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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 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.  

Established in 1998, The Eye Cancer Foundation is an educational and supportive resource for eye cancer patients, their families, and physicians. Our mission is two-fold: one part focused on multi-center research of new diagnostic treatments for eye cancer research, the other focused on providing much needed, world-wide patient support services. Our mission is to create a world-class resource for patients and their families diagnosed with ocular tumors, radiation macular degeneration, and related ophthalmic conditions. We want to help you, your children and families around the world. ECF Specific Goals: 1) Find cures for patients with ocular tumors and related eye diseases. 2) Provide eye cancer specialists for unserved and underserved countries. 3) Coordinate international cooperative evaluations of new methods of diagnosis and treatment. 4) Support family and patient support programs to ease emotional stress and real-life adjustment issues related to eye cancer. 5) Promote transparency related to doctors and patient outcomes. 6) Promote quality assurance and education for eye cancer specialiatly centers. 7) Empower patients to find the resources to improve their lives.

Sponsor and support research, education and treatment of cancer for the benefit of the general public.

The Glioblastoma Foundation's mission is to transform the standard of care for Glioblastoma by funding new, more effective treatments, providing support to patients and families touched by the disease, and raising awareness of this rare and aggressive grade 4 brain tumor.

Our mission is to find a cure and improve the quality of life for those affected by cholangiocarcinoma (bile duct cancer). Founded in 2006, the Cholangiocarcinoma Foundation provides education and collaborative opportunities for patients, caregivers, doctors, researchers, industry, and other partners invested in bile duct cancer. We provide services throughout the United States and internationally. In addition to funding research, services include an annual three-day conference, complimentary publications in four languages (English, Spanish, Japanese and Chinese), a free online book "100 Questions and Answers About Biliary Cancer", an informational website, a patient registry, phone/email support and a robust discussion board.

OUR MISSION LUNGevity Foundation is firmly committed to making an immediate impact on increasing quality of life and survivorship of people with lung cancer by accelerating research into early detection and more effective treatments, as well as providing community, support, and education for all those affected by the disease. OUR VISION A world where no one dies of lung cancer. OUR VALUES We believe it's important for our board, our staff, and our constituents to know the values that drive all our actions. We are: FOCUSED ON SURVIVORSHIP 100% dedicated to increasing and improving lung cancer survivorship RESULTS-ORIENTED Always challenging the status quo and seeking a more efficient and effective way Rigorously measuring our performance to ensure maximum impact COMPASSIONATE AND RESPECTFUL Building and sustaining a community for all those affected by lung cancer Respectful of all people with lung cancer, caregivers, loved ones, medical professionals, donors, board members, and employees COLLABORATIVE Committed to being good partners and strategic collaborators to enable us to reach our goal more quickly and efficiently, including through our scientific endeavors TRANSPARENT Fiscally responsible and holding ourselves to the highest ethical standards

The mission of The Foundation for Living Beauty is to empower women to increase their physical wellness and emotional stability while coping with the taxing effects of cancer and chemotherapy.

The Rare Cancer Research Foundation is dedicated to curing rare cancers through strategic investments and collaborations that catalyze effective research and accelerate deployment of promising therapies. Our mission is to enable rare cancer research.

The MFC Foundation is a 501 (c) 3 organization formed for the purpose providing community based social services to families living with a CANCER diagnosis. Our mission is to provide emotional, educational and financial support to families specifically for the non-medical aspects of treatment.

The mission of The Desmoid Tumor Research Foundation is to aggressively fund research to accelerate the development of improved therapies, and ultimately find a cure for desmoid tumors. We collaborate with dedicated researchers and clinicians worldwide to improve the lives of patients through education, awareness and support

With a mission to find a cure for brain cancer, HOTB fundraises to support the work of world-class medical researchers and doctors, dedicated to understanding the causes and prevention of brain cancer; developing earlier detection techniques; and discovering new and improved treatments. HOTB supports the life-changing research and treatment happening at UCLA’s Jonsson Comprehensive Cancer Center and the UCLA Brain Tumor Center, which were designated a Specialized Program of Research Excellence (SPORE) in 2017 by the National Cancer Institute – one of only six brain cancer programs in the nation – recognizing UCLA’s breadth and depth in state-of-the-art, innovative, investigator-initiated translational research(bench to bedside) contributing to improved detection, diagnosis, and treatment of brain cancer. Heart of The Brain is a qualified 501(c)(3) tax-exempt organization. Tax ID #83-4187792 Together, Finding a Cure in Our Lifetime is Possible.