Our goals

Our association, created in May 2000, aims to be the spokesperson for families affected by Hirschsprung's disease.

By creating links with other rare disease associations,

by maintaining close relationships with the medical teams who treat this disease,

by disseminating reliable information,

and above all by offering our listening and our experience to families who need it!

To contact us

Send us an email: afmah.info@gmail.com

You can also find us on Facebook!