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The Child Cancer Fund was founded in 1994 by a group of Jacksonville, FL parents whose children were being treated for cancer; they understood the stress, anxiety and heartache of a childhood cancer diagnosis. We provide practical, emotional, financial, and educational support to children and their families every step of the way to navigate the challenges of childhood cancer.
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!
Our mission is to fund the life-saving work on childhood cancer and blood disorders at Columbia University Medical Center—including cutting-edge research, support for families, and care that always puts children first.
ASK is a 501(c)(3) organization founded in 1975 by a small group of parents whose children had cancer. They came together to provide mutual support, search for answers, and deal with the devastating news no parent ever wants to hear: “Your child has cancer.” With 1-2 children diagnosed per week in Central VA, your donation will be a great help to our small, local nonprofit dedicated to making life better for children with cancer. Your support will help to provide emotional, social, financial and educational care to children with cancer who are treated at the Children’s Hospital of Richmond at VCU, the only treatment facility for childhood cancer in Central Virginia. ASK provides children, siblings, and caregivers with support from the moment of diagnosis through treatment to survivorship or bereavement.
KrabbeConnect's mission is to be the source of comprehensive information and access to resources for patients with Krabbe disease. The foundation will drive state of the art research by bridging the gap between science and patient knowledge. The organization seeks to revolutionize the practice of medicine by identifying, optimizing, and implementing advances in the care and cure of globoid cell leukodystrophy, utilizing a multicenter network.
The mission of the NOCC is to save lives through the prevention and cure of ovarian cancer and to improve quality of life for survivors and their caregivers. Nearly 19,800+ women in the United States are diagnosed with ovarian cancer each year, and approximately 12,800+ women die from the disease. Unfortunately, most cases are diagnosed in later stages when the prognosis is poor. However, if diagnosed and treated early when the cancer is confined to the ovary, the five-year survival rate is over 90 percent. This is why it’s imperative that the early signs and symptoms are recognized not only by women, but by their families and the healthcare community.
Mission: To accelerate breakthroughs in lifesaving research and empower people everywhere to conquer cancer. Vision: Building a world where cancer is prevented or cured, and every survivor is healthy.
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 National Canine Cancer Foundation funds are used in eliminating cancer as a major health problem in dogs through education, outreach and research to save lives through prevention, finding cures, better treatments, more accurate cost effective diagnostic methods in dealing with cancer and diminishing dogs suffering from cancer.
Children's Cancer Research Fund is a national organization dedicated to curing childhood cancer by investing in the most effective research, collaborating with the most talented minds, inspiring and educating advocates worldwide to take action and supporting families.
The Children's Brain Tumor Foundation is a non-profit organization founded in 1988 by dedicated parents, physicians and friends. Our mission is: to improve the treatment, quality of life and the long term outlook for children with brain and spinal cord tumors through research, support, education, and advocacy to families and survivors.