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The Huntington's Disease Society of America is the premier nonprofit organization dedicated to improving the lives of everyone affected by Huntington’s disease. From community services and education to advocacy and research, HDSA is the world’s leader in providing help for today and hope for tomorrow for people with Huntington’s disease and their families. HDSA's network of chapters, affiliates, HDSA Centers of Excellence, social workers and support groups provides a seamless connection for help, education and outreach to HD families and health care professionals across the United States.
The mission of Kansas City Hospice and Palliative Care is to bring expert care, peace of mind, comfort, guidance, and hope to people who are affected by life-limiting illness or by grief. And, our vision is each person in our community is valued from life through death and each family is supported in their grief. See also Kansas City Hospice Foundation.
Samaritan Hospice provides specialized medical care and emotional support for people facing serious and progressive illness in the comfort of their homes or other residences. Samaritan offers an interdisciplinary team of nurses, social workers, home health aides, spiritual support coordinators, bereavement counselors and volunteers to help patients and their families live as fully and comfortably as possible through individualized plans of symptom management and emotional support. Services are provided regardless of financial circumstances. Samaritan has been an innovative provider of hospice care since its inception in 1980. It is now one of the 15 largest providers of hospice care in the country. It has cared for more patients than any other hospice in the Middle Atlantic States and remains on the cutting edge of hospice care.
Rally Foundation, a 501(c)(3) non-profit organization, empowers volunteers across the country to raise awareness and funds for childhood cancer research to find better treatments with fewer long-term side effects and, ultimately, cures.
Founded in 1988 by Paul Newman, The Hole in the Wall Gang Camp is a community dedicated to providing “a different kind of healing” to children and their families coping with cancer, sickle cell anemia, and other serious illnesses. Through summer sessions and family weekends at the Camp in Ashford, Connecticut and year-round outreach to hospitals and clinics across the Northeast, the Camp serves more than 20,000 children and family members annually. All services are provided free of charge.
The core mission of the IRSF is to fund research for treatments and a cure for Rett syndrome while enhancing the overall quality of life for those living with Rett syndrome by providing information, programs, and services. In 1983, a small dedicated group of parents whose children had Rett syndrome formed the first non-profit to focus exclusively on Rett syndrome – International Rett Syndrome Association (IRSA). In 2007, IRSA and Rett Syndrome Research Foundation (RSRF) consolidated resources to better serve families and maximize research investments toward a cure. The International Rett Syndrome Foundation (IRSF) emerged with a mission to accelerate research and empower families that builds upon these foundations’ pioneering work toward care and cure. We are walking this journey with you. IRSF is comprised of parents and friends of those diagnosed with Rett syndrome. We are dedicated to empowering families with the latest medical information, offering meaningful support and resources, and advocating for all those living with Rett syndrome. Our strategy is simple but powerful: improve care today and create treatments for tomorrow. IRSF is committed to a full-spectrum approach, providing solutions for everyone living with Rett syndrome. We do this by investing in innovative research, working to build a robust treatment pipeline, and removing barriers to ensure clinical trial success.
The Ekal Foundation's mission is to combat illiteracy and provide primary education for every child in every village in india. Also, Ekal works towards the social and economic development of the entire village through healthcare, livelihoods and civic empowerment programs.
Our mission is to improve the experience, outcomes, and survival of teens and young adults with cancer by providing facilities and programs designed especially for them in hospitals throughout the USA.
NADAP’s mission is to enable individuals to become healthy, productive and self-sufficient.
Children's Cancer Research Fund is a national organization dedicated to curing childhood cancer by investing in the most effective research, collaborating with the most talented minds, inspiring and educating advocates worldwide to take action and supporting families.
Cedars-Sinai Health System, a non-profit, independent health care organization is committed to leadership and excellence in delivering quality healthcare services: - Expanding the horizons of medical knowledge through biomedical research - Educating and training physicians and other healthcare professionals - Striving to improve the health status of our community
Angela Hospice is dedicated to provide comprehensive, compassionate, and Christ-like care to adults and children in the communities we serve.