• Alliance/Advocacy Organizations

• 235.

Colon Cancer Alliance for Research and Education for Lynch Syndrome

The non-profit dedicated to Lynch Syndrome education & awareness, the # 1 hereditary cause of uterine & colon cancers.

• Blood Supply Related

• 236.

Community Blood Center Inc

Connecting lives and sharing life – that’s what The Community Blood Center (CBC) has been doing since 1955.

MOWAT-WILSON SYNDROME FOUNDATION

This is the official page for the Mowat-Wilson Syndrome Foundation.

• Cancer

• 238.

GORLIN SYNDROME ALLIANCE

Empowering those with Gorlin Syndrome to live rich, full, happy lives.

• Nerve, Muscle, and Bone Research

• 239.

Lgmd2L Foundation

We’re a nonprofit searching for a cure for LGMD2L, a rare disease that causes muscle weakness and atrophy, pain, and eventually leads to many sufferers being unable to walk.

• Private Grantmaking Foundations

• 240.

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.

Rare New England Inc

Rare New England's Mission is to bring together New England patients and families touched by rare and complex disorders.

• Mutual/Membership Benefit Organizations, Other N.E.C

• 242.

SCA27b Ataxia Foundation

Gliding into the future to beat Ataxia Our mission is to improve the quality of life of individuals and families affected by SCA27b while promoting research and treatments for Ataxia.

• Alliance/Advocacy Organizations

• 243.

Progressive Familial Intrahepatic Cholestasis

PFIC advocacy and resource network Inc.