• Research Institutes and/or Public Policy Analysis

• 64.

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.

• Fund Raising and/or Fund Distribution

• 65.

COALITION TO CURE CHD2 INC

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

Young Adults With Epilepsy Central Coast Inc

Educate, Empower & Support Young Adults with Epilepsy (YAWE) At Young Adults with Epilepsy (YAWE), our mission is to foster resilience and independence in young adults with epilepsy from the Central Coast.

Epilepsy Leadership Foundation Inc

The Epilepsy Leadership Foundation (ELF) is a 501 (c) 3 nonprofit organization dedicated to empowering young people living with epilepsy and their families💜 Epilepsy Leadership Foundation (ELF) is a 501 (c) 3 nonprofit empoweing people with epilepsy The Epilepsy Leadership Foundation (ELF) is dedicated to empowering children with epilepsy/seizures to reach their full potential.

Revolutionize Dmdd

Revolutionize DMDD is to help transform the lives of children and adolescents suffering from Disruptive Mood Dysregulation Disorder (DMDD).

• Specifically Named Diseases Research

• 69.

SLC6A1 CONNECT

People Magazine Exclusive Milestones for Maxwell What if your child was diagnosed with a disease so rare it didnt have a name.

Citizens United for Research in Epilepsy

CURE Epilepsy is the leading nongovernmental funder of epilepsy research, with over 300 grants funded in 18 countries to date.

THE EPILEPSY FOUNDATION OF NORTHWESTERN

Mission of the Epilepsy Center of Northwest Ohio is to improve the lives of people affected by epilepsy and those with developmental disabilities The Mission of the Epilepsy Center of Northwest Ohio is to improve the lives of people affected by epilepsy and those with developmental disabilities.

• Birth Defects, Genetic Diseases

• 72.

CACNA1A Foundation

Nonprofit dedicated to a brighter future for those with CACNA1A variants.