Supporting the Fight Against Mitochondrial Disease
About Us
Who are we?
This foundation was created in honor of our beloved sons and brothers...Cooper and Cash, to help fund research for treatment for Alpers disease. Alpers is a rare mitochondrial disorder that affects major organs of the brain, eyes and liver.
Our younger son Cash was a healthy 1 year old when he started to go into liver failure, which is when we discovered he had this disease. Cash was able to get a liver transplant which allowed his life to be prolonged a few more years before he went home to heaven.
Through the transplant process, Cash had severe brain trauma as a result of Alpers, which made him lose the ability to control his legs and arms. But we believe that he is in heaven now with a fully functioning body, running on those streets of gold, which is the foundation for this organization.
Cooper, with heartfelt loss, was welcomed into heaven by Cash the end of November 2022, days after his 11th birthday. These losses have devastated our family, but if we can do anything in this life that we have left, we hope to raise awareness and encourage others that are struggling on this side of heaven. Please join us in our support!!
What we are doing!
Our primary beneficiary is the Children's Hospital of Philadelphia's Mitochondrial Medicine Frontier Program, which is the world's foremost program on Mitochondrial Disease Research.
This year we are looking to expand our local support and reach out to other families in need in addition to supporting research at CHOP.
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If sponsoring, please email me at Streetsofgoldfund@gmail.com or text me at 804-873-6479 and I can get you setup with our sponsorship form for your tax purposes.