For the amazing group of ppl that started MEF2C Family Foundation (esp my wife :)), and all our kids.

The MEF2C Family Foundation is a group of parents who want to make a difference. 

Connection

**We connect, support, and empower families who have loved ones with MEF2C-related disorders.** We are a cooperative and welcoming group of parents that offers peer-to-peer support. By joining our community, we hope families will feel empowered to advocate for their loved ones and prepare themselves for the unique parenting journey that comes with raising a MEF2C child.

Research

**We are also advocates for curing this rare disease, and aim to connect clinicians, researchers, and biotech companies with our patient population.** We are committed to furthering research and treatments that will have a meaningful impact on our children’s quality of life. We believe we are stronger together, and we are hopeful that we will eventually treat or cure this rare disease.

MEF2C Family Foundation

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We are a nonprofit, so we rely on the generosity of donors like you.

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