Category: National Organizations & Websites

SFA advocates to improve outcomes for people diagnosed with sarcoma by funding and advancing research, educating patients and the public, and leading advocacy efforts on behalf of the sarcoma community. The organization works to increase awareness of sarcoma, support scientific progress, and bring together a unified voice for patients, survivors, caregivers, and researchers.

An international nonprofit advocacy organization dedicated to supporting people affected by sarcoma. The organization provides guidance, education, and support to patients, caregivers, and families through accurate information, peer‑to‑peer connections, support groups, financial assistance for second opinions from sarcoma specialists, and resources to help individuals navigate diagnosis, treatment options, and access to quality care for this rare cancer.

Provides funding for research and treatment of sarcoma, the education of young physicians, and seeks to improve the quality of cancer patient life.

ZERO Prostate Cancer works to advocate its efforts towards a cancer free generation at federal and state levels, provides information for patients about treatment, and provides services to those at risk. Their mission is to improve and save lives from prostate cancer through advocacy, awareness, education, and support.

Provides prostate cancer education and risk‑awareness through a multi‑channel information model including a website, toll‑free phone line, counselors, public forums, newsletters, and community outreach. It brings education directly into community settings such as churches, service agencies, and barbershops, particularly within the Black community, to support informed health decisions and early disease awareness.

A national organization creating hope through research, patient support, community outreach, and advocacy for a cure. Committed to programs and services that provide information to patients, health professionals and the general public. They seek to advance research, support patients, and provide tools for patients looking to receive care.

A nonprofit organization focused on accelerating the development of new treatments for multiple myeloma. The foundation advances research through clinical trials, drug development, and data‑driven approaches, while providing patients and caregivers with educational resources and information about emerging therapies. Since its founding, the organization has raised hundreds of millions of dollars for myeloma research and contributed to the development of numerous FDA‑approved therapies.

A global nonprofit organization dedicated to improving outcomes and advancing a cure for multiple myeloma. IMF supports innovative research initiatives, including investigator grants and collaborative clinical research, provides extensive education through publications, seminars, videos, and patient forums, and offers patient and caregiver support through a toll‑free InfoLine, support‑group networks, advocacy programs, and global partnerships focused on access to care and awareness.

Mesothelioma Resource Online has created and developed this site to provide answers and support for people diagnosed with mesothelioma cancer, as well as their families and loved ones. They have a team of patient advocates, nursing support staff, and legal associates to assist mesothelioma patients.