Search Nonprofits

The Children's Tumor Foundation is a not-for-profit organization dedicated to finding effective treatments for the millions of people worldwide living with neurofibromatosis (NF), a term for three distinct disorders: NF1, NF2, and schwannomatosis.  NF causes tumors to grow on nerves throughout the body and can lead to blindness, bone abnormalities, cancer, deafness, disfigurement, learning disabilities, and excruciating and disabling pain.   NF affects one in every 3,000 people, more than cystic fibrosis, Duchenne muscular dystrophy, and Huntington’s disease combined.  The Children’s Tumor Foundation funds critical research into neurofibromatosis.  In addition to benefiting those who live with NF, this research is shedding new light on several forms of cancer, brain tumors, bone abnormalities, and learning disabilities, ultimately benefiting the broader community.

The mission of the ALS Hope Foundation is to provide long-term support to: basic and clinical research programs leading to a cure, clinical centers of excellence for the care and treatment of people with ALS, support programs for people with ALS and their caregivers that optimize care and promote independence, and programs that promote education for people with ALS and physicians about diagnosis, treatment, and care.

Committed to discovery and research, high-quality patient care and training future generations of health care leaders, we are leading the country in transforming how we take care of you to keep you well. Our goal is simple: to not only raise our standard of health care but the standard of health care. Based on Long Island, the Northwell Health Foundation serves the greater New York City Metropolitan area.

The mission of the Pulmonary Fibrosis Foundation is to accelerate the development of new treatments and ultimately a cure for pulmonary fibrosis. Until this goal is achieved, the PFF is committed to advancing improved care of patients with PF and providing unequaled support and education resources for patients, caregivers, family members, and health care providers. In pursuit of our mission, the PFF is guided by the following core values: Patient-centered Urgency Innovation Collaboration Inclusiveness Evidence-based Trusted information Compassion

Mission: To facilitate global collaboration and fund world-class research, medical education, and treatment trials, that make a positive impact on the lives of people with ME/CFS, Long COVID and related diseases. Vision: Significantly improve patient outcomes while advancing a cure. Goals: Our primary goals are to: frame clear disease mechanisms and models; find effective treatments and diagnostic markers; increase accurate diagnoses; and ensure access to quality care.

The Jed Foundation works nationally to promote emotional health and prevent suicide in student populations. To achieve this end, the organization collaborates with the public and leaders in higher education, mental health, and research to produce and advance initiatives that: Decrease the stigma surrounding emotional disorders and increase help-seeking in college and other student populations Increase understanding of the warning signs of suicide and the symptoms of emotional disorders among students Build awareness of the prevalence of suicide and emotional disorders among students Strengthen campus mental health services, policies, and programs

The mission of SSJ Health Foundation is to provide compassionate and philanthropic support for the health care ministry of the Congregation of the Sisters of St Joseph of St Augustine, Florida, to the uninsured and underserved in the Miami-Dade community. This mission is accomplished through the work of the St. John Bosco Clinic, a free clinic serving children and adults in our community. As a safety-net clinic, St. John Bosco Clinic provides primary and specialty care to those without access to health care. Our philanthropic supporters and community partners have made it possible for us to serve our community since 1992.

Our mission is to find a effective treatments and ultimately a cure for fragile X syndrome, the most common inherited cause of autism. We directly fund research grants and fellowships at top universities around the world. FRAXA was founded in 1994 by three parents of children with fragile X. Fragile X Syndrome is the most common inherited cause of autism and intellectual disabilities. It affects 1 in 4000 boys and 1 in 6000 girls worldwide, and one in 260 women and 1 in 800 men are carriers. Treatments for fragile X are likely to help people affected by related disorders including autism, Alzheimers, and many other brain disorders.

BlinkNow works to empower children and their communities in Surkhet, Nepal by funding and overseeing a children’s home, a school, a women’s center and related health and sustainability programs. The organization focuses on providing free, high‑quality education, a safe living environment for at‑risk children, and programs that promote women’s economic empowerment and community sustainability.

Their mission is to promote early detection of brain aneurysms by providing knowledge and raising awareness of the signs, symptoms and risk factors. Work with the medical communities to provide support networks for patients and families, as well as to further research that will improve patient outcomes and save lives.

Our mission is to advance the awareness and treatment of Angelman Syndrome through education and information, research, advocacy, and support for individuals with Angelman Syndrome, their families, and other concerned parties.

OMID’s mission is to support and provide tools to marginalized young women in their journey toward self-empowerment—social, economic and emotional. And to support and grow a community of clinicians, educators, who collaborate to disseminate, and implement optimal trauma treatments for these young women.