Foundation for Angelman Syndrome Therapeutics

FAST is the premier patient advocacy organization working to cure Angelman syndrome.

• Research Institutes and/or Public Policy Analysis

• 2.

Riaan Research Initiative Inc

501(c)(3) non-profit organization hunting for a cure for rare and life-limiting genetic diseases that hurt children, starting with Cockayne syndrome.

• Birth Defects, Genetic Diseases Research

• 3.

Rare Olive Org Inc

Our mission is to push forward the scientific understanding and treatment options for a rare neurodevelopmental disorder.

• International Peace and Security

• 4.

Moonshotplatforminc

Rethink what's possible 🌕 #MoonshotPlatform is a digital movement connecting impact hackers with the key change-makers in pursuit of solving the 21st Century’s Grand Challenges.

Dlg4 Research Fund

DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation A page for people interested in learning more about DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation Mission To find specific treatment options and a cure for DLG4 patients by building a collaborative network of patients, families, clinicians and scientists that will work together to raise awareness and accelerate the understanding, diagnosis and treatment of DLG4 related synaptopathy.

CMT Research Foundation Inc

The CMT Research Foundation has one mission: Deliver treatments and cures for #CMT.

• Philanthropy/Charity/ Voluntarism Promotion (General)

• 7.

HOPEFUL HALOS FOUNDATION

About Share Event Info Register Contact More.

• Fund Raising and/or Fund Distribution

• 8.

PSFC

PSFC is a community of philanthropists dedicated to supporting psychedelic medicine and science.

• Fund Raising and/or Fund Distribution

• 9.

BENEFIT OTHERS FOUNDATION

Helping to overcome hardships and providing opportunities for children and their families Who We Are Benefit Others Foundation is a nonprofit 501c3 organization committed to enriching the lives of others.