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Hospice Support Foundation is a 501(c)(3) non-profit organization whose purpose is to honor the memory of hospice patients by providing assistance to those who are coping with life-limiting illness, death and grief. Donations to Hospice Support Foundation help support a wide variety of community-based services, research and education that can assist patients and families. To make a donation, please visit our website at www.hospicesupportfoundation.org.
The Arbor Hospice Foundation was founded in 2002 to provide philanthropic support and to advance the mission of Arbor Hospice in meeting the growing end-of-life care needs of the communities it serves.
HeartGift provides life-saving congenital heart defect surgery to children from around the world where specialized medical treatment is either scarce or nonexistent.
Joshua Frase Foundation (JFF) has worked tirelessly to increase awareness for Myotubular Myopathy and other neuromuscular disorders. JFF funds cutting edge genetic research for Myotubular Myopathy (MTM) at Children's Hospital Boston, Harvard & Wake Forest Medical School of Regenerative Medicine. JFF has built a network for families and friends affected by these devastating muscle disorders, giving them hope as the foundation pushes this research forward.
Halo House Foundation helps to save the lives of blood cancer patients by providing affordable and fully furnished housing so they can receive treatment at the Texas Medical Center.
Ellie’s Army Foundation provides financial assistance, support, and hope to children and young adults battling life-threatening illnesses in an effort to give them the best chance to survive.
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.
Our mission, "So the World May Hear," is about bringing understanding between people through caring and sharing. We believe caring develops trust and by sharing we find out humanity. We believe by growing engagement in this cause that we can increase tolerance and respect for life. Our goal is to pursue our mission with commitment so that future generations can live in a world with more caring and peace.
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.
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.