A place for families.
A path to a cure.
At the MEF2C Family Foundation, we are a community of families, advocates, and professionals united by a shared journey with MEF2C-related disorders — also referred to as MEF2C Haploinsufficiency Syndrome. We are here to connect, support, and empower families like yours.
Together, we partner with researchers and clinicians to deepen understanding, advance treatments, and work fiercely toward our ultimate goal: a cure.
Explore more
Find out more about this ultra-rare genetic condition.
Learn more about our children and their journey with this life-changing syndrome.
Be the first to learn about upcoming research opportunities and community news.
Who
we are
Our group is composed of the parents, friends, advocates and loved ones of people with MEF2C-related disorders. We’re motivated to support families affected by this condition, and work towards finding therapies and treatments for this rare genetic disorder.
Contact us
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