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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.

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.

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!

Testicular Cancer Awareness Foundation is compassionately dedicated to raising awareness and educating the general public about the most common form of cancer in men ages 15-44 and providing lifesaving valuable support for patients, survivors and caregivers. 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!

ASK is a 501(c)(3) organization founded in 1975 by a small group of parents whose children had cancer. They came together to provide mutual support, search for answers, and deal with the devastating news no parent ever wants to hear: “Your child has cancer.” With 1-2 children diagnosed per week in Central VA, your donation will be a great help to our small, local nonprofit dedicated to making life better for children with cancer. Your support will help to provide emotional, social, financial and educational care to children with cancer who are treated at the Children’s Hospital of Richmond at VCU, the only treatment facility for childhood cancer in Central Virginia. ASK provides children, siblings, and caregivers with support from the moment of diagnosis through treatment to survivorship or bereavement.

To improve the care of patients with gynecologic cancer, to advance knowledge and raise standards of practice in Gynecologic Oncology, to encourage research in Gynecologic Oncology, and, to cooperate with other individuals and organizations interested in oncology and related fields

Empower local communities to promote prevention and early detection of colon cancer and to provide support to those affected.

The Lynn Sage Breast Cancer Foundation's mission is to eradicate breast cancer by investing in early career practitioners and innovative research.

The mission of The Lustgarten Foundation is to advance the scientific and medical research related to the diagnosis, treatment, cure and prevention of pancreatic cancer; and to provide patients and families with the information they need to make informed decisions about their care.

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.

To advocate for sarcoma patients by funding research and by increasing awareness about the disease. The organization raises money to privately fund grants for sarcoma researchers and conducts education and advocacy efforts on behalf of sarcoma patients.