• Private Grantmaking Foundations

• 37.

The Esther A and Joseph Klingenstein Fund Inc

Klingenstein Philanthropies is comprised of three foundations focused on neuroscience, children’s health, early literacy, and the environment.

• Epilepsy Research

• 38.

Bridge the Gap

SYNGAP1 Foundation is a legacy page dedicated to preserving the work and mission of our 100% charitable nonprofit in the USA, focused on #SYNGAP1 To serve, educate and fund research for families coping with the effects of SYNGAP mutations.

The NVLD Project

We are a non-profit organization that is raising awareness and building support for children, adolescents and adults with #NVLD.

• Diseases, Disorders, Medical Disciplines N.E.C.

• 40.

National Niemann-Pick Disease Foundation

National Niemann-Pick Disease Foundation The NNPDF offers support and guidance to families and patients of those affected by Niemann-Pick Dise Mission: We are a non-profit group dedicated to supporting and empowering patients and families affected by Niemann-Pick disease through education, collaboration and research.

• Community Health Systems

• 41.

Neuro Vitality Center

To improve the quality of life of individuals and their families living with stroke and related neurological conditions through community-centered care, support, education and research.

Pace Foundation

A national non-profit patient organization dedicated to improving diagnosis & treatment of persons with Pediatric Autoimmune Neurological Disorders The Pediatric Autoimmune neurologiCal rEsearch (PACE) Foundation, is a national non-profit patient organization dedicated to researching these disorders.

• Alliance/Advocacy Organizations

• 43.

Charlotte and Gwenyth Gray Foundation

Sisters, Charlotte & Gwenyth, were diagnosed w/ Batten Disease, a rare & fatal brain disease.

• Alliance/Advocacy Organizations

• 44.

Lissencephaly Foundation Inc

Empowering Families & Educating Communities by promoting a day of awareness, hosting family gatherings, providing family support, & educational material.

Texas Neurofibromatosis Foundation

We’re a community of NF patients, parents, doctors and advocates who want to listen, support or help you as we can.