Search Nonprofits

Black CAP is an organization that works to reduce HIV/AIDS in Toronto’s Black, African and Caribbean communities and enhance the quality of life of Black people living with or affected by HIV/AIDS. HIV/AIDS is spreading quickly in Toronto’s Black communities and we believe that our work is more important than ever. At this time, Black, African and Caribbean people account for more than one-fifth of all new HIV infections in Toronto, in the early nineties we made up only one-tenth of new HIV infections. Issues of HIV related stigma and discrimination, homophobia, anti-Black racism, immigration, poverty, and barriers to social inclusion also continue to make our work harder.

The Canadian Lyme Disease Foundation is a pro-active organization dedicated to advancing the research, knowledge, prevention, diagnosis, treatment, and control of Lyme disease (commonly misspelled as lymes disease, lyme's disease, lime disease, limes disease) and other tick-borne infections. The non profit Foundation plays a key role in providing reliable and accurate information to the public, medical community and government agencies about lyme disese lime disease and other tick-borne diseases and their potentially serious effects on our health and quality of life. The Canadian Lyme Disease Foundation works with patients, physicians and researchers throughout the world to obtain and provide scientific, peer-reviewed information on Lyme disease and other tick-borne infections such as Babesiosis, Erhlichiosis.

Our mission as the central voice in Michigan is to help prevent Lyme Disease and other Tick-Borne Disorders while providing support and education to Lyme Disease patients, caregivers, Health Care Professionals and the general public.

"Our goal is to provide up-to-date and credible information, dispel myths and misconceptions, and serve as a resource for anyone with questions about Lyme disease and other tick-related illnesses."

ADRC provides free support, education, and life‑enrichment programs for people with Alzheimer’s disease and other dementias and for their caregivers across Long Island. The organization focuses on care consultations, support groups, community education, and therapeutic programs (art, music, equine therapy, memory cafés) to help families manage cognitive decline and improve quality of life.

The mission of The Heart2Heart Foundation is to inspire and enable women and their loved ones to take action that prevents heart attack, stroke and premature death.

HeartGift provides life-saving congenital heart defect surgery to children from around the world where specialized medical treatment is either scarce or nonexistent.

Golden Heart Ranch (GHR) provides young adults with intellectual and development disabilities opportunities to reach their fullest potentials and enjoy meaningful, satisfying and joyful lives. We are an inclusive community where all young adults learn, work and create lifelong friendships in a supportive and caring environment.

Established in 1985, The ALS Association is dedicated to leading the fight to treat and cure ALS through global research and nationwide advocacy while also empowering people with Lou Gehrig's Disease and their families to live fuller lives by providing them with compassionate care and support. The Association builds hope and enhances the quality of life while aggressively searching for new treatments and a cure, through global research, providing assistance for people with ALS through a nationwide network of chapters, coordinating multidisciplinary care through certified clinical care centers, and fostering government partnerships.