Search Nonprofits

The Rare Cancer Research Foundation is dedicated to curing rare cancers through strategic investments and collaborations that catalyze effective research and accelerate deployment of promising therapies. Our mission is to enable rare cancer research.

The MFC Foundation is a 501 (c) 3 organization formed for the purpose providing community based social services to families living with a CANCER diagnosis. Our mission is to provide emotional, educational and financial support to families specifically for the non-medical aspects of treatment.

The mission of The Desmoid Tumor Research Foundation is to aggressively fund research to accelerate the development of improved therapies, and ultimately find a cure for desmoid tumors. We collaborate with dedicated researchers and clinicians worldwide to improve the lives of patients through education, awareness and support

Cancer Guide Research Foundation (CGRF) partners with research institutions, healthcare organizations, cancer and caregiver communities, doctors, scientists, and students to work towards helping patients understand and treat their cancer while also empowering patients by providing needed information and hope for the future.

The Ready or Not Foundation will endeavor to raise awareness of these important facts about pediatric brain cancer, and will succeed in its fundraising for leading research institutions seeking improved treatments and a cure. At this time, we are committed to funding Texas Children's Cancer Center Glioma Research program.

The Cancer Foundation for New Mexico is a local, non-profit organization supporting New Mexicans affected by cancer. Our mission is to help save lives by removing barriers and providing needed support to Northern New Mexicans with cancer seeking medical treatment in Santa Fe

The Inflammatory Breast Cancer Research Foundation's mission is to improve the lives of those touched by inflammatory breast cancer through the power of advocacy and action. We do this by fostering innovative inflammatory breast cancer research, educating stakeholders, and tirelessly advocating for both patients and survivors.

The mission of the Head & Neck Cancer Foundation is to raise awareness of this disease in our community and nation. Measurable and progressive change can be accomplished by strengthening education, awareness, research, outreach and advocacy. Our ultimate goal is saving lives and improving outcomes of those affected by head and neck cancer.

To accelerate breakthroughs, the Damon Runyon Cancer Research Foundation provides today’s best young scientists with funding to pursue innovative cancer research. We strive to: Identify the best and brightest young scientists in cancer research Accelerate the translation of scientific discoveries into new diagnostic tools and treatments Enable risk-taking on bold new ideas.

In December of 2008, Cassandra Brown, was diagnosed with this terrible disease. Although she had minor health issues, she was otherwise healthy and had no cancer-related symptoms. For more than a year, she gracefully battled on, showing her strength and being a role model to us all. Unlike many diagnosed with this disease, she was blessed with several months of happy times, leaving an everlasting footprint in the lives of those around her. In March of 2010, Cassandra’s fight was over. As a legacy to her, the Cassandra’s Cure for Cancer Foundation, Inc., a 501(c)(3) non-profit organization, was created to raise awareness and funds to help find a cure. Over the last 8 years, our foundation has raised over $70,000 through charitable events from which all proceeds were donated to the Pancreatic Cancer Action Network (www.pancan.org), the largest advocacy and medical research organization focused on finding a cure for this terrible disease.

Our mission is to take a direct and clinical approach to the prevention, early diagnosis and education of patients with prostate cancer. Genetic Testing Prostate cancer is genetically inherited and it is one of the main contributing factors in developing the disease. Our goal is to promote clinical and basic science research in genetic testing for the patients; their relatives and their descendants. The aim is to help the scientific world find the genetic signatures that predispose to the development of prostate cancer and use this to clinically impact those afflicted with and those predisposed based upon genetic heritage. Education for Patients and Physicians: The global impact of lack of education about prostate cancer is staggering. In the United States, most men diagnosed early with prostate cancer have a greater than 90% chance of cure. The majority of this is based upon early diagnosis from screening. This survival rate is not reflected worldwide. Educating patients on the virtues of regular prostate cancer screening along with their treatment options is one of our key missions. In addition, we support the education of physicians on the optimal treatment modalities. Global Screening Promoting the global screening for prostate cancer is a monumental task for any foundation. One of our key missions is to work with governments, organizations and programs worldwide and support their efforts in screening and education in their local environment.

Diseases, Disorders, Medical Disciplines