Links For Our Hematology Patients

The American Society of Hematology, the world's largest professional society concerned with the causes and treatment of blood disorders.

The Leukemia & Lymphoma Society, numerous links to other internet sites aimed at patients and medical professionals, such as other related organizations, disease specific sites, patient service and support groups, government sites, etc.

The National Hemophilia Foundation, focusing on three major strategic initiatives: research support and promotion; health education and training; and advocacy and community service.

The Aplastic Anemia & MDS International Foundation, Inc., a resource directory for patient assistance and emotional support; provides educational materials and updated medical information; and financially supports research to find effective treatment and cure for aplastic anemia & myelodysplastic syndromes.

The International Myeloma Foundation, helping everyone battling multiple myeloma—patients, families, friends, caregivers and the medical and scientific communities.

The Myelodysplastic (MDS) Syndromes Foundation, a multi disciplinary, international organization devoted to the prevention, treatment, and study of the myelodysplastic syndromes.

The American Sickle Cell Anemia Association, a nonprofit organization providing a wide range of services to those individuals and families with either sickle cell anemia, sickle cell trait, or variants of the disease.

The American Red Cross, blood, tissue, plasma and other emergency services.

The National Marrow Donor Program, helping people who need a life-saving marrow or blood cell transplant by connecting patients, doctors, donors and researchers to resources they need to help more people live longer, healthier lives.

The Fanconi Anemia Research Fund, Inc., a non-profit corporation dedicated to furthering scientific research on Fanconi anemia and providing education and support services to affected families worldwide.

The Cooleys Anemia Foundation, providing information for patients and their families, medical personnel, donors, Foundation volunteers, and anyone interested in learning about Cooley's Anemia and other forms of the genetic blood disorder, thalassemia.

The Histiocytosis Association of America, an international partnership of patients, families, physicians and friends dedicated to funding research, providing mutual support, and educating physicians and the public about histiocytosis.

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