• Specifically Named Diseases

• 586.

APS Foundation of America, Inc.

APS Foundation of America (#APSFA) is the only US org spreading #Antiphospholipid Syndrome #APS & #Lupus #Awareness.

• Down's Syndrome

• 587.

Down Syndrome Education USA

DSE transforms the lives of young people with Down syndrome through better education.

• Birth Defects, Genetic Diseases Research

• 588.

Down Syndrome Association of Minnesota

The Down Syndrome Association of Minnesota (DSAMn) is a nonprofit that serves individuals with Down syndrome and their families/caregivers.

• Digestive Diseases, Disorders

• 589.

Texas Society for Gastrointestinalendoscopy

One united voice for #gastroenterology in Texas.

• Specifically Named Diseases

• 590.

CURE ADSSL1

501(c)(3) non-profit patient advocacy group with the mission to find treatment for ADSSL1 myopathy Mission of the CURE ADSSL1 organization is to invest in research and develop treatment options for patients with rare neuromuscular disease caused by mutation in ADSSL1 gene.

• Fund Raising and/or Fund Distribution

• 591.

Adelia Dundas Foundation Inc

Who We Are Support Us Events News Contact Apply More Lighting the Way for All Our MISSION The Adelia Dundas Foundation is a 501c3 non profit founded in 2023.

• Professional Societies & Associations

• 592.

Healthspan Action Coalition Inc

The mission is to advance biomedical research related to aging, longevity and healthspan.

• Alliance/Advocacy Organizations

• 593.

Voices of Friedreichs Ataxia Inc

Creating awareness about Friedreichs Ataxia Voices of Friedreich039s Ataxia FA We Have the Power to Overcome Anything Together.

Lambert-Eaton Lems Family Association

We advocate for patients, family and caregivers who have the extremely rare neuromuscular disorder, Lambert-Eaton Myasthenic Syndrome.