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The Lymphoma Research Foundation's mission is to eradicate lymphoma and serve those touched by this disease.

National Brain Tumor Society is fiercely committed to finding better treatments, and ultimately a cure, for people living with a brain tumor today and anyone who will be diagnosed tomorrow. This means effecting change in the system at all levels.

The National Pancreas Foundation provides hope for those suffering from pancreatitis and pancreatic cancer through funding cutting edge research, advocating for new and better therapies, and providing support and education for patients, caregivers, and health care professionals.

The fundraising arm of Boston Children's Hospital.

The American Parkinson Disease Association (APDA) is the largest grassroots network dedicated to fighting Parkinson’s disease (PD) and works tirelessly to help the approximately one million with PD in the United States live life to the fullest in the face of this chronic, neurological disorder.

Dementia Society raises awareness and education across the United States and Canada for the syndrome known as Dementia (including Alzheimer's disease, Vascular Dementia, Lewy body, FTD, and other causes). We connect families to local resources; create meaningful therapeutic moments for those living with Dementia and their caregivers through non-medical programs that include music, movement, and the arts. We recognize and invest in outstanding Dementia care, innovation, and research.

About the CHOP Foundation: The Children's Hospital of Philadelphia Foundation is a charitable, tax-exempt organization benefiting the children's hospital of Philadelphia. As a nonprofit organization, children's hospital relies on donations to make a difference in the lives of children, to research better treatments for the future, to help families that cannot afford healthcare, and to provide quality of life programs and services.

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.

Through our exceptional health care services, we reveal the healing presence of God.

Founded in 1988 by Paul Newman, The Hole in the Wall Gang Camp is a community dedicated to providing “a different kind of healing” to children and their families coping with cancer, sickle cell anemia, and other serious illnesses. Through summer sessions and family weekends at the Camp in Ashford, Connecticut and year-round outreach to hospitals and clinics across the Northeast, the Camp serves more than 20,000 children and family members annually. All services are provided free of charge.

Assist ME enhances the lives of people with low-to-no insurance in the Charlotte metro and surrounding communities who have lost mobility by providing them with the mobility equipment they need to regain their independence. Our goal is to help those in need get back to doing the things they love and living life to the fullest. Double your donation! Check your place of business policy for matching donations and request Assist ME be added to the deserving nonprofits that can be matched.

The Glioblastoma Foundation's mission is to transform the standard of care for Glioblastoma by funding new, more effective treatments, providing support to patients and families touched by the disease, and raising awareness of this rare and aggressive grade 4 brain tumor.