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CLRA supports research efforts towards finding the causes and a cure for leukemia and assists families in meeting the financial obligations incurred in treatment. We strive to be at the forefront of funding medical expenses for families affected by blood cancers and supporting groundbreaking hospital research, ultimately leading to enhanced treatments and a cure.

The mission of the American Brain Tumor Association is to advance the understanding and treatment of brain tumors with the goals of improving, extending and, ultimately, saving the lives of those impacted by a brain tumor diagnosis. We do this through interactions and engagements with brain tumor patients and their families, collaborations with allied groups and organizations, and the funding of brain tumor research.

A 501(c)(3) nonprofit organization raising awareness and funds for new global, cutting-edge research to find a cure for glioblastoma. The purpose of the Glioblastoma Research Organization is to provide financial support to doctors and researchers around the world, that are working on developing cutting-edge technologies and clinical trials through research, to increase the rate of survival in patients, and find a cure for this disease.

The Jonsson Cancer Center Foundation (JCCF) was founded in 1945 by a group of volunteers dedicated to cancer research at UCLA. Their idea, using funds raised from private sources to invest in the work of promising young cancer researchers, resulted in the Seed Grant Program, which has helped the Jonsson Comprehensive Cancer Center (JCCC) break new ground in the quest to defeat cancer.

METAvivor is dedicated to the specific fight of women and men living with stage 4 metastatic breast cancer. At the time of METAvivor’s founding, no organization was dedicated to funding research for the disease and no patient groups were speaking out about the dearth of stage 4 cancer research. While more and more people have taken up the cry for more stage 4 research, METAvivor remains the sole US organization dedicated to awarding annual stage 4 breast cancer research.

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.

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 V Foundation for Cancer Research was founded in 1993 by ESPN and the late Jim Valvano, legendary North Carolina State University basketball coach, and ESPN commentator. The V Foundation has funded over $310 million in game-changing cancer research grants nationwide through a competitive process strictly supervised by a world-class Scientific Advisory Committee. Because the V Foundation has an endowment to cover administrative expenses, 100% of direct donations are awarded to cancer research and programs. The V team is committed to accelerating Victory Over Cancer®. To learn more, visit v.org.

Alex’s Lemonade Stand Foundation (ALSF) is changing the lives of children with cancer by funding impactful research, raising awareness, supporting families and empowering everyone to help cure childhood cancer. When Alex, who was diagnosed with childhood cancer just before her first birthday, was 4, she told her parents she wanted to set up a front yard lemonade stand. Her plan: to give the money to doctors to help them find a cure. Her first “Alex’s Lemonade Stand,” held with the help of her older brother Patrick, raised an astonishing $2,000 in one day. While bravely fighting her own cancer, Alex continued to set up lemonade stands every year. As news spread of the remarkable girl so dedicated to helping other sick children, people everywhere were inspired to start their own lemonade stands — donating the proceeds to her cause. In 2004 when Alex passed away at the age of 8 — her stand and inspiration had raised more than $1 million towards finding a cure for the disease that took her life. Alex’s Lemonade Stand Foundation (ALSF) was started by her parents in 2005 to continue the work that Alex began. Our mission is simple: to change the lives of children with cancer through funding impactful research, raising awareness, supporting families and empowering everyone to help cure childhood cancer. Since Alex set up her first lemonade stand in 2000 — truly exemplifying the saying “When life hands you lemons, make lemonade” — we have raised more than $250 million. That money has helped to: - Fund more than 1,000 cutting-edge research projects at nearly 150 institutions. - Create a Travel For Care program to help support families of children receiving treatment and develop resources, such as our SuperSibs program to help people everywhere affected by childhood cancer. Alex’s Lemonade Stand Foundation is the living embodiment of Alex’s spirit of determination and hope. Like Alex, we believe that every person can make a difference. Together, we can bring about a cure. Please join us in “making lemons into lemonade” today!

The Children's Tumor Foundation is a not-for-profit organization dedicated to finding effective treatments for the millions of people worldwide living with neurofibromatosis (NF), a term for three distinct disorders: NF1, NF2, and schwannomatosis.  NF causes tumors to grow on nerves throughout the body and can lead to blindness, bone abnormalities, cancer, deafness, disfigurement, learning disabilities, and excruciating and disabling pain.   NF affects one in every 3,000 people, more than cystic fibrosis, Duchenne muscular dystrophy, and Huntington’s disease combined.  The Children’s Tumor Foundation funds critical research into neurofibromatosis.  In addition to benefiting those who live with NF, this research is shedding new light on several forms of cancer, brain tumors, bone abnormalities, and learning disabilities, ultimately benefiting the broader community.

Our mission: Save more lives by fueling the discovery and development of powerful immunotherapies for all types of cancer. After decades of investigation, scientists have unlocked the power of our body's own immune system to fight cancer. This class of treatments—called cancer immunotherapy—enhances a patient's immune system to identify and eliminate cancer cells, anywhere in the body. Established in 1953, the Cancer Research Institute (CRI) is a 501(c)(3) nonprofit organization that is dedicated to saving more lives by fueling the discovery and development of powerful immunotherapies for all types of cancer. We fund the most innovative clinical and laboratory research around the world, support the next generation of the field's leaders, and serve as the trusted source of information on immunotherapy for cancer patients and their caregivers. CRI's programs provide strategic support along the entire pathway of discovery, drug development, and patient support.

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!