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Hope Clinic for Women provides confidential, faith-informed pregnancy support, women’s healthcare (including STI testing and well-woman care), counseling, and education to people facing unplanned pregnancy or pregnancy loss. The clinic focuses on medical services, emotional support, prevention/relationship education, and material referrals to help clients make informed choices and access community resources.

to improve the quality of life of those affected by sickle cell disease by promoting advocacy, education, research and excellent healthcare delivery.

NORD represents 1 in 10 Americans who have rare diseases with programs of advocacy, education, research and patients services. It serves as the voice of the rare disease community on important issues of public policy. It also provides information on rare diseases in understandable language for patients and their families, with referrals to support groups and other helpful resources. It encourages research on new diagnostics and treatments and administers patients assistance programs. NORD mentors rare disease support groups so that they can more effectively help their members. It serves as the point of connection between the patient community and key government agencies, such as the National Institutes of Health (NIH) and Food and Drug Administration (FDA). Nearly 150 patient organizations are members of NORD and look to NORD for guidance, mentoring and leadership.

The Heart and Stroke Foundation of Canada is a national voluntary non-profit organization whose mission is to improve the health of Canadians by preventing and reducing disability and death from heart disease and stroke through research, health promotion and advocacy. The Heart and Stroke Foundation of Canada is a federation of 10 provincial Foundations, led and supported by a force of more than 130,000 volunteers. For information on heart disease, stroke and healthy living, call 1-888-HSF-INFO (473-4636) or visit www.heartandstroke.ca

In 1973 as a result of the need for profound changes in mental health services the Alliance was incorporated in Los Angeles as the Coalition of Spanish Speaking Mental Health Organizations (COSSMHO). Since then the organization has grown and expanded to reflect the changing needs of the people and communities served. Today, the National Alliance for Hispanic Health is the premier science-based and community-driven organization that focuses on the best health for all. Community-based members provide services to more than 15 million Hispanics throughout the U.S. every year and national organization members provide services to more than 100 million people annually.

Also known as Kevin J Lederer Life Foundation: To promote health and alleviate the mental and physical distress of individuals and couples diagnosed with infertility through education and financial assistance.

To save young lives by advancing the knowledge and prevention of depression and suicide. Greater St. Louis, Missouri metropolitan area.

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.

Founded in 1957, the Sickle Cell Disease Foundation of California is the first and oldest, non-profit, social service sickle cell disease agency in the U.S. The MISSION of the SCDFC is to provide life- enhancing programs and services to individuals with sickle cell disease, to broaden public aware- ness about sickle cell disease and to promote medical research to find a cure. Currently approximately 250 million people worldwide carry the gene responsible for sickle cell disease (SCD) and other hemoglobin diseases. Each year about 300,000 infants are born with a major hemoglobin disease worldwide. In the US, 10% of the population is at risk for SCD. It is estimated that there are approx. 5,000 persons with sickle cell disease in Los Angeles.

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.