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PMLC MEF2C Awareness




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The MEF2C Association was founded by families of affected children in order to raise funds for future research and treatment. This syndrome is based on the lack of a gene or part of a gene on chromosome 5. This rare Disorder causes a significant developmental delay, with autism spectrum traits and epileptic seizures.



There is now a research team, led by Dr. Stuart Lipton, who is developing possible treatments for this disease. Join us in supporting Dr. Lipton and his team of researchers.




Thank You! We Made Our Goal!
We sold 106 on a goal of 100.

Thank you to everyone for your support in helping us reach our fundraising goal! Our t-shirt is being produced!.

This fundraiser ended on March 23, 2019.





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