My name is Paige Robins and my 4 1/2 month old son was diagnosed with WAS about a month and 1/2 ago. I've been putting updates on Facebook, but to make them more easily accessible, I just started a blog (www.weloveayden.blogspot.com). Thank you for writing about your experience. It's really helpful to read about it.
Thanks for responding! I hope you don't mind that I put the link to your blog on mine. These blogs have been SO helpful and encouraging that if anyone finds mine, I want them to be able to find others relatively easily as well. It's so great to read about babies and little boys doing at least fairly well after a BMT. It's a little terrifying being on this side of it. I really appreciate you helping me get in touch with other people. It seems like everyone else I talk to has a different experience, but so far, they've all been mostly positive.
Thanks again! Your family is beautiful, by the way. :-)
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