• Birth Defects, Genetic Diseases Research

• 136.

The Evanosky Foundation

The Evanosky Foundation exists for the purpose of generating funds to support two main objectives.

• Specifically Named Diseases Research

• 137.

A Foundation Building Strength Inc

Our mission is to find treatments for Nemaline Myopathy.

• Fund Raising and/or Fund Distribution

• 138.

Familial Dysautonomia (FD) Foundation, Inc.

FD Foundation is the leader in FD treatment and research.

• Private Operating Foundations

• 139.

DEATER FOUNDATION INC

Deater Foundation Inc. works to provide funding and support for medical research on HSAN1, a hereditary sensory neuropathy, with the goal of advancing understanding, awareness and helping to bring about a potential treatment/cure for this disease.

• Birth Defects, Genetic Diseases

• 140.

International Rett Syndrome Association, Inc.

We are transforming lives every day in our fight to treat and cure Rett syndrome and better the lives of families living with this devastating disorder.

• Fund Raising and/or Fund Distribution

• 141.

Better Future 4 U

501(c)(3) nonprofit who’s mission is to fund research that leads to a treatment for individuals with HNRNPU A nonprofit organization looking to create a better future for those affected by HNRNPU and where a treatment for this rare genetic disorder is found.

• Nonmonetary Support N.E.C.*

• 142.

Kitalys Institute Inc

Home About Us Events Press Support Us Contact More Preserve Health Protect Against Disease Prolong Healthspan Meeting the Great Challenge of Increased Healthspan for AllTake the Moonshot to accelerate and promote the translation of scientific advances into material accessible and sustainable gains in public health.

International Rett Syndrome Foundation

We are transforming lives every day in our fight to treat and cure Rett syndrome and better the lives of families living with this devastating disorder.

MUSCULAR DYSTROPHY FAMILY

The Muscular Dystrophy Family Foundation uses the power of giving to increase the quality of life and independence of people with muscular dystrophy—and empower their families—through advocacy, education, and financial assistance Living with a neuromuscular disease means facing new challenges every day.