Search Nonprofits

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.

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 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

from the website: "Since the 2012 death of their son Trayvon Martin in a violent confrontation, Sybrina Fulton and Tracy Martin, along with their son Jahvaris, created the Trayvon Martin Foundation out of a need to bring awareness to ending senseless gun violence. By sharing their personal and powerful stories, they have encouraged diverse audiences—from college students and faculty and legal professionals to community and family organizations—to become more educated on ways to keep their loved ones safe and to empower themselves to become catalysts for social change."

The mission of the Pitt Hopkins Research Foundation (PHRF) is to support research dedicated to finding a treatment, and hopefully an eventual cure of Pitt Hopkins and other similar disorders. Made up of families for families, the PHRF is also dedicated to supporting PTHS children with resource recommendations, parental support and the latest medical information.Our board and officers are parents and professionals who volunteer their time, so that over 93% of all funds raised and donated go to finding a cure. Our goal is to find a treatment as quickly as possible that will help give our children fuller, higher functioning lives.

Children’s Hospital Colorado Foundation was established in 1978 and is dedicated solely to advancing the mission of Children’s Hospital Colorado. Thanks to donations large and small and the generous philanthropic spirit of our community, Children’s Colorado is able to provide the family-centered care for which we have become world renowned. From conducting cutting-edge research and treatment to building kids’ confidence through our hospital sports program, providing family sleep rooms and integrating arts therapy into the healing process, Children’s Colorado is truly unique in its approach to treatment.