Decoding Developmental Epilepsies

We serve two distinct communities. First, we serve those living with SCN8A and their families.

• Fund Raising and/or Fund Distribution

• 2.

COALITION TO CURE CHD2 INC

Fighting for our kiddos, and others, with CHD2-related neurodevelopmental disorders.

• Fund Raising and/or Fund Distribution

• 3.

Eleanor Kaplan Foundation Inc

To raise funds and awareness to develop cures for Ultra Rare Neurodegenerative Diseases.

• Neurology, Neuroscience

• 4.

Inadcure Foundation Inc

The INADcure Foundation is a 501c3 nonprofit charity whose mission is to support the development of treatments, including a cure, for Infantile Neuroaxonal Dystrophy (INAD) and other forms of PLA2G6-related neurodegeneration (PLAN).

• Birth Defects, Genetic Diseases

• 5.

Irf2Bpl Foundation

Raising Awareness and Research Funds for IRF2BPLDisorder This website provides the information onIRF2BPLrelated disorders for patients family members physicians and biomedical scientists working all together to solve the medical mystery on IRF2BPL.

• Specifically Named Diseases

• 6.

YBRP Inc

YBRP is a non-profit organization whose mission is to positively impact the lives of individuals with HNRNPH2 genetic variations.

• Alliance/Advocacy Organizations

• 7.

Finding Nori Foundation

The Finding Nori Foundation Home About Meet the Team Finding Joy Blog Resources Publications DONATE Contact Upcoming Events More Raising research funding for PAX5 and ALG13 related neurological disordersEmpowering families with ultra rare undiagnosed diseases to find answers Our Mission Our mission is to advance scientific research through fundraising and advocacy for ultra rare undiagnosed genetic disorders.

• Fund Raising and/or Fund Distribution

• 8.

Tough Genes Inc

Currently, there is no treatment for IRF2BPL-Related Disorder.

• Birth Defects, Genetic Diseases

• 9.

STXBP1 FOUNDATION

Non-profit dedicated to ending STXBP1-related disorders, rare neurodevelopmental and epileptic encephalopathies, and spreading awareness of this rare disease.