Disease Specific Organizations
National Brain Tumor Society (NBTS) is a leader in the brain tumor community, bringing together the best of research and patient services to be a comprehensive resource for patients, families, caregivers, researchers, and medical professionals.
The mission of The Leukemia & Lymphoma Society (LLS): Cure leukemia, lymphoma, Hodgkin's disease and myeloma, and improve the quality of life of patients and their families. LLS has dedicated itself to being one of the top-rated voluntary health agencies in terms of dollars that directly fund our mission.
The Lymphoma Research Foundation (LRF) is the nation's largest lymphoma-focused voluntary health organization devoted exclusively to funding lymphoma research and providing patients and health care professionals with critical information on the disease.
Mesothelioma can be very stressful, but we can make life after a diagnosis easier. Mesothelioma Resource Group is proud to help those with mesothelioma and their families pursue top medical and financial resources. Connect with us right now to get started.
The mission of the National Bone Marrow Transplant Link is to help patients, caregivers, and families cope with the social and emotional challenges of bone marrow/stem cell transplant from diagnosis through survivorship by providing vital information and personalized support services.
The National Marrow Donor Program (NMDP) and their Be The Match Foundation are nonprofit organizations dedicated to creating an opportunity for all patients to receive the bone marrow or umbilical cord blood transplant they need, when they need it.
The Pancreatic Cancer Action Network is a nationwide network of people dedicated to working together to advance research, support patients and create hope for those affected by pancreatic cancer.
The Sarcoma Alliance is striving to extend and improve the lives of sarcoma patients through accurate diagnosis, improved access to care, education and support. Together we can make a difference.
Sickle Cell Disease Association of America Michigan Chapter (SCDAAMI) works to maximize the quality of life of individuals living with sickle cell disease, enable individuals with sickle cell trait to make informed decisions with respect to family planning, and provide education and testing for the general public.
There is nothing small about it. For those living with small cell lung cancer (SCLC) and the family and friends who care for them, the experience can be overwhelming – emotionally, socially and physically. Despite these challenges, you may find strength and feel more in control of the experience through access to helpful information, personalized support and community resources. We invite you to learn from – and become inspired by – others like you in this remarkable, resilient community. You are not alone.
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