• Museums & Museum Activities

• 145.

Prader Willi Association of New England Inc

PWS is a non-inherited genetic disorder which is associated with a random deletion of the 15th chromosome.

• Christian

• 146.

Embracing Life Through Love LLC

To encourage and support care for individuals with ALS and other diseases and illnesses; to assist and support any and all clinical treatment education, and promotion of independence; to engage in fundraising activities and solicit gifts and donations for the purpose of the Corporation.

• Fund Raising and/or Fund Distribution

• 147.

The Terri@Levine Foundation for Children With Rsd

We support children and families throughout North America in need of money for treatment not covered by insurance.

• Birth Defects, Genetic Diseases

• 148.

Tennessee Prader-Willi Association, Inc.

We provide support and information for people with PWS & their families.

HOPE IN FOCUS INC

Transforming the lives of those affected by blindness from inherited retinal disease.

• Private Grantmaking Foundations

• 150.

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.

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

• 151.

The Reid Foundation for Lupus

The Reid Foundation for Lupus is a 501(c)(3) dedicated to raising awareness, promoting research, and advocating for people living with lupus.

• Fund Raising and/or Fund Distribution

• 152.

Gillette Children's Hospital Foundation

We are a global beacon of care for patients with brain, bone and movement conditions.

• Fund Raising and/or Fund Distribution

• 153.

THE CHAMP FOUNDATION

Mission The Champ Foundation supports research toward better treatment and a cure for single largescale mitochondrial deletion syndromes SLSMDS like Pearson syndrome.