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The Bone Marrow & Cancer Foundation, founded in 1992, is dedicated to improving the quality of life for cancer and transplant patients and their families by providing vital financial assistance, comprehensive resources, educational information, physician referrals, and emotional support programs. Guided by a medical advisory board of nationally-recognized cancer specialists and working with hospitals across the United States, the Bone Marrow & Cancer Foundation is the only organization of its kind that does not limit assistance to a specific disease, type of transplant or age range. For the past 28 years, the Foundation has connected patients and their families with the services they need—from diagnosis through survivorship—to make effective decisions about treatment and its aftermath.

The organization conducts research and clinical trials to develop personalized, regenerative and immunotherapy-based treatments for brain tumors (with a focus on gliomas). It aims to accelerate curative therapies by combining personalized medicine, artificial intelligence, and patient engagement networks to translate research into clinical care.

The Myelodysplastic Syndromes Foundation was established by an international group of physicians and researchers to provide an ongoing exchange of information relating to MDS. Until the Foundation was set up, no formal working group had been devoted to MDS. Since its inception, we have conducted 14 international symposia. A major Foundation effort is our international information network. This network provides patients with referrals to Centers of Excellence, contact names for available clinical trials, sharing of new research and treatment options between physicians, and extension of educational support to physicians, nurses, pharmacists and patients.

Family Reach is a national nonprofit that provides critical financial support to cancer patients and their families, who often have to choose between treatment and daily living essentials like food or electricity. Family Reach works with patients and healthcare professionals at more than 400 top-tier hospitals and cancer centers to reach families before they hit critical financial breaking points.

"Our mission is to raise funds to support ovarian cancer research, to promote education and awareness, and to help to provide comfort to women and their families devastated by cancer."

The foundation is a patient-led nonprofit that raises awareness about inflammatory breast cancer, provides education and support to patients and families, and funds patient-focused research and biobanking to improve diagnosis, treatment, and outcomes.

The TaTa Sisterhood Foundation supports women diagnosed with triple‑negative breast cancer by providing emotional, practical, and financial assistance (care packages, connections, and short‑term aid) while also fundraising to support TNBC research.

The Cancer Council of Reno County helps people and families in Reno County affected by cancer by providing local financial and practical support (for example travel and medication assistance), operating equipment/loan programs, and promoting cancer education and prevention in the community.

The foundation works to raise awareness about renal medullary carcinoma (RMC), with a focus on people who carry sickle hemoglobinopathies (such as sickle cell trait) who may be at higher risk. It supports education, advocacy, peer support and research partnerships to reduce disparities and advance understanding and treatment of RMC.

ISCC's mission is to raise funds and support children with cancer by sending funds to organizations that provide assistance to impoverished children.

The mission of the MACC fund is rooted in supporting Wisconsin-based research to help find a cure and facilitate treatment for pediatric cancer and related blood disorders.

To enhance the quality of life for children with cancer and their families by providing financial assistance and compassionate support programs while advocating for increased research funds and raising public awareness.