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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:
Hello Aimee-
I have tried to leave comments in the past, so hope this one is posted!
I just wanted to say what a beautiful tribute it was to your son on his 3rd birthday. It was very moving and expresses your love for him and your family.
I am sure your site is very helpful and informative for those in need.
Happy anniversary to you and Michael.
Our love,
Dale and Joan
Hi, Aimee!
I absolutely LOVED your slide show of David! It was beautiful!!
So glad you and Michael got to celebrate your 10th anniversary together! Looks like you had a wonderful time!
Blessings,
Andrea Marley
Hi Dale and Joan! Yes, it worked for you this time. Thanks for reading the blog. I wish we could see each other more often.
Hi, Andrea! It's such a blessing we had time to get away. As you know, things can change so quickly when you have a sick child. I'm thankful we were given the opportunity to celebrate. Miss you!
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