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The mission of Hospice of the Sacred Heart is to provide comfort, care, hope and choice to patients and their families while guiding them through their end of life journey.

Your support makes it possible for us to offer high-quality patient education from top scleroderma experts, facilitate patient support groups and fund promising research.

The mission of HLAA is to open the world of communication to people with hearing loss by providing information, education, support and advocacy. Founded in 1979, HLAA is the leading organization for people with hearing loss in the United States.

The Aplastic Anemia and Myelodysplasia Association of Canada is a federally incorporated and registered national charity with the goal of providing a seamless support network for every Canadian patient, family member, friend and concerned healthcare provider dealing with aplastic anemia, myelodysplasia (also known as myelodysplastic syndrome, or MDS) or PNH. Led by a volunteer board of directors and a distinguished team of medical advisors from across Canada, the association has a number of provincial chapters.

United Spinal Association works to empower and advocate for people with spinal cord injuries/disorders and all wheelchair users by providing peer support, information and resources, and by lobbying for accessibility and disability rights. Their programs include a national chapter network, resource/assistance services, advocacy, and publications to improve quality of life for people with SCI/D.

The Alberta Lymphedema Association (ALA) is a not for profit charitable organization founded in 2003 by a team of people who recognized the need to help people living with, or at risk of, lymphedema. A learning association committed to ongoing education of its stakeholders, ALA works to make a difference and empower affected individuals and their families to help manage this condition. ALA works from the patient standpoint.

Williams syndrome is a genetic disorder that affects approximately 30,000 people in the United States. The Williams Syndrome Association is the United States' go-to support network and strives to enrich the lives of individuals and families affected by Williams syndrome.

Founded in 1972, the Chinese Progressive Association educates, organizes and empowers the low income and working class immigrant Chinese community in San Francisco to build collective power with other oppressed communities to demand better living and working conditions and justice for all people.

The Kennedy's Disease Association's mission is to inform, support, educate, fund research and find a cure for Kennedy's Disease.

Located on the outskirts of Frelighsburg, Camp Garagona was founded in 1969. It is a camp for people living with a metal deficiency and/or an autism spectrum disorder, young and old alike. The Association is a charity, financed mainly by the registration fees of our campers, some government subsidies, and charitable donations by businesses, foundations, and individuals. It should be noted that most of our users are underprivileged financially.