Your membership brings us another step closer to achieving our goal of ultimately curing MPS and ML. Together we work to provide support and information to families affected with MPS; to increase public and professional awareness of MPS; and most importantly – to further the vital research that adds quality to all our lives.
Have you or a family member recently been diagnosed with MPS or ML? Visit our New Diagnosis webpage for additional information on beginning your journey with MPS or ML.
Membership Form for families/friends, professionals and corporate memberships who wish to register for membership by mail.