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The National Pediatric Cancer Foundation (NPCF) is a nonprofit organization dedicated to funding and developing novel research and clinical trials to find less toxic, more effective treatments for childhood cancer. Our purpose is to reduce the side effects of current treatments, improve survival rates, and ultimately eliminate childhood cancer. NPCF is a nonprofit organization under section 501(c)(3) of the Internal Revenue Code. At the National Pediatric Cancer Foundation, we are aggressively pursuing measurable change in how pediatric cancer research is approached and funded through our collaborative research consortium, the Sunshine Project. The Sunshine Project’s one-of-a-kind research model focuses on translational studies and phase 0, 1, and 2 clinical trials that address a multitude of different pediatric cancers. Our innovative approach capitalizes on the strengths of researchers from various scientific fields throughout the country, streamlining the protocol development process to deliver more personalized medicine to children with cancer. This utilization of scientific and philanthropic partnerships allows us to fast-track potential new therapies with less toxicity into clinical trials. The treatment options currently being discovered bring great promise for children who have not experienced positive results under the standard treatment protocol.

National Breast Cancer Foundation's (NBCF) mission is to save lives through early detection and to provide mammograms for those in need.Our mission includes increasing awareness through education, providing diagnostic breast care services for those in need, and providing nurturing support services.

The National Canine Cancer Foundation funds are used in eliminating cancer as a major health problem in dogs through education, outreach and research to save lives through prevention, finding cures, better treatments, more accurate cost effective diagnostic methods in dealing with cancer and diminishing dogs suffering from cancer.

The ACPMP Research Foundation is a (501(c)3) non-profit whose core mission is to: (1) Fund and support research to discover new treatments for appendix cancer with the hope of one day finding a cure. (2) Fund and support educational programs for health care professionals and patients/caregivers & families to keep pace with the evolving science and to increase awareness about this rare cancer.

Cancer Support Community San Francisco Bay Area ensures that all people impacted by cancer are empowered by knowledge, strengthened by action, and sustained by community. Cancer Support Community provides comprehensive integrative care - including counseling, support groups, nutrition, exercise and patient education programs - for people with cancer and their families or caregivers. Our services enable cancer patients to partner with their treatment team to manage their treatment and recovery most effectively, increase their chances for survival, reduce their chances of recurrence, and provide for the highest possible quality of life.

Stand Up To Cancer’s (SU2C) mission is to raise funds to accelerate the pace of groundbreaking translational research that can get new therapies to patients quickly and save lives now. SU2C brings together the best and the brightest researchers and mandates collaboration among the cancer community. By galvanizing the entertainment industry, SU2C has set out to generate awareness, educate the public on cancer prevention and help more people diagnosed with cancer become long-term survivors. Stand Up To Cancer is an initiative of the Entertainment Industry Foundation.

We raise our voice to empower and activate a community of patients, fighters and champions to push for better policies and to support research, education, and awareness for all those touched by this disease.\n\nFight Colorectal Cancer (Fight CRC) is a leading patient empowerment and advocacy organization in the United States, providing balanced and objective information on colon and rectal cancer research, treatment, and policy. We are relentless champions of hope, focused on funding promising, high-impact research endeavors while equipping advocates to influence legislation and policy for the collective good.

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 (CCF) is a global organization dedicated to curing cholangiocarcinoma (bile duct cancer) and enhancing patients’ quality of life. Through innovative methodologies, partnerships, and support programs, CCF connects patients and caregivers to resources, mentors, and support groups, while also fostering scientific discovery through an annual research fellowship program. CCF has grown to become the leading global resource in research, education, and public awareness.

To make all who are touched by invasive lobular breast cancer (also referred to as invasive lobular carcinoma or “ILC”) aware of its unique characteristics and the critical need for more ILC research; to be the go-to source for information on ILC studies, clinical trials and educational tools; to foster partnerships among patients, scientists, clinicians, and breast cancer organizations to increase dialogue about ILC and research advocacy; and to fund vital ILC research. We envision a world in which lobular breast cancer is found early, treated effectively, and eradicated permanently.

The mission of the Neuroendocrine Tumor Research Foundation is to fund research to discover cures and more effective treatments for carcinoid, pancreatic, and related neuroendocrine cancers. To achieve rapid discovery of cures, the NET Research Foundation directs its donations to fund breakthrough scientific research of neuroendocrine cancers. Since its inception, the NET Research Foundation has awarded over $22 million in large-scale, multi-year research grants to leading scientists at renowned research institutions. The NET Research Foundation is committed to improving the lives of patients, families, and caregivers affected by neuroendocrine cancer by providing information and educational resources.

The Testicular Cancer Awareness Foundation is committed to raising awareness and educating the public about the most common cancer in men ages 15–44, while providing lifesaving support to patients, survivors, and caregivers with compassion and care. Our Mission? Awareness . . Support . . Survivorship We are a nonprofit compassionately dedicated to 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, providing a resource for the medical community, providing financial assistance to those in need and continuing to save lives. We stress the importance of early detection through the practice of monthly testicular self-exams (TSE), just as women are taught to detect early signs of breast cancer through monthly breast self-exams. We are fighting to make TSE part of health education classes taught at the middle school, high school, and college levels. We seek to reduce the great stigma and taboo associated with talking about testicular health; most teenagers and young men are embarrassed to openly talk about their bodies and the changes taking place. We do this simply by talking about testicular cancer, its impacts and how to recognize the signs through regular testicular self-exams. We assist patients in seeking the most effective treatments for testicular cancer that yield the best outcomes. Testicular cancer is not as common as many of the other cancers and as a result some medical facilities are inexperienced in the treatment of this disease and may be unaware of the most effective protocols. It is crucial when diagnosed with testicular cancer that the patient has access to the most reliable and expert care that yields the best treatment plans and outcomes resulting in lifesaving measures. We seek to reduce the financial burden of a testicular cancer diagnoses by empowering the patient with resource information for financial assistance through the use of online fundraising tools. We also provide limited funding to those in immediate financial need, including helping with gas, groceries and more. We provide an online private support group to help connect those who have been affected by this disease. The role of emotional and psychological support in the management of testicular cancer is extremely important and vital to an individual's overall well-being. We have over 4,000 active members in our private support group, fostering a strong and supportive community through meaningful conversations. Our programs: Financial Assistance Program - Provides direct financial aid as well as other resources for financial assistance. Academic Education Program - Provides academic and health professionals, such as teachers, coaches, doctors and nurses with the knowledge and tools to educate students and patients about the importance of early detection of testicular cancer. Centers of Excellence - Features a comprehensive list of centers recognized for their expertise in the treatment of testicular cancer. Outreach & Awareness Program - Organizes events, fundraisers, and conferences while distributing educational materials nationwide to spread awareness. Utilizes social media as a key tool for outreach. Testicular Cancer Conferences - Brings together an international community of TC patients, survivors, and their loved ones to address the physical and emotional challenges of diagnosis and treatment at a young age. Covers life during and after cancer, lifestyle changes for healing, and features a panel of medical experts providing essential information and long-term survivorship resources. Research Studies - Collaborates with researchers to advance the understanding of testicular cancer survivorship. Today we are making a positive impact in the fight against this disease and saving lives. Visit us at www.testescancer.org to learn more!

The mission of Casting for Recovery (CfR) is to enhance the quality of life of women with breast cancer through a unique program that combines breast cancer education and peer support with the therapeutic sport of fly fishing. The retreats offer opportunities for women to find inspiration, discover renewed energy for life and experience healing connections with other women and nature. CfR’s retreats are open to breast cancer survivors of all ages, in all stages of treatment and recovery, and are free to participants. On a physical level, the gentle, rhythmic motion of fly casting is similar to exercises often prescribed after surgery or radiation to promote soft tissue stretching. On an emotional level, women are given the opportunity to experience a new activity in a safe environment amongst a supportive group of peers. The retreats provide resources to help address quality of life issues after a breast cancer diagnosis, and a new outlet – fly fishing – as a reprieve from the everyday stresses and challenges of their cancer.