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Founded in 1991, the Virginia Breast Cancer Foundation is committed to the eradication of breast cancer through education of and advocacy for all Virginians affected by breast cancer. Educate. Advocate. Eradicate.

The mission of the Chance for Hope Foundation is to provide support services for children with cancer and their families, funding for pediatric cancer research and treatment, and educational resources to the general public regarding pediatric cancer.

Since our founding in 1979, The Skin Cancer Foundation has saved and improved lives. We empower people to take a proactive approach to daily sun protection and the early detection and treatment of skin 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.

Southwest Kids' Cancer Foundation, Inc. is an autonomous entity formed with the goal of actively preserving and advancing Arizona Camp Sunrise and Sidekicks, and to provide a safe and nurturing camp experience for area kids who have, or have had, cancer and their siblings.

Young Fighters Foundation (YFF) Fund is a non-profit organization registered with the State of PA with a mission to create awareness and raise funds for medical resource development of childhood cancer in developing countries. YFF is a 501(c)(3) tax exempt non-profit organization registered in the State of Pennsylvania.

Debbie's Dream Foundation: Curing Stomach Cancer is a 501(c)(3) non-profit organization dedicated to raising awareness about stomach cancer, advancing funding for research, and providing education and support internationally to patients, families, and caregivers. DDF seeks as its ultimate goal to make the cure for stomach cancer a reality.

The Jennie Goas Silverman Foundation was created with love by some of Jennie's closest friends to honor her spirit, sparkle and brilliance. Jennie was diagnosed with triple negative breast cancer in June of 2016 and fought a hard battle with this devastating disease until she passed away on May 20, 2017. Jennie was a special person who impacted the lives of the people she touched. First and foremost she was a daughter, sister, wife and friend, and she always took those roles seriously. Next, she was a teacher, a high school math teacher in the CPS system. She was beautiful inside and out, she was generous, she was brilliant, she was humble and she was kind. These qualities have inspired us to create this foundation and continue to help her spirit live on through philanthropy. The Jennie Goas Silverman Foundations fundraising efforts have a dual approach: 1) Raise funds to award a qualified senior year student(s) in the communities Jennie taught with a scholarship to attend a 4-year college. 2) Raise funds and awareness for Triple Negative Breast Cancer research. Through our mission we hope to give back to the community Jennie lived and worked in and continue to fight in her honor to find a cure for triple negative breast cancer.

The mission of the Children’s Oncology Group (COG) is to cure and prevent childhood and adolescent cancer through scientific discovery and compassionate care. The Children's Oncology Group Foundation enables COG's leadership, comprised of a team of doctors, nurses, laboratory scientists and other allied professionals, the ability to direct the resources raised for childhood cancer research to the areas of highest need and opportunity.

The Bone Marrow Foundation, founded in 1992, is dedicated to improving the quality of life for bone marrow, stem cell and cord blood transplant patients and their families by providing vital financial assistance, educational information, and emotional support programs. Transplants treat over 70 life-threatening diseases including cancers and genetic disorders. The Foundation works with transplant centers nationwide and is the only organization of its kind that does not limit assistance to a specific disease, type of transplant or age range. All of The Foundation’s services are offered free to patients and their families. Patient Programs Lifeline Fund provides funding to help cover the costs of transplant-related expenses. In addition, the program leverages social media to enable patients to reach out to their family, friends and social networks for additional financial support. One-to-One Funds assist patients and their families with fundraising efforts by creating a personal fund at The Foundation. Medical & Educational Handbooks provide comprehensive patient education and resources to assist patients and family members in obtaining information regarding all aspects of transplantation. Ask the Expert enables individuals to pose questions concerning transplantation and to have them answered by healthcare professionals. SupportLine provides support services to transplant patients and their families by linking them with volunteers who have gone through the transplant experience. Survivorship Program provides support and information to post-transplant patients, their families, and caregivers as they continue to navigate their transplant journey. Survivor Telephone Support Group staffed by oncology social workers, provides bone marrow, stem cell and cord blood transplant survivors with a weekly scheduled telephone conference support group to share experiences and draw support from others. For patients one year or more post-transplant.  

The Kristy Williams Memorial Foundation is a 501(c)(3) non-profit organization that was created to continue Kristy's mission of helping others in their time of need. Our goal is to provide hope and financial support to individuals with cancer as they courageously battle this illness. 100% of the donations we receive are used to help relieve the financial strain of individuals fighting brain tumors and other forms of cancer.

The goal of the Owls for Avery Foundation is to raise funds that will go directly to researchers – labs, scientists, doctors – who are studying childhood cancer. Hepatoblastoma is one of the more rare childhood cancers, affecting only about 100 children each year, therefore, receiving less clinical trials & funding. Our mission is to support the scientists who are studying Hepatoblastoma, and to help find a cure.