Thirteen years ago, Braxton was diagnosed with this rare genetic disorder. We did not know what the future would hold, but the IWSA put us in touch with families like ours. We learned that our kids do have an unlimited future of possibilities. Today Braxton is a 4.0 student and thrives and excels at all he does. He exceeds all of our expectations everyday.
Supporters are now helping to
By liking our page, the IWSA can become more visible, thereby creating more opportunities for families around the world with WAGR/11p Deletion to find the support they need from other families who have "been there".
We are fundraising for International Wagr Syndrome Association. Join us in supporting them.
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