Welcome to our Rare Disease Resources hub, where you'll find a wealth of information and insights about organizations, institutions, and companies dedicated to making a difference in the world of rare diseases. In this section, we provide brief descriptions of each resource, summarizing their vital roles in research, advocacy, and support for individuals living with rare conditions. Whether you're seeking knowledge about groundbreaking research initiatives or innovative pharmaceutical advancements, this page is your gateway to discover the invaluable contributions of these remarkable entities. For more in-depth information, simply click on the organization or company of interest to learn about their mission, ongoing projects, and the impact they're making within the rare disease community.
National MPS Society
The National MPS Society provides support and advocacy for individuals and families affected by mucopolysaccharidoses (MPS) and related disorders.
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Alport Syndrome Foundation
The Alport Syndrome Foundation supports research and provides information and resources to those living with Alport syndrome, a rare genetic kidney disease.
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National Tay-Sachs & Allied Diseases Association (NTSAD)
NTSAD provides support, information, and advocacy for families affected by Tay-Sachs, Sandhoff, GM1, and Canavan diseases, which are rare genetic disorders.
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National Gaucher Foundation
National Gaucher foundation supports individuals and families affected by Gaucher disease, a rare genetic disorder that affects various organs and systems.
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Friedreich's Ataxia Research Alliance (FARA)
FARA is dedicated to advancing research and providing support for those affected by Friedreich's ataxia, a rare neurodegenerative disorder.
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