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The mission of the Mesothelioma Applied Research Foundation (Meso Foundation) is to eradicate mesothelioma as a life-ending disease. Malignant mesothelioma is a rare cancer of the linings of the chest or abdomen. Asbestos exposure is the only known cause. The Meso Foundation solicits and rigorously reviews applications, and then awards significant grants, for research on the prevention, early detection, and treatment of mesothelioma. Through its web site and literature, its direct communications, and annual Symposium the Foundation provides patients, family members and physicians with hope, encouragement, and information. The Meso Foundation employs a full-time mesothelioma nurse practitioner to help patients navigate their treatments. In addition, the Foundation works to enhance awareness of this disease and to encourage federal funding for research.

It is our mission to aid in the fight against cancer by raising our voices in song. Through song we celebrate those we love, remember those we have lost, honor those who fight, and rejoice for those who survive. With music as our voice, we raise awareness and funds to support those who conduct the research and create the hope of finding a cure for generations to come. Our inspirational performers, whose lives have all been affected in some way by cancer, share stories of hope, loss, and courage through song, dance, and testimonials, allowing for an intimate and inspiring look at our collective fight against cancer. To that end, VOH dedicates its performances and additional fundraising efforts to this life-changing cause.

Tough2gether Foundation is fighting childhood cancer. It's personal to us! We've watched too many children die from DIPG, the most terminal childhood cancer. In fact Tough2gether Foundation was founded by Jace Ward, who at 20 fought DIPG for two years while advocating for others, raising funds to expand trials and starting this foundation. We work daily to care for families in the fight by providing information and supporting their financial needs. Central to our mission is fueling research and clinical trials and to fill the gaps in the current pediatric cancer system. We're bringing people who care together to change the patient data landscape and the way clinical trials operate from a single approach to combinations. Team up with us to end DIPG and all childhood cancer as we know it.

Ayden’s Army of Angels provides resources financial and nutritional, to any families effected by Pediatric Cancer.We also know the importance of creating memories, so we host a variety of events throughout the year, not only to bring awareness, but to provide families the opportunity to create lasting memories. Our primary funding has come from Ayden himself. Prior to Ayden’s passing we raised 265k to seek him alternative treatment. Before we could get to those options, Ayden passed. I have taken the remainder of Aydens GoFundMe and opened the Foundation. Since September of 2017, I have issued over $30k in grants to Cancer Families. We have also hosted several parties and events for the families all at no cost to them.

The purpose of the UC San Diego Foundation is to foster community support, promote philanthropic giving, invest and manage gift funds and assets, provide advice and counsel to the chancellor, and to act as advocates for the benefit of the University of California, San Diego campus, in accordance with applicable university policies, guidelines and procedures. The UC San Diego Foundation helps UC San Diego obtain private gifts (in support of research, teaching, and public service) and manages the gift assets. Moores Cancer Center's unique blend of cancer research and patient care is transforming cancer prevention, detection and treatment. Established in 1978, Moores Cancer Center at USCD is ranked among the top 50 oncology programs in the nation and is the San Diego region’s only National Cancer Institute-designated Comprehensive Cancer Center. This designation is reserved for centers with the highest achievements in cancer research, clinical care, education and community contributions.

Our mission is to take a direct and clinical approach to the prevention, early diagnosis and education of patients with prostate cancer. Genetic Testing Prostate cancer is genetically inherited and it is one of the main contributing factors in developing the disease. Our goal is to promote clinical and basic science research in genetic testing for the patients; their relatives and their descendants. The aim is to help the scientific world find the genetic signatures that predispose to the development of prostate cancer and use this to clinically impact those afflicted with and those predisposed based upon genetic heritage. Education for Patients and Physicians: The global impact of lack of education about prostate cancer is staggering. In the United States, most men diagnosed early with prostate cancer have a greater than 90% chance of cure. The majority of this is based upon early diagnosis from screening. This survival rate is not reflected worldwide. Educating patients on the virtues of regular prostate cancer screening along with their treatment options is one of our key missions. In addition, we support the education of physicians on the optimal treatment modalities. Global Screening Promoting the global screening for prostate cancer is a monumental task for any foundation. One of our key missions is to work with governments, organizations and programs worldwide and support their efforts in screening and education in their local environment.

In December of 2008, Cassandra Brown, was diagnosed with this terrible disease. Although she had minor health issues, she was otherwise healthy and had no cancer-related symptoms. For more than a year, she gracefully battled on, showing her strength and being a role model to us all. Unlike many diagnosed with this disease, she was blessed with several months of happy times, leaving an everlasting footprint in the lives of those around her. In March of 2010, Cassandra’s fight was over. As a legacy to her, the Cassandra’s Cure for Cancer Foundation, Inc., a 501(c)(3) non-profit organization, was created to raise awareness and funds to help find a cure. Over the last 8 years, our foundation has raised over $70,000 through charitable events from which all proceeds were donated to the Pancreatic Cancer Action Network (www.pancan.org), the largest advocacy and medical research organization focused on finding a cure for this terrible disease.

AIM at Melanoma is globally engaged and locally invested in advancing the battle against melanoma through innovative research, legislative reform, education, and patient and caregiver support. Founded in 2004, AIM at Melanoma is the largest international melanoma foundation seeking the cure for melanoma. We are dedicated to: Innovation in Melanoma Research We believe that the cure for melanoma will be found more quickly by bringing together leading global researchers and funding their collaborative research. Our three paradigm-shifting global research initiatives, including the Melanoma Tissue Bank Consortium, are poised to reshape the future of melanoma. Legislation, Policy & Advocacy We are the respected voice of melanoma across the nation. When drugs are approved, legislation is drafted, and research is assessed, AIM is at the table, speaking loudly and clearly on behalf of patients and their families. We are trusted advisors for pharmaceutical companies, medical boards, and government agencies on critical topics that affect melanoma patients. Information & Resources Both in the U.S. and on a global level we provide comprehensive, easy-to-access melanoma information and resources to patients and healthcare professionals.

Founded by Dr. Hadiyah-Nicole Green, the Ora Lee Smith Cancer Research Foundation is on a mission to change the way cancer is treated and reduce cancer-patient suffering by providing a treatment that is accessible, affordable, and, most importantly, effective. Despite all of modern and alternative medicine’s best approaches, nearly 9 million cancer-related deaths occur every year due to cost, access, and efficacy of current treatment options. Dr. Green has developed a new arsenal in the war on cancer, Laser-Activated Nano-Therapy (LANT). After a single 10-minute treatment, LANT completely eliminates tumors in laboratory mice in just 15 days, without any observable side effects. Limited by funding, not technological advancements, LANT is ready for human trials. The purpose of the Ora Lee Smith Cancer Research Foundation is to move LANT beyond the laboratory and into humans, independent of the pharmaceutical industry with tax-deductible donations. We have the capacity to save lives. With our revolutionary technology, we can. With your help, we will. Together, #WeAreOraLee. Together, with your generous support, we can change the way cancer is treated.

13thirty Cancer Connect is a registered 501 (c) (3) non-profit organization established in 2001 following the death of Melissa Sengbusch who was 19 years old when she died of acute myeloid leukemia. Since its beginning (first called Melissa’s Living Legacy Teen Cancer Foundation), 13thirty has become an internationally known and respected leader in the field of adolescent and young adult (AYA) cancer because of our strong passion, clear vision, and steadfast commitment to a singular focus – teens and young adults with cancer. Unlike many other cancer support organizations, we concentrate our efforts and resources on a targeted national problem that affects approximately 90,000 young people in the United States each year. As Melissa asked of her mom, we are making a difference. We are making things better for teens and young adults with cancer around the world. The MISSION of 13thirty Cancer Connect, Inc. is to help adolescents and young adults (AYAs) impacted by cancer live their very best lives – today! Our resources help AYAs enhance their coping skills and self-esteem by building satisfying peer connections, learning to self-advocate, and developing effective self-management tools for long-term health. A comprehensive continuum of support (from diagnosis and treatment to healthy survivorship or if necessary, end-of-life) helps AYAs with cancer successfully transition through each stage of their cancer experience. We advocate strongly for improved delivery of medical and educational services through clinician education initiatives and outreach to schools and universities. Together with our strategic partners, we work to increase access to age-appropriate care for all AYA patients and survivors with concentrated focus on improving survivorship (early detection, health maintenance and follow-up care).

The Mammogram Poster Girls' mission is to raise awareness and funds for the early detection of breast cancer. Funding screening mammograms for those in need.

Fund pediatric brain cancer research & support families