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The mission of the DMRF is to advance research for more treatments and ultimately a cure, to promote awareness and education, and to support the needs and well being of affected individuals and families.

The Spastic Paraplegia Foundation is committed to promoting research to find cures for Hereditary Spastic Paraplegia and Primary Lateral Sclerosis, to educating people and their families affected by these conditions to help them live full and productive lives and to creating opportunities for mutual support and sharing

Mission: Raising a Reader supports families and inspires the development of literacy skills and a lifelong love for reading. We help children attain brighter futures in which they can thrive and contribute in school, the workforce and society. Vision: Every child has the family support and reading skills they need to thrive. Overview: Raising a Reader is a national nonprofit that partners with parents and local agencies to create brighter futures for children by strengthening family bonds. Family engagement is at the core of what we do. Our evidence-based programs help caring adults set their children up for success by creating shared reading routines, fostering social emotional learning, healthy family relationships and learning skills needed to thrive in school and beyond.

OUR GOAL IS TO IMPROVE THE QUALITY OF LIFE WITHIN RURAL NORTH CAROLINA COMMUNITIES THROUGH THE IMPLEMENTATION OF HEALTH RELATED SERVICES. WE FOCUS ON BASIC LIFE SKILLS, HEALTH PROMOTION/WELLNESS AND SELF-ESTEEM DEVELOPMENT. OUR ORGANIZATION PROVIDES RESOURCES TOWARD REMOVING BARRIERS AND INEQUALITIES TO ACHIEVE PERSONAL FULFILLMENT.

Raise crucially needed awareness of Lewy Body Dementia through the dissemination of information to health care professionals and the general public. Offer loving support and services to people with LBD and their care partners. Promote essential scientific advances and research.

To provide access to medical care, mental health services, and health and nutrition education services, regardless of the ability to pay. Their comprehensive approach helps students, parents, and the community combat the wide range of physical, psychosocial and environmental needs that arise from difficult daily living conditions in Haiti.

We are an organization created by parents of children diagnosed with rare forms of Epilepsy and Autism as a result of a change in the SCN2A gene. Our vision is to find effective treatments and a cure for SCN2A related disorders. Our mission is to improve the lives of those affected by SCN2A related disorders through research, public awareness, family support and patient advocacy. We are a registered 501(c)(3) organization.

Hip Hop Public Health creates research-based educational resources by harnessing the power of music and culture to improve health in communities that are underserved. Our vision is to achieve universal health literacy and health equity.

The Mission of the American Epilepsy Society is to advance research and education for professionals dedicated to the prevention, treatment and cure of epilepsy. As the leading multidisciplinary epilepsy professional organization, AES brings together a community of experts committed to excellence in medical knowledge, education and research dedicated to improving the live of people with epilepsy and to eradicating epilepsy and its consequences

Empower people to enhance the quality of their health and overall well-being by providing access to culturally sensitive high quality healthcare, HIV/AIDS services, health education, and social services

To lessen the demand for illicit drugs through prevention education and other effective strategies.

Our mission is to mobilize a community for patient support and advocacy, as well as drive and support impactful research that translates into advances for patients with migraine and other disabling diseases that cause severe head pain. Our core beliefs guide everything we do, from the research we promote to our efforts to build a supportive, welcoming community for all people living with migraine. Advocacy and education is the only way we will increase awareness and recognition of migraine for the disabling disease it truly is.