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The foundation works to raise awareness about renal medullary carcinoma (RMC), with a focus on people who carry sickle hemoglobinopathies (such as sickle cell trait) who may be at higher risk. It supports education, advocacy, peer support and research partnerships to reduce disparities and advance understanding and treatment of RMC.

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 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 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 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.

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 National Breast Center Foundation exists to improve the lives of women by removing barriers that prevent them from getting proper screening, diagnosis, and education about breast cancer. Our region has the HIGHEST incidence and mortality from breast cancer in the nation. Women in our area also have one of the highest rates of late stage breast cancer. Something has to happen to address this crisis. I believe that education, access, and technology are the answer.

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.

The Snyder Nation Foundation was founded after Craig Snyder lost his valiantly fought battle against glioblastoma multiforme in 2010. Through his battle with the most lethal form of brain cancer, we learned that brain cancer is still often considered an orphan disease due to lack of funding. Our goal is help fund curative research for brain cancer, to help spread awareness of brain cancer, and to help increase access to care for those battling brain tumors.

The Surfing for Life Foundation is dedicated to bringing the surfing community together to raise awareness, inspire, and empower those touched by cancer. We are a 100% grassroots, surfer supported organization. Through our wristband program, we educate, inspire and raise awareness about cancer in the surfing community. The fundraising charity was founded in 2012 by a local surfer from Santa Barbara concerned about the widespread effects that cancer has among us all. He is committed to bringing attention to the importance of being proactive in the fight against cancer.

Founded in 1957, the Sickle Cell Disease Foundation of California is the first and oldest, non-profit, social service sickle cell disease agency in the U.S. The MISSION of the SCDFC is to provide life- enhancing programs and services to individuals with sickle cell disease, to broaden public aware- ness about sickle cell disease and to promote medical research to find a cure. Currently approximately 250 million people worldwide carry the gene responsible for sickle cell disease (SCD) and other hemoglobin diseases. Each year about 300,000 infants are born with a major hemoglobin disease worldwide. In the US, 10% of the population is at risk for SCD. It is estimated that there are approx. 5,000 persons with sickle cell disease in Los Angeles.

To raise funds and awareness for pediatric cancer research, help families battling serious medical conditions, and give back to our community.