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Chai Lifeline’s guiding principles are: That seriously ill children need and deserve as happy and normal a childhood as possible; That illness affects each member of the family; That the well-being of an ill child is impacted by the well-being of his or her family; That pediatric illness can have a devastating financial effect on families. With this in mind, Chai Lifeline strives to: Find ways to bring joy to the lives of our young patients and their families through creative, innovative, and effective family-focused programs, activities, and services; Engender hope and optimism in children, families, and communities; Educate and involve communities in caring for ill children and their families; Provide unparalleled support throughout the child’s illness, recovery and beyond; Build communities among children and families living with illness or loss that allow them to engage, strengthen, and encourage one another; Offer all services free of charge to ensure that every family has access to the programs it needs.
Our mission is to empower those affected by domestic violence and advocate for social change through support, education and outreach.
Accelerate the discovery and development of drugs to prevent, treat and cure Alzheimer’s Disease, related dementias and cognitive aging.
To lead every coach and athlete into a growing relationship with Jesus Christ and His church.
To optimize philanthropy in support of the mission and future of the Children's Hospital of Chicago medical center.
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.
The Jonsson Cancer Center Foundation (JCCF) was founded in 1945 by a group of volunteers dedicated to cancer research at UCLA. Their idea, using funds raised from private sources to invest in the work of promising young cancer researchers, resulted in the Seed Grant Program, which has helped the Jonsson Comprehensive Cancer Center (JCCC) break new ground in the quest to defeat cancer.
The Foundation Fighting Blindness, Inc. is the world’s leader in providing awareness and funding that drives the research that will provide preventions, treatments and cures for people affected by retinal degenerative diseases.
To connect people with trusted breast cancer information and a community of support.
About the CHOP Foundation: The Children's Hospital of Philadelphia Foundation is a charitable, tax-exempt organization benefiting the children's hospital of Philadelphia. As a nonprofit organization, children's hospital relies on donations to make a difference in the lives of children, to research better treatments for the future, to help families that cannot afford healthcare, and to provide quality of life programs and services.
We provide hope, healing, and the best health care for children and their families. Phoenix Children's will be the premier regional pediatric center in the Southwest, nationally recognized as one of the best for pediatric care, innovative research and medical education. We will: Offer the most comprehensive pediatric care services in the Southwest region providing a full range of services solely dedicated to children Be recognized for innovative research supported by leading clinical trials of new treatment and diagnostic methods Be recognized for providing advanced education and training for clinical providers Be known as an effective advocate for Arizona’s children
The Multiple Sclerosis Association of America (MSAA) is a leading resource for the entire MS community, improving lives today through vital services and support.