A TWIST OF FATE-ATS, NONPROFIT FOR ARTERIAL TORTUOSITY SYNDROME
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The Alba Carter Foundation is an non-profit started by Alba's family when they learned what it was like to be in the hospital and faced some very scary times with their daughter Alba, when she received a heart transplant, due to Turner's Syndrome.  They wanted a way to give back and so with the Alba Carter Foundation, they can.  Click here to learn more about what Alba Carter and her fearless family are doing, and you can even follow them on Facebook by clicking, here.

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Arkansas CHD Coalition is a network of Congenital Heart Defect patients (of all ages), their parents, families, and medical care providers here in Arkansas bonding together to help support each other; to support other organizations with similar goals; and to organize awareness and fundraising events for CHD causes. We provide a venue in which to connect and share our cause, information and suggest...ions across the state. We also strive to provide awareness and education regarding Congenital Heart Defects: the needs, the struggles, the joys, and the future


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The goal of Greyson's Advocates is to provide information and materials to families of children facing significant medical diagnoses or extended hospital stays in an effort to allow them to focus on being advocates for their children. This will primarily be achieved through distribution of the Greyson's Advocates Medical Journal and hospital gift bags. The Medical Journal will help families keep all relevant medical information in one location, and provides a historical record of a child's medical procedures. Hospital gift bags will include toiletries, snacks, and other items which may be useful to families while in the hospital. When possible, Greyson's Advocates will connect families with other organizations that may be able to help with their specific needs.

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  • Home
  • About A Twist of Fate-ATS
  • Research and News about ATS
  • ATS Events
  • Our Friends
  • Contact