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To empower a nation of allies who work with us to provide support for patients and families, caregivers, and survivors; to raise awareness of preventive measures; and inspire efforts to fund critical research. Join our #NationOfAllies and find out how you can make a difference today. Because Tomorrow can’t wait™

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.

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.

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 American Institute for Cancer Research (AICR) champions the latest and most authoritative scientific research from around the world on cancer prevention and survival through diet, weight and physical activity, so that we can help people make informed lifestyle choices to reduce their cancer risk.

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!

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

Gilda's Club Madison creates a community of free emotional support, cancer education, and hope for children and adults with any cancer diagnosis and those who care for them.

National Brain Tumor Society is fiercely committed to finding better treatments, and ultimately a cure, for people living with a brain tumor today and anyone who will be diagnosed tomorrow. This means effecting change in the system at all levels.

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 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.

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.