
Rett Syndrome Research Trust UK was formed as a grassroots effort by parents of daughters with Rett Syndrome who want to impact the speed at which treatment can be developed for girls and women living with Rett Syndrome today.
The Board of Trustees of RSRT UK comprises of 100% parents of daughters with Rett Syndrome:
Working with the Rett Syndrome Research Trust, our shared name and synchronized efforts reflect our common goal; to accelerate treatment for Rett Syndrome and related MECP2 Disorders.