The Fibromuscular Dysplasia Society of America (FMDSA) is a not-for-profit patient advocacy organization dedicated to improving the diagnosis and treatment of Fibromuscular Dysplasia (FMD). They work towards this goal by raising awareness of FMD, funding research activities, providing support to patients and their families, and educating both patients and the healthcare community.
With a focus on awareness, education, and research since 2003, FMDSA has made significant strides in understanding FMD and its treatment. They have established a research network and patient registry to identify patient characteristics associated with FMD and explore potential markers of the disease. Through their efforts, FMDSA has become a recognized authority on FMD, providing valuable resources and support to patients and healthcare professionals alike.
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