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GRIN2B Foundation is a parent-run organization dedicated to furthering research on the GRIN2B gene and providing support and education to the small, but growing community of individuals and families impacted by a GRIN2B diagnosis.

The NEHI Research Foundation aims to improve the lives of our patients and their families. As a foundation, we will support scientific research aimed at improving the diagnostic process, treatments, and ultimately finding a cure. We will work to facilitate dialogue among the medical and scientific community to expedite the discovery process and improve the care of patients. We will also work diligently to raise awareness. Last, but not least, we will provide financial assistance to patients and families as needs arise.

The foundation builds a global community to support families and individuals affected by FOXP1 syndrome, provides resources and education, and funds and promotes research to better understand the condition and advance potential treatments.

The Nepal Youth Foundation (NYF) transforms the lives of impoverished Nepali children by providing them with what should be every child's birthright – education, housing, medical care, and loving support.

Compassionate Eye Foundation (CEF) is an innovative, volunteer-driven, non-profit organization. CEF was founded on the principle that creative people as a community can and want to make a positive difference in the world.

The mission of the Ladybug CDH Foundation is to raise awareness of the birth defect congenital diaphragmatic hernia and to raise money to donate towards research and as financial assistance to families in the Pacific Northwest affected by CDH.

The TKO Strong Foundation is a non-profit organization dedicated to enhancing the lives of children born with Microvillus Inclusion Disease, by raising awareness and supporting research to find more effective treatment options.

The International FoxG1 Foundation’s Mission is to raise awareness and educate others about this rare genetic condition, to facilitate relationships within the FOXG1 community, and to raise funds to directly benefit families impacted by FOXG1.

The Propionic Acidemia Foundation is a 501(c)3 non-profit organization dedicated to finding improved treatments and a cure for Propionic Acidemia by funding research and providing information and support to families and medical professionals.

Your support allows recipient organizations to allocate resources directly to their needs and priorities. With strong foundations in their communities, whether it be in Quebec or in Africa, these organizations have demonstrated responsible financial management and democratic practices.

The mission of MPN Research Foundation is to stimulate original research in pursuit of new treatments — and eventually a cure — for the blood cancers essential thrombocythemia, polycythemia vera, and myelofibrosis, known collectively as myeloproliferative neoplasms (MPN).

The Evanosky Foundation exists for the purpose of generating funds to support two main objectives. It will support pediatric leukodystrophy research as well as assist and care for children and families affected by one of the leukodystrophies and/or other disabling conditions.