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This fundraiser ended on 07/07/12

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Supporting Kasan with medical travels and chromosome awareness!

Kasan was diagnosed with 49 Chromosomes 2 years ago. Since then we have traveled all over Montana, San Francisco, Spokane and all the way to Baltimore, Maryland to seek medical consult and to continue his treatment plan. July 2012 Kasan is going back to Maryland for further evaluation and education for his disorder. Kasan is the only "known" case in the State of Montana. That is why the resources are further away. The doctors in Baltimore (and he sees approximately 3 this time) are the only ones currently that have the 40+ patients known to have the disorder that are focusing on the findings and sharing with us to develop and better Kasan's treatment plan. And because we are blessed with so much love and support we want to share this cause with Montana! For Kasan, we have also wrote a letter to the Governor of Montana, and we were granted May as X & Y Chromosome Variations Awareness Month to bring awareness to Montana families! With Kasan's fundraisers he will also be sharing his chromosome information and importance of testing. Thank you for your help to make all of this possible for Kasan!
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