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Paralyzed Veterans of America (PVA), a congressionally chartered veterans service organization founded in 1946, has developed a unique expertise on a wide variety of issues involving the special needs of our members veterans of the armed forces who have experienced spinal cord injury or dysfunction. PVA will use that expertise to be the leading advocate for: - Quality health care for our members - Research and education addressing spinal cord injury and dysfunction - Benefits available as a result of our members military service - Civil rights and opportunities which maximize the independence of our members and all people with disabilities. For more than 60 years, PVA has fought for our veterans who answered the call when our nation asked for their service . . . and in return, they have given up their freedoms to protect ours.

The Carter Center, in partnership with Emory University, is guided by a fundamental commitment to human rights and the alleviation of human suffering; it seeks to prevent and resolve conflicts, enhance freedom and democracy, and improve health. Programs are directed by resident experts or fellows, who design and implement activities in cooperation with President and Mrs. Carter, networks of world leaders, other nongovernmental organizations (NGOs), and partners in the United States and throughout the world.

Unbound's mission is to walk with the poor and marginalized of the world.

THE CENTER IS A HISTORICALLY BLACK, COMMUNITY- BASED INSTITUTION SERVING MARGINALIZED EAST END CHILDREN. IT IS THE PURPOSE OF THE CENTER TO DELIVER THE HIGHEST QUALITY CHILD CARE, YOUTH AND ADULT DEVELOPMENT SERVICES TO THE COMMUNITY'S CHILDREN AND FAMILIES. WE OFFER EDUCATIONAL AND ENRICHMENT PROGRAMS FOR OUR AFTER-SCHOOL AND SUMMER CAMP CHILDREN. OUR THINKING FORWARD LECTURE SERVICES IS OPEN TO THE ENTIRE COMMUNITY.

Amani Project supports local organizations around the world to provide opportunities for young people to embrace music-making and social and emotional learning as a way to explore emotional health, connectedness, and community engagement.

To prevent the pain and trauma of burn injuries to children, and to heal, and to give children who suffered severe burns the opportunity to reach their full potential, physically, psychologically, and sociallly.

March to the Top empowers Kenyan communities by funding and partnering on projects in health, education, and conservation. We emphasize measurable, locally led solutions. 100% of donations go directly to the projects we serve, with the March Family covering all administrative costs and overhead.

Para Los Niños partners with children, youth, and their families to provide integrated early education, K–8 charter schooling, mental-health and family supports, and youth workforce services. Their work focuses on removing individual and systemic barriers so low-income children and families in Los Angeles can succeed in school and life.

Step Up is a mentorship nonprofit providing the structure for girls (and those who identify with girlhood) to define their ideal destination and get there -- wherever that destination may be. Through Step Up, girls experience more than just mentorship. They'll find community, feel empowered to expand their horizons, and develop the skills they need to navigate life’s path with confidence. After participating in Step Up: 83% of teens say they're more CONFIDENT 84% of teens say they're more CAREER-READY 82% of teens say they're more CONNECTED

To alleviate hunger through the gathering and distribution of food while encouraging self-sufficiency, collaboration, advocacy and education.

Our mission is to provide a community of healing, hope, and light throughout the life-long journey of childhood cancer. We advocate, we educate, we build partnerships, and we foster solidarity for all families experiencing cancer.Candlelighters provides support for families every step of the way from diagnosis through treatment, providing programs such as emergency financial assistance, an annual family camp, family activities, bereavement support, and a meal program that offers comfort and support for families during a difficult journey. Through it all, we never charge families a dime – ever!​

The mission of the CHARGE Syndrome Foundation: We lead and partner to improve the lives of people with CHARGE syndrome locally, nationally, and internationally through outreach, education, and research. Provide a broad network of support to individuals, families and professionals. Engage in knowledge acquisition, development and dissemination. Promote innovative scientific and clinical advancements and champion the lifelong potential of people with CHARGE syndrome. knowledgeEngage in knowledge acquisition, development and dissemination scientificPromote innovative scientific and clinical advancements championChampion the lifelong potential of people with CHARGE syndrome