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Sponsor and support research, education and treatment of cancer for the benefit of the general public.

The Bone Marrow Foundation, founded in 1992, is dedicated to improving the quality of life for bone marrow, stem cell and cord blood transplant patients and their families by providing vital financial assistance, educational information, and emotional support programs. Transplants treat over 70 life-threatening diseases including cancers and genetic disorders. The Foundation works with transplant centers nationwide and is the only organization of its kind that does not limit assistance to a specific disease, type of transplant or age range. All of The Foundation’s services are offered free to patients and their families. Patient Programs Lifeline Fund provides funding to help cover the costs of transplant-related expenses. In addition, the program leverages social media to enable patients to reach out to their family, friends and social networks for additional financial support. One-to-One Funds assist patients and their families with fundraising efforts by creating a personal fund at The Foundation. Medical & Educational Handbooks provide comprehensive patient education and resources to assist patients and family members in obtaining information regarding all aspects of transplantation. Ask the Expert enables individuals to pose questions concerning transplantation and to have them answered by healthcare professionals. SupportLine provides support services to transplant patients and their families by linking them with volunteers who have gone through the transplant experience. Survivorship Program provides support and information to post-transplant patients, their families, and caregivers as they continue to navigate their transplant journey. Survivor Telephone Support Group staffed by oncology social workers, provides bone marrow, stem cell and cord blood transplant survivors with a weekly scheduled telephone conference support group to share experiences and draw support from others. For patients one year or more post-transplant.  

The pink wig stands for power – the power to live your life and not let cancer rule. Our mission is to provide a pink wig to cancer patients and survivors as a reminder to stay strong and live your life! We also raise awareness about the importance of genetic testing and funds for cancer genetic research.

Offer support, friendship, emotional and practical assistance and encouragement to those traveling the cancer journey.

Mission Statement: To improve the lives of young women affected by breast cancer. Our services are limited to women diagnosed under 51.

To raise and distribute funds to help children fighting cancer. Our primary focus for distribution of donations is to help pay for the cost of experimental cancer treatments, resources for travel to these treatments and any meals or lodging needed while receiving them.“By The Kid, for the kids!”

To raise funds and awareness for Komen Atlanta while connecting the breast cancer and it Atlanta commmunities.

Run for the Stripes is a 501(c)(3) non-profit corporation organized and operated exclusively for charitable purposes. Run for the Stripes' mission is to raise awareness and funds for research for neuroendocrine tumor (NET) cancers. Run for the Stripes holds an annual 5k run/walk each November (Nov. 10 is National Neuroendocrine Awareness Day).

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 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.