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Warrior Foundation Freedom Station’s Mission is to be the leading force in assisting, honoring and supporting the military men and women who have so bravely served and sacrificed for our country. We are committed to providing our warriors with quality-of-life items, support services and transitional housing designed to assist them and their families during recovery. Warrior Foundation Freedom Station Assists Four Main Groups of Warriors: 1. The seriously ill and injured soon to be medically retired 2. Those suffering from post-traumatic stress (PTS) and/or traumatic brain injury (TBI) 3. Those undergoing physical or occupational therapy 4. Warriors who have been medically retired and remain in our community

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.

Founded in 1997, the International Child Art Foundation (ICAF) is a 501(c)(3) nonprofit with Federal Tax ID 52-2032649. ICAF serves American children as their national arts organization and the world’s children as their global arts organization. Mission To foster American children’s creativity and develop mutual empathy among them and their peers worldwide for a prosperous and peaceful future. Vision To democratize creativity for the Fourth Industrial Revolution and grow mutual empathy for “a more perfect union.” Services ICAF organizes the Arts Olympiad, a school art program that has grown over the years into the world’s largest. Every four years, ICAF produces the World Children’s Festival as the “Olympics” of children’s imagination at the National Mall across the U.S. Capitol. Since 1998, ICAF has published the ChildArt quarterly free of commercial advertisements for children’s creative and empathic development. ICAF’s Healing Art Programs revive faith in nature of child victims of natural disasters. ICAF’s Peace through Art Programs restore trust in humanity of children living in conflict zones. To give voice to children and promote their imagination, ICAF organizes children’s panels at major conferences and interactive exhibitions that kindle professionals’ “inner child.” For children’s holistic development, ICAF has pioneered STEAMS education to integrate Art (creative activities) and Sport (physical activities) with the STEM disciplines of science, technology, engineering, and mathematics. Impact Over the past twenty-five years, ICAF has changed the world for children. More than five million schoolchildren have participated in and benefited from ICAF’s free-of-charge programs. An estimated two million students, parents, and teachers have attended ICAF festivals, exhibitions, and conferences in over twenty major cities worldwide. The readership of ChildArt quarterly has grown to an estimated 220,000. Through ICAF, children gain a sense of self-worth and confidence in themselves as creators. They come to recognize that they are the future and their imagination a seedbed for discovery and innovation. ICAF promotes their art as the most honest and pure form of human creative expression. Funding The National Endowment of the Art, the D.C. Commission on the Arts and Humanities, the Susan Zirkl Memorial Charitable Foundation, the Skillman Foundation, the Keith Campbell Foundation, and the Robert J. Bauer Family Foundation have supported ICAF this year. Current in-kind supporters include Penguin Random House, Winsor & Newtown, and Kuretake, Ltd. of Japan. Since none of the largest private foundations support ICAF, creative-empathic individuals provide the lion’s share of funding.

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.

Be The Match Foundation supports the life-saving mission of Be The Match/National Marrow Donor Program, ensuring that patients diagnosed with blood cancers such as leukemia and other diseases get the marrow or cord blood transplant they need for a second chance at life. A transplant offers hope for a cure. We connect patients with their genetically matched donors and provide comprehensive support throughout the transplant journey, from diagnosis through recovery.

The goal of Water the Seeds Foundation is to help children from no-income families reach their full potential by giving them the opportunity to pursue their education with the help of positive role models. We want to provide inspiration through our team and to show young children that education is especially important in accomplishing their life goals. We hope to improve each child’s life by keeping them involved in school, supporting their interests, and encouraging their talents.

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

The mission of the U.S. Soccer Foundation is to provide underserved communities access to innovative play spaces and evidence-based soccer programs that instill hope, foster well-being, and help youth achieve their fullest potential.We view soccer as a powerful vehicle for social change. By supporting the development of places to play, places to grow, and places to learn, our goal is to ensure that children in underserved communities have easy and affordable access to quality soccer programs that support their physical and personal development.

The Multiple Myeloma Research Foundation, Inc. mission is to: relentlessly pursue innovative means that accelerate the development of next-generation multiple myeloma treatments to extend the lives of patients and lead to a cure. To achieve this purpose, four goals are pursued: Funding research in the field of multiple myeloma, building collaborations among researchers and industry, providing disease and treatment related information to patients and family members while advocating for optimal patient care, and raising awareness of multiple myeloma.

The Maddie Potts Foundation was established in November of 2017, less than2 months after Maddie's sudden death on the soccer field of an unknown brain aneurysm. Thefoundation was founded in order to carry on Maddie's legacy of kindness, compassion, hard work,inclusive leadership and perseverance, aka Maddie Mentality. We look forward to giving back tothe community each year with scholarships, facility upgrades and opportunities for individuals ​with disabilities and eventually help change the statistics of acute death and disability of brain aneurysms through funding and research