Scarring Alopecia Foundation

Cicatricial Alopecia Research Foundation (CARF) is the world's only voice for people with Cicatricial Alopecia Scarring Alopecia Foundation (SAF) is a nonprofit public charity organization and the world's only v The mission of the Scarring Alopecia Foundation (SAF) is to provide education and patient support, raise public awareness, and advance and promote research.

• Health Support Services

• 614.

Foundation for Prevention

Our Mission The Foundation for Prevention is a notforprofit 501c3 organization dedicated to promoting disease prevention methods that work.

American Neuromuscular Foundation

With your help, the American Neuromuscular Foundation (ANF) can fund research that will improve the lives of patients with neuromuscular diseases.

Leah Still Foundation, Inc.

Our mission is based on Leah’s family’s journey with childhood cancer.

Kcnq2 Cure Alliance Inc

Our promise is to educate and to advance research leading to treatments or a cure for patients living with the genetic disorder KCNQ2 Raising awareness, educating, and advancing research for KCNQ2 Developmental and Epileptic Encephalopathy.

• Private Grantmaking Foundations

• 618.

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).

• Private Grantmaking Foundations

• 619.

Alpha Foundation Inc

Alpha Foundation Inc. Your Custom Text Here Alpha Foundation Inc.

• Medical Specialty Research

• 620.

Global Society of Rare Genitourinary Tumors Inc

International Society dedicated to improving the care of rare GU tumors through cutting edge science and the promotion of education.

• Alliance/Advocacy Organizations

• 621.

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.