Fibromuscular Dysplasia Society of America

Global Genes Global Advocacy Alliance member focused on rare disease support, education, advocacy, or research. The Fibromuscular Dysplasia Society of America (FMDSA) is a not-for-profit patient advocacy organization working towards better diagnosis and treatment of Fibromuscular Dysplasia (FMD). We do this by building awareness of FMD, funding research activities, providing support and educating patients and the health care community. FMDSA works to inspire and facilitate collaboration between national and international organizations devoted to FMD and FMD-related research, education, and patient care. Directory information only; not medical advice, legal advice, or endorsement. Services and eligibility should be confirmed with the organization.