SNYDER-ROBINSON FOUNDATION

The Snyder-Robinson Foundation is a nonprofit organization with a mission to advance research relating to Snyder-Robinson Syndrome (SRS) & related disorders The Snyder-Robinson Foundation is a tax-exempt organization formed to advance medical and scientific The mission of The Snyder-Robinson Foundation is to find treatments or a cure for Snyder-Robinson Syndrome (SRS), and for related charitable, educational, and scientific purposes.

HASHIMOTOS ENCEPHALOPATHY SREAT ALLIANCE

𝙋𝙧𝙤𝙫𝙞𝙙𝙞𝙣𝙜 𝙥𝙖𝙩𝙞𝙚𝙣𝙩 𝙨𝙪𝙥𝙥𝙤𝙧𝙩 𝙩𝙤, 𝙥𝙪𝙗𝙡𝙞𝙘 𝙖𝙬𝙖𝙧𝙚𝙣𝙚𝙨𝙨 𝙤𝙛, & 𝙢𝙚𝙙𝙞𝙘𝙖𝙡 𝙧𝙚𝙨𝙚𝙖𝙧𝙘𝙝 𝙛𝙤𝙧 𝙃𝙀/𝙎𝙍𝙀𝘼𝙏 & 𝙎𝘼𝙀 Providing patient support to, public awareness of, and medical research for Hashimoto's Encephalopathy (HE)/SREAT and Seronegative Autoimmune Encephalitis (SAE).

• Private Grantmaking Foundations

• 435.

Brian J Kelley Foundation for Hope Inc

Through Brian’s Hope, a 501(c)(3) charitable foundation, we look forward to when no child experiences the devastation of adrenoleukodystrophy (ALD) Through Brian’s Hope, a 501(c)(3) charitable foundation, we look forward to a day when no child will experience the devastation of adrenoleukodystrophy (ALD).

• Public Foundations

• 436.

Metrodora Foundation

Catalyzing scientific collaboration and discovery to find cures for complex chronic disorders.

• Cancer Research

• 437.

Dianas Fibroid Foundation Inc

Dianas Fibroid Foundation DFF was established in honor of Diana Leigh Tomkinson who courageously battled a rare malignancy for nearly 4 years that may have been associated with her decades long struggles with uterine fibroids leiomyomas.

• Private Grantmaking Foundations

• 438.

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.

• Professional Societies & Associations

• 439.

Sturge-Weber Foundation

Embracing our uniqueness. We may be rare, but we're also one in a million.

• Birth Defects, Genetic Diseases Research

• 440.

International FOXP1 Foundation

Our mission is to build a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge, inspiring hope, supporting research, and raising awareness.

• Fund Raising and/or Fund Distribution

• 441.

Maxwell James Oskam Foundation Inc

To make a difference in the world in Maxwell's honor by blessing others, as we were blessed by Maxwell's life, to improve lives and raise awareness of Neuroblastoma, and raise funds that will directly be utilized to advance the progress of Neuroblastoma research.