• Alliance/Advocacy Organizations

• 829.

Wilson Disease Association

Wilson disease is a genetic disorder of having excessive copper accumulation in the liver or brain that is fatal unless detected and treated Welcome to the official fan page of The Wilson Disease Association International.

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

• 830.

The Neuromodulation Foundation, Incorporated

To contribute to the improvement of the health and well-being of patients suffering from various debilitating neurological and medical conditions by providing education about the medical therapy known as neuromodulation and by reporting the results of scientific research in the field of neuromodulation.

Scheuermanns Disease Fund

Scheuermann's Disease Fund - Raising Global Awareness for this Spinal Deformity The Scheuermann’s Disease Fund was created to improve the public's awareness and recognition of this spinal deformity, work towards improving early detection in adolescents, and to work with the medical community to better understand the long-term secondary effects Scheuermann's can cause.

• Cancer

• 832.

Baileys Foundation

Stella January 23 2017 February 22 2023 Medulloblastoma Baileys Foundation is a federal 501c3 nonprofit founded in 2014 after our precious Bailey lost her battle with neuroblastoma.

• Pediatrics

• 833.

Evan's Victory Against Neuroblastoma Foundation Inc

Support neuroblastoma research, bring joy to kids in treatment @ hospitals & clinics w/ Treats & Treasures Carts Progr.

• Alliance/Advocacy Organizations

• 834.

Maternal Alloimmunization Foundation

Our mission is to provide advocacy and support to those affected by maternal alloimmunization and its comorbid condition, hemolytic disease of the fetus and newborn.

MELANOMA RESEARCH FOUNDATION

The Melanoma Research Foundation (MRF) is the largest independent organization devoted to #melanoma.

• Alliance/Advocacy Organizations

• 836.

Loeys-Dietz Syndrome Foundation

The LDSF is a 501(c)3 non-profit organization organization dedicated to:--encouraging education about Loeys-Dietz syndrome and related connective tissue disorders to medical professionals and lay communities in order to aid in identification, diagnosis and treatment of Loeys-Dietz syndrome--fostering research about Loeys-Dietz syndrome--providing a support network, for individuals, parents and families affected by Loeys-Dietz syndrome This March were celebrating 20 years since LoeysDietz Syndrome was first identified.

• Brain Disorders

• 837.

Vein of Galen Malformation Support Network Inc

Providing VOGM families access to specialist through info, emotional, logistical & financial support Providing up to date information, resources, emotional and financial help to VOGM families.