• Fund Raising and/or Fund Distribution

• 451.

Lupus Research Institute Inc

The Lupus Research Alliance is the world’s largest private funder of lupus research.

• Alliance/Advocacy Organizations

• 452.

PSC Partners Seeking a Cure

The mission of PSC Partners Seeking a Cure is to drive research to identify treatments and a cure for primary sclerosing cholangitis (PSC), while providing education and support for those impacted by this rare disease.

• Birth Defects, Genetic Diseases Research

• 453.

Kate Foundation for Rett Syndrome Research Inc

The Kate Foundation is a 501(c)(3) organization dedicated to raising research funding for the reversal of Rett Syndrome and related disorders.

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

• 454.

National Niemann-Pick Disease Foundation

National Niemann-Pick Disease Foundation The NNPDF offers support and guidance to families and patients of those affected by Niemann-Pick Dise Mission: We are a non-profit group dedicated to supporting and empowering patients and families affected by Niemann-Pick disease through education, collaboration and research.

Connective Tissue Coalition, Inc

Empowering Progress; Inspiring Hope Our Mission: The Connective Tissue Coalition (CTC) drives research, raises awareness, and provides resources for individuals affected by Ehlers-Danlos, Marfan, and Loeys-Dietz Syndromes.

• Human Services - Multipurpose & Other N.E.C.

• 456.

Life and Limb Restoration Inc

Together we can Transform the quality of life for people with disabilities by improving access to prosthetics services in Cameroon Our Impact Weve worked on improving the lives of over 40 young people through direct practice.

• Specifically Named Diseases

• 457.

Abetalipoproteinemia and Related Disorders Foundation

Abetalipoproteinemia and Related Disorders Foundation is a non-profit, volunteer organization that provides guidance on needed scientific research, diagnosis, and management of abetalipoproteinemia and related hypolipidemias.

• Alliance/Advocacy Organizations

• 458.

Ipex Foundation

The IPEX Foundation’s purpose is to improve the treatment, quality of life and the long term outlook for children and adults living with IPEX syndrome through research, support, education and advocacy to families and patients.

Action for Aidan

Please Help Us to Raise Money for Hunter Syndrome research.