The mission of the Zoefia Alexandria Foundation is to honor Zoefia’s life and her courageous battle against brain cancer. Contributions help to enrich the life of cancer children, while focusing on brain cancer advocacy and research.
Women of Color Breast Cancer Survivors Support Project
WOC is an advocacy group of breast cancer survivors, supporters, and families championing racial and economic justice in breast cancer diagnosis, treatment, and prevention for BIPOC women, while working to eliminate systemic barriers to health equity.
UCSD Moores Cancer Center
As an NCI-designated Comprehensive Cancer Center, Moores Cancer Center at UC San Diego Health is among the top 4% of approximately 1,500 cancer centers in the United States, and one of only 58 Comprehensive Cancer Centers in the nation. Approximately 43,000 patients with cancer are seen at UC San Diego Health annually. Patients have access to clinical trials with a dedicated team, as well as to physicians who provide personalized care and are setting treatment standards nationwide for more than 200 types of cancer. According to the 2025-2026 U.S. News & World Report “Best Hospitals” survey, the UC San Diego Health cancer program was ranked 42nd in the nation.
Triage Cancer
Triage Cancer® is a national, nonprofit organization that provides free education on the legal and practical issues that may impact individuals diagnosed with cancer and their caregivers, through events, materials, and resources.
The Sontag Foundation
The Sontag Foundation is a philanthropic organization accelerating breakthrough research and collaboration in brain cancer and other critical diseases. The Sontag Innovation Fund advances this mission through venture philanthropy, investing in high-impact, science-driven biomedical innovations.
The ComedyCures Foundation
Through award-winning digital and live ComedyCures programs and research studies, patients, caregivers, and healthcare workers around the world learn transformative daily coping strategies proven to decrease stress, anxiety, and depression while increasing resiliency, self-empowerment, and comic perspective.
The Brain Tumor Network
Brain Tumor Network is a national nonprofit dedicated to helping patients and families navigate the complexities of a primary brain tumor diagnosis. Founded on the belief that no one should face this journey alone, the organization provides free, personalized support to individuals across the United States. Through its navigation model, patients are connected with experienced nurse or social work navigators based on their individual needs. Navigators provide one-on-one guidance at every stage, from diagnosis through treatment and beyond. Services include helping patients understand their diagnosis and treatment options, facilitating second opinions, identifying clinical trial opportunities, coordinating medical records, and offering emotional and practical support for both patients and caregivers. As an independent and unbiased resource, Brain Tumor Network helps patients explore all available care options while feeling supported in their decisions. By combining clinical expertise with compassionate guidance, the organization empowers patients and families to move forward with clarity, confidence, and hope.
Say YES to Hope
Say YES to Hope is changing the world for those who are diagnosed with advanced cancer through outreach, education, support, and hope. We are committed to serving this underserved population of cancer patients because the association between access to care and support demonstrates increased survival, better outcomes, and improved quality of life. Our revolutionary campaigns in outreach and education help people live more fully in spite of advanced cancer and dramatically enhances the outlook for living with this life limiting diagnosis.
Rare Cancer Research Foundation
The Rare Cancer Research Foundation (RCRF) is a 501(c)3 dedicated to curing rare cancers through strategic investments and innovative collaborations that facilitate effective research and accelerate the deployment of promising therapies. Our key initiatives include pattern.org, the pattern data commons and the pattern biobank.
PALTOWN Development Foundation
PALTOWN empowers proactive patients and caregivers with educational tools and peer-to-peer support. Our programs provide connection, education, and support to thousands of colorectal cancer patients and caregivers. All our programs are created and managed by our patient and caregiver staff, who draw on their lived experience with cancer to give back in a meaningful way to their “neighbors.” PALTOWN manages the COLONTOWN colorectal cancer community, a network of 100 online groups serving thousands of patients and caregivers. COLONTOWN provides safe, private spaces for conversations around everything from managing side effects to parenting to accessing cutting edge treatments. Each group is led by trained admins with relevant lived experience. Members can belong to as many groups as fit their needs, and know that if their disease situation changes, COLONTOWN has a group to help.