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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.

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.

The Children's Tumor Foundation is a not-for-profit organization dedicated to finding effective treatments for the millions of people worldwide living with neurofibromatosis (NF), a term for three distinct disorders: NF1, NF2, and schwannomatosis.  NF causes tumors to grow on nerves throughout the body and can lead to blindness, bone abnormalities, cancer, deafness, disfigurement, learning disabilities, and excruciating and disabling pain.   NF affects one in every 3,000 people, more than cystic fibrosis, Duchenne muscular dystrophy, and Huntington’s disease combined.  The Children’s Tumor Foundation funds critical research into neurofibromatosis.  In addition to benefiting those who live with NF, this research is shedding new light on several forms of cancer, brain tumors, bone abnormalities, and learning disabilities, ultimately benefiting the broader community.

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.

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.

CLRA supports research efforts towards finding the causes and a cure for leukemia and assists families in meeting the financial obligations incurred in treatment. We strive to be at the forefront of funding medical expenses for families affected by blood cancers and supporting groundbreaking hospital research, ultimately leading to enhanced treatments and a cure.

The Children’s Grand Adventure is nonprofit organization that rewards patients of Texas Children’s Cancer Center for their successful progression from disease. These children – whose lives have been previously “put on hold,” because of the rigors of cancer treatment – experience travel, nature, education, introspection, bonding and friendship amid one of our world’s most inspiring and unforgettable settings.

Children’s Oncology Services, Inc. operates One Step Programs that give children facing cancer a chance to meet and bond with other pediatric cancer patients and survivors in a non-hospital setting. We believe that a diagnosis of cancer should not prevent a child from experiencing the simple joys of childhood. Through our programs, kids learn to challenge themselves and give each other hope, strength and understanding through shared experiences. We empower kids who have cancer, encouraging them to take on the world.

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.

CureSearch for Children's Cancer funds and supports targeted and innovative children’s cancer research with measurable results, and be the authoritative source of information and resources for all those affected by children’s cancer.

The mission of the Jeff Gordon Children's Foundation is to support children battling cancer by funding programs that improve patients’ quality of life, treatment programs that increase survivorship and pediatric medical research dedicated to finding a cure.

The Children’s Neuroblastoma Cancer Foundation (CNCF) is a non-profit national health organization committed to finding a cure for neuroblastoma through research, education, awareness and advocacy. The premier source for neuroblastoma information and resources, CNCF initiatives educate the public about a disease dramatically lacking in awareness and funding. It serves as an advocate for families, as well as a liaison between healthcare providers and families. CNCF was created in 2000 by the family and friends of Nick Tallungan, who at 10 years old, lost his courageous battle with neuroblastoma. One brave child motivated us to make a difference – for all families affected by this disease. Today, CNCF is a global foundation representing hundreds of families. Our mission: to help fund a cure for neuroblastoma. Through the generous donations of the business community, families and friends, we create resources for families, educate the public and drive greater awareness – and funding – for neuroblastoma. We provide a forum for patients and families to share their experiences. Our national educational programs bring together clinicians, researchers and medical experts to support our mission.