• Public Foundations

• 388.

The Sumaira Foundation

Raising global awareness of #NMOSD & #MOGAD, building community, supporting research, advocating for rare disease patients/caregivers.

Prader-Willi Syndrome Association | USA

What’s YOUR story. Tweet us and tell us what it’s like #GrowingUpRare We hope you will suggest the PWSA | USA facebook page to your friends.

• Birth Defects, Genetic Diseases

• 390.

Huntingtons Disease Socitey of America Group Return

The Huntington’s Disease Society of America is the premier nonprofit organization dedicated to improving the lives of everyone affected by Huntington’s disease.

BARROW NEUROLOGICAL FOUNDATION

Our mission is to be the catalyst of our donors’ passion for transformation by providing the resources for Barrow Neurological Institute to achieve its mission.

• Nerve, Muscle, and Bone Diseases

• 392.

The Lilly and Blair Foundation

The Lilly and Blair Foundation is dedicated to improving the lives of children battling de novo spastic paraplegia - a swift and severe neurodegenerative disease - through collaboration with top scientists and funding of promising research.

Rare New England Inc

Rare New England's Mission is to bring together New England patients and families touched by rare and complex disorders.

• Other Mental Health, Crisis Intervention N.E.C.

• 394.

Dmddorg

Explore DMDD. org Discover Valuable Resources Join Support Groups and Engage in Research Overcoming DMDD through shared support and resilience.

Sickle Cell Disease Association of America MI Chapter Inc

Education, genetic counseling, advocacy, follow-up laboratory testing, case management, events, medical referrals, summer camp, and more.

National Ataxia Foundation Incorporated

Our mission is to accelerate the development of treatments and a cure while working to improve the lives of those living with Ataxia.