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The Glioblastoma Foundation's mission is to transform the standard of care for Glioblastoma by funding new, more effective treatments, providing support to patients and families touched by the disease, and raising awareness of this rare and aggressive grade 4 brain tumor.

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.

It was 2005. Founder (and Chairman of the Board) Nancy Roach had already made immense progress in the colon and rectal cancer climate. A group of survivors, caregivers and friends and family members touched by colorectal cancer bonded together to form the first colorectal cancer non-profit — Colon Cancer Alliance. But Nancy still felt a great need. After spending time with scientists and researchers in Washington, D.C. she knew that to change colorectal cancer – she needed to change policy. And that required a group solely focused on research advocacy. She set out to form another nonprofit dedicated to getting patients’ voices to the tables where decisions are made. After making a few phone calls, she secured sponsorships and proceeded to form C3 – Colorectal Cancer Coalition (renamed to Fight Colorectal Cancer in 2011.) The group focused efforts on having patient and caregiver voices in research and policy meetings so that decision makers could hear and see those impacted by their vote. Today, Fight Colorectal Cancer is the leading patient advocacy group in colorectal cancer and an active participant in cancer research and advocacy on the Hill. We’ve grown to become an organization known for our colorectal cancer awareness, advocacy, patient education and research programs.

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™

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.

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.

To support medical RESEARCH for finding effective treatments and eventually a cure for melanoma. To EDUCATE patients and physicians about the prevention, diagnosis and treatment of melanoma. To act as an ADVOCATE for the melanoma community to raise awareness of this disease and the need for a cure.

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

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.

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.

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