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Chai Lifeline’s guiding principles are: That seriously ill children need and deserve as happy and normal a childhood as possible; That illness affects each member of the family; That the well-being of an ill child is impacted by the well-being of his or her family; That pediatric illness can have a devastating financial effect on families. With this in mind, Chai Lifeline strives to: Find ways to bring joy to the lives of our young patients and their families through creative, innovative, and effective family-focused programs, activities, and services; Engender hope and optimism in children, families, and communities; Educate and involve communities in caring for ill children and their families; Provide unparalleled support throughout the child’s illness, recovery and beyond; Build communities among children and families living with illness or loss that allow them to engage, strengthen, and encourage one another; Offer all services free of charge to ensure that every family has access to the programs it needs.

Victory Junction enriches the lives of children with serious illnesses by providing life-changing camp experiences that are exciting, fun and empowering, at no cost to children or their families.

The Canadian Cancer Society is a national, community-based organization whose mission is the eradication of cancer and the enhancement of the quality of life of people living with cancer.

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.

The mission of The University of Texas MD Anderson Cancer Center is to eliminate cancer in Texas, the nation and the world through outstanding programs that integrate patient care, research and prevention and through education for undergraduate and graduate students, trainees, professionals, employees and the public.

Founded in 1988 by Paul Newman, The Hole in the Wall Gang Camp is a community dedicated to providing “a different kind of healing” to children and their families coping with cancer, sickle cell anemia, and other serious illnesses. Through summer sessions and family weekends at the Camp in Ashford, Connecticut and year-round outreach to hospitals and clinics across the Northeast, the Camp serves more than 20,000 children and family members annually. All services are provided free of charge.

We are a national non-profit organization compassionately dedicated in the fight against testicular cancer; through awareness and outreach, promoting the importance of monthly self-exams for early detection, support and guidance to patients and families, a resource for the medical community, providing financial assistance to those in need, and continuing to save lives.

The mission of the Lung Cancer Research Foundation is to support national research studies and activities focused on developing innovative strategies for better treatments, screening, and prevention of all cancers of the lung. New knowledge gained by funding scientific and clinical research initiatives will lead to more positive outcomes and improved quality of life for all lung cancer patients.

Be The Match Foundation supports the life-saving mission of Be The Match/National Marrow Donor Program, ensuring that patients diagnosed with blood cancers such as leukemia and other diseases get the marrow or cord blood transplant they need for a second chance at life. A transplant offers hope for a cure. We connect patients with their genetically matched donors and provide comprehensive support throughout the transplant journey, from diagnosis through recovery.

It was 2005. Founder (and Chairman of the Board) Nancy Roach had already made immense progress in the colon and rectal cancer climate. A group of survivors, caregivers and friends and family members touched by colorectal cancer bonded together to form the first colorectal cancer non-profit — Colon Cancer Alliance. But Nancy still felt a great need. After spending time with scientists and researchers in Washington, D.C. she knew that to change colorectal cancer – she needed to change policy. And that required a group solely focused on research advocacy. She set out to form another nonprofit dedicated to getting patients’ voices to the tables where decisions are made. After making a few phone calls, she secured sponsorships and proceeded to form C3 – Colorectal Cancer Coalition (renamed to Fight Colorectal Cancer in 2011.) The group focused efforts on having patient and caregiver voices in research and policy meetings so that decision makers could hear and see those impacted by their vote. Today, Fight Colorectal Cancer is the leading patient advocacy group in colorectal cancer and an active participant in cancer research and advocacy on the Hill. We’ve grown to become an organization known for our colorectal cancer awareness, advocacy, patient education and research programs.

The Pacific Mesothelioma Center at the Pacific Heart, Lung and; Blood Institute’s mission is to better serve a growing number of mesothelioma victims by supporting the first-of-its-kind in the nation research lab which provides laboratory-to-the-bedside research that improve mesothelioma victims’ lives and longevity, particularly for those that approach malignant pleural mesothelioma (MPM) as a chronic, treatable disease: The exploration of innovative ideas forms the foundation of PMC’s unique research program and provides the promise of future treatment breakthroughs. With the opening of our new laboratory at 10780 Santa Monica, dedicated solely to mesothelioma research, and by choosing specific projects, we will get closer to finding better treatments and research that we hope will eventually lead to a cure. PMC is dedicated to educating the public on asbestos-related diseases and informing them of their best treatment options. PMC also connects newly diagnosed patients with patients that have been through treatment and provides assistance and emotional support.

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.