Organised by MECP2 Duplication FoundationMECP2 Duplication Syndrome is a rare neurological disease. As a result of recent research breakthroughs, it has the potential to be reversed. With your support, thousands of affected children and adults may one day receive a successful treatment.
The MECP2 Duplication Foundation is a family founded organization providing support for the MECP2 Duplication community. Our goal is to provide families diagnosed with this disorder information and support, to increase awareness of the disorder, and to provide funding to cutting edge research that will one day treat those affected and enhance their quality of life.
Charities pay a small fee for our service. Learn more about fees