At the MVA Society, we know that families facing Mosaic Variegated Aneuploidy need more than research. They need information, guidance, and community.

Because MVA is one of the rarest conditions in the world, support services are still limited - but this is only the beginning. We’re building a hub of resources for families and professionals, and we want you to be part of shaping what comes next.

Every leaflet we create, every fact sheet we publish, and every piece of guidance we share is a step toward giving families answers and clinicians clarity. With your help, we can expand these resources and grow a support network that’s as pioneering as our research.