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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:
You sure have some cute kids!
He's like a little cabbage patch doll! Awww. I feel so sympathetic that you and your family and other family's have to go through this. THere are people taking their health for granted, smoking and drinking poisoning their body. While there being children starving for that good health everyday.
Hi. I'm in Tennessee and just wanted to let you know that there are many of God's people praying for David throughout the world. We know that if we ask through faith, He will provide. God Bless!
My name is Cristina Moustirats. I am so impressed with what you have created as a WAS community and would like to collaborate with you. I lost my son, Sebby, to WAS last March and have recently started "The WAS Foundation" as a charity dedicated to this disease & the families that are faced with it. We are doing our first inaugural fundraiser Sept. 10th and I would love to talk to you.
Could you email me your contact info at cmoustirats@yahoo.com?
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