AMERICAN EPILEPSY SOCIETY

American Epilepsy Society We are a community of professionals engaged in the understanding diagnosis study prevention treatment and cure with the goal of improving outcomes for persons with epilepsy.

Community Behavioral Health Philadelphia

Managing the delivery of behavioral health services for Medicaid recipients in Philly for 25 years.

• Nerve, Muscle, and Bone Diseases

• 876.

Reflex Sympathetic Dystrophy Syndrome Association (RSDSA)

RSDSA's mission is to provide support, education, and hope to everyone affected by #CRPS / #RSD while we drive research to develop better treatment and a cure.

• Human Service Organizations

• 877.

Healthy Parkinson's Communities of the Greater Capital Region Inc

Help for Parkinson’s is a non-profit organization to help inspire and support our community.

• Private Grantmaking Foundations

• 878.

Wallace Beeson Foundation Inc

A 501(c) founded in 2017 to raise money for research in rare Neurogastrointestinal & Motility Disease Home About Research Our Team More JOIN OUR FIGHT TOMAKE RARE KNOWN Funding Research for Rare Neurogastrointestinal Motility disorders YOUR DONATION FUNDS A DESPERATE NEED IN RESEARCH HOW WE STARTED From being a healthy 15yearold competitive swimmer to having to fight for herlife almost overnight Wallacesaw first hand the effect a rare condition has on someone.

• Patient Services�Entertainment, Recreation

• 879.

Bridgiing Resources

Category Connecting Families with Resources they need We are committed to supporting individuals and families impacted by any neuromuscular diagnosis by helping them understand their new diagnosis and assisting with navigating medical and educational environments.

• Specifically Named Diseases

• 880.

Sisters Hope Foundation for Hereditary Diffuse Leukoencephalop

We are dedicated to amplifying patient voices, and one day meeting the first survivor of ALSP.

AMERICAN SLEEP APNEA ASSOCIATION INC

American Sleep Apnea Association. Patient-Led & Patient-Supported Nonprofit.

• Birth Defects, Genetic Diseases Research

• 882.

THE NATIONAL FRAGILE X FOUNDATION

News and information from the National Fragile X Foundation about Fragile X syndrome, FXTAS, FXPOI and the other Fragile X-associated disorders Since 1984, the National Fragile X Foundation has been providing knowledge, resources and tools to families living with Fragile X and the professionals support them throughout their lifespan.