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The Pediatric Brain Tumor Foundation works to eliminate the challenges of childhood brain tumors. Our vision is a cure for childhood brain tumors.

Help a Life Foundation is a premier center of academic excellence for supporting and educating disadvantaged gifted girls to be agents of change in an emerging Ethiopian society.

The Brain and Behavior Research Foundation is committed to alleviating the suffering caused by mental illness by awarding grants that will lead to advances and breakthroughs in scientific research.

from the website: "The Moffitt Cancer Center and Research Institute Foundation was founded in 1994 to support Moffitt’s cancer research, patient care and education initiatives"

The Foundation Fighting Blindness, Inc. is the world’s leader in providing awareness and funding that drives the research that will provide preventions, treatments and cures for people affected by retinal degenerative diseases.

The Foundation's mission is to raise funds that advance scientific research into the causes, treatments and prevention of ALS; provide people living with ALS, their families and caregivers exceptional clinical care and support services; and increase awareness and eduction of ALS.

Hearts of Epilepsy Foundation® - is a registered 501(c)(3) non-profit organization. We are dedicated to providing effective tools and programs to improve the quality of life for children and families living with epilepsy. Hearts of Epilepsy Foundation participates in local and national epilepsy awareness. We provide individualize – age based support groups, individual counseling, educational and safety programs. These programs will bring great hope to those living with epilepsy. During this process - we will continue to work to reaffirm existing and develop new relationships with service providers, community organizations, and volunteers who are excited about further collaboration and committed to improving the epilepsy health in our community.

The Children's Brain Tumor Foundation is a non-profit organization founded in 1988 by dedicated parents, physicians and friends. Our mission is: to improve the treatment, quality of life and the long term outlook for children with brain and spinal cord tumors through research, support, education, and advocacy to families and survivors.

National Breast Cancer Foundation's (NBCF) mission is to save lives through early detection and to provide mammograms for those in need.Our mission includes increasing awareness through education, providing diagnostic breast care services for those in need, and providing nurturing support services.

Sankara Eye Society, Coimbatore was started in India in 1977. This trust had the philanthropic philosophy of providing high quality health care, especially eye care to all, either free or at an affordable cost. In 1998, Sankara Eye Foundation was established to support the work of Sankara Eye Society. Our mission is to attain 20/20 by the year 2020.

The mission of the Lung Cancer Research Foundation is to support national research studies and activities focused on developing innovative strategies for better treatments, screening, and prevention of all cancers of the lung. New knowledge gained by funding scientific and clinical research initiatives will lead to more positive outcomes and improved quality of life for all lung cancer patients.

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.