• Alliance/Advocacy Organizations

• 766.

CONGENITAL HYPERINSULINISM INTERNATIONAL

Improving the lives of babies, children, and adults with hyperinsulinism (HI) by supporting HI families, research, and awareness to prevent brain damage & death CHI is dedicated to improving the lives of people living with Congenital Hyperinsulinism.

Camp Hope Foundation

Camp Hope's mission is to serve kids and families affected by cancer, blood diseases and other catastrophic illnesses with free, in-person and medically safe camps and other support programs that build friendships, community and confidence.

• Heart and Circulatory System

• 768.

Trey Has Heart Foundation

To promote awareness and educate the public about Coarctation of the aorta, and the importance of early detection in children by speaking to students and families at local area school assemblies, youth sporting events and community health fairs, and the physical, emotional and financial toll this disease can have on affected children and their families.

Rare Trait Hope Fund

Rare trait Hope Fund facilitates research and provides funding for the development of treatments for a rare disease called Aspartylglucosaminuria (AGU) in hopes to save lives of AGU kids and adults.

• Fund Raising and/or Fund Distribution

• 770.

Harmony 4 Hope

Leading Nonprofit Mobilizing Community & Raising Funds 4 Rare Disease through the Universal Power of Music & Storytelling.

• Birth Defects, Genetic Diseases Research

• 771.

Valerias Foundation for Kcnt1 Research Inc

#rettevaleria #savevaleria #helpvaleria #supportvaleria #valeriasKCNT1 #raredisease #epilepsy #geneticdisorder #meinestimmefuereinleben #teamvaleria The Valeria Foundation is committed to achieving that: [+] to promote knowledge about the existence and cure of orphan diseases.

• Public Foundations

• 772.

Catalytic Impact Foundation Inc

Accelerating Breakthroughs by Funding Extraordinary Innovations and Visionary Leaders Addressing our Worlds Unmet Healthcare Needs The mission of the Catalytic Impact Foundation is to accelerate innovations in life sciences and healthcare funding companies that address unmet medical needs.

• Specifically Named Diseases Research

• 773.

ANN STEFFENS SCLERODERMA RESEARCH FOUNDATION INC

www. steffens-scleroderma. org Collaboration Drives Everything We Do The Steffens Scleroderma Foundation collaborates worldwide with researchers clinicians organizations and patients to improve the lives of those affected by rare diseases.

• Birth Defects, Genetic Diseases

• 774.

THINKGENETIC FOUNDATION INC

Helping those living with a genetic disease by shortening the time to diagnose a genetic condition and providing actionable, patient-focused guidance.