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Texas Scottish Rite Hospital for Children (TSRHC) is a leading pediatric care center specializing in the treatment of orthopedic conditions, related neurological disorders and learning disorders, like dyslexia. Our mission is to improve the lives of children by providing exceptional medical care, facilitating innovative professional education programs and conducting cutting-edge research in the field of pediatric orthopedics. Since our opening in 1921, TSRHC has touched the lives of more than 225,000 children, regardless of any family's ability to pay.
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.
Golden Heart Ranch (GHR) provides young adults with intellectual and development disabilities opportunities to reach their fullest potentials and enjoy meaningful, satisfying and joyful lives. We are an inclusive community where all young adults learn, work and create lifelong friendships in a supportive and caring environment.
The mission of Hearing Health Foundation (formerly called Deafness Research Foundation) is to prevent and cure hearing loss through ground breaking research.
Your support makes it possible for us to offer high-quality patient education from top scleroderma experts, facilitate patient support groups and fund promising research.
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 CDC Foundation helps the Centers for Disease Control and Prevention (CDC) and the public health system save and improve lives by unleashing the power of partnerships to protect communities, everywhere.
Founded in 1990, the International Myeloma Foundation (IMF) is the oldest and largest myeloma-specific charity in the world. With more that 350,000 members in 140 countries, the IMF serves myeloma patients, family members, and the medical community. The IMF provides a wide range of programs in the areas of Research, Education, Support and Advocacy.
Our mission: Save more lives by fueling the discovery and development of powerful immunotherapies for all types of cancer. After decades of investigation, scientists have unlocked the power of our body's own immune system to fight cancer. This class of treatments—called cancer immunotherapy—enhances a patient's immune system to identify and eliminate cancer cells, anywhere in the body. Established in 1953, the Cancer Research Institute (CRI) is a 501(c)(3) nonprofit organization that is dedicated to saving more lives by fueling the discovery and development of powerful immunotherapies for all types of cancer. We fund the most innovative clinical and laboratory research around the world, support the next generation of the field's leaders, and serve as the trusted source of information on immunotherapy for cancer patients and their caregivers. CRI's programs provide strategic support along the entire pathway of discovery, drug development, and patient support.
The V Foundation for Cancer Research was founded in 1993 by ESPN and the late Jim Valvano, legendary North Carolina State University basketball coach, and ESPN commentator. The V Foundation has funded over $310 million in game-changing cancer research grants nationwide through a competitive process strictly supervised by a world-class Scientific Advisory Committee. Because the V Foundation has an endowment to cover administrative expenses, 100% of direct donations are awarded to cancer research and programs. The V team is committed to accelerating Victory Over Cancer®. To learn more, visit v.org.
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.