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Seva Foundation works to prevent blindness and restore sight worldwide. Our programs build the capacity of underserved communities to provide comprehensive and high-quality eye care that is accessible by all.

The Orthopaedic Foundation for Active Lifestyles encourages general practitioners and other members of the professional allied health care community whose practices include the care of persons with sports-related musculoskeletal injuries to participate in educational courses and hands-on laboratory workshops concerning advances in orthopaedic surgery, physical medicine and rehabilitation.   The Foundation is dedicated to the development and presentation of unique continuing medical education and research programs for physicians, health care professionals and interested community groups. Its focus is:

The Nightscout Foundation exists to encourage and support the creation of open source technology projects that enhance the lives of people with Type 1 Diabetes and those who love them. This includes fundraising, advocacy, and direct software and hardware development.

The Bow Foundation is dedicated to supporting GNAO1 families through enhanced research and increased awareness. We're working to fund cutting edge research to benefit those with GNAO1 disabilities and other similar rare diseases and neurological conditions.

Take Action Today, Breathe Better Tomorrow The COPD Foundation is a patient-centered organization committed to preventing COPD, bronchiectasis, and nontuberculous mycobacterial (NTM) lung disease, and to seeking cures while improving lives and advocating for all affected.

The mission of the Life Foundation is to stop the spread of HIV and AIDS in Hawaii, to empower those affected by HIV/AIDS to maximize the quality of their lives, to provide leadership and advocacy and to apply lessons learned in the AIDS epidemic to other related areas of public health or concern.

Our mission is to raise money for children whose families cannot afford the necessary medication or treatment for Lyme disease. We provide grants and support the medical community until a cure is found. LivLyme Foundation will promote education and awareness about Lyme and the associated diseases.

The MAGIC Foundation was established by five families October 29, 1989. After countless frustrating searches for solid information regarding their own child's growth disorder, these parents decided to join together and form an organization that would make this search easier for other parents. MAGIC's primary function is to provide families and children with services to help them better understand their diagnosis, and to give them the support needed to cope with the realities of these greatly misunderstood disorders.The mission of The MAGIC Foundation is to identify and expand treatment of physical abnormalities in children resulting from growth disorders. To remain the non-profit leader committed to excellence in developing and sustaining innovative educational, outreach and support programs.

Our mission at Jett Foundation is to extend and enrich the lives of individuals affected by Duchenne muscular dystrophy and other neuromuscular disorders. We fulfill this mission by partnering with individuals and families through empowering educational programming, transformational direct service experiences, and by accelerating development of life-changing treatments.

SARAH is a family of agencies, SARAH Inc., SARAH SENECA, and SARAH Tuxis, that provide programs and services for people with intellectual and other disabilities who live in Connecticut. The SARAH Foundation, Inc. is responsible for raising funds, managing the investments and coordinating all donations in accordance with the wishes of the Donors and the mission of the SARAH agencies.

The LGS Foundation is a nonprofit organization dedicated to improving the lives of individuals impacted by LGS through advancing research, awareness, education, and family support. Our vision is to end the suffering and devastation caused by LGS. Lennox-Gastaut Syndrome (LGS) is a severe epilepsy syndrome that develops in young children and often leads to lifelong disability.

The Amalia Foundation was founded in honor of our mother as a way to honor her legacy and help those with Parkinson's Disease. Our mom touched many people during her life. She loved running and exercise, and since her death we have looked at different ways to honor her memory. To that purpose, we have founded The Amalia Foundation, with the goal of supporting exercise programs for those with Parkinson's. There are many excellent charities that support research and studies, but we wanted something that had the ability to positively influence people and caregivers in our own area and in their daily life. A wonderful program, Delay the Disease was started by David Zid and Jackie Russell in Columbus, Ohio. It has expanded all over the country and offers a simple exercise program that has the ability to help ease the daily struggles of Parkinson's, and delay some of the more devastating results of the disease through exercise. This program can give people some of their independence back and help them deal with the day to day issues of living with Parkinson's. The Amalia Foundation has already sponsored the licensed Delay the Disease training program in Cleveland, for physical therapists and other health care professionals. Beginning in April 2013, exercise classes begin at various locations in Northeast Ohio for those with Parkinson's and their caregivers. The goal is to continue to add classes and locations to serve our community. Our motto is taken from a quote by Mother Theresa: "We can do no great things, only small things with great love." Help us support people and their families as they deal with Parkinson's.