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 Ataxia Foundation
National Ataxia Foundation provides support, information, and advocacy for individuals and families affected by ataxia, a group of rare neurological disorders that affect coordination and balance.
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The National Urea Cycle Disorders Foundation
This foundation supports individuals and families affected by urea cycle disorders, a group of rare genetic metabolic disorders.
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EURORDIS
NNPDF is dedicated to supporting individuals and families affected by Niemann-Pick disease, a group of rare genetic disorders that affect lipid metabolism.
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Hope for HIE (Hypoxic Ischemic Encephalopathy)
Hope for HIE provides information, resources, and support for families affected by HIE, a rare brain injury that occurs during or shortly after birth.
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Multiple System Atrophy Coalition
Multiple System Atrophy Coalition supports individuals and families affected by multiple system atrophy (MSA), a rare neurodegenerative disorder.
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