The MEF2C Foundation was formed by a group of parents and relatives whose children are affected by MEF2C Haploinsufficiency Syndrome, with the goal of furthering research into MEF2C gene, associated conditions and the development of MEF2C targeted treatments for the collective benefit of all affected.

We are in close contact with a number of different researchers who are exploring therapies and treatments that could have a very real impact on the quality-of-life of sufferers and their families. We are also a hub of information for families impacted by MEF2C associated conditions and for those based in the UK are able to offer additional support with therapy and equipment needs.