The Rocky Mountain Hemophilia & Bleeding Disorders Association (RMHBDA) is a nonprofit 501 (c)(3) organization, founded in 2000, and focused on consumer education, advocacy and support. We are a chartered chapter of the National Hemophilia Foundation. Our mission is to improve the quality of care and life for persons with inherited bleeding disorders, including hemophilia and von Willebrand Disease through education, peer support, and resource and referral.
Educational Services
RMHBDA provides educational materials and disseminates information about inherited bleeding disorders and their complications to consumers, health care providers, and the general public. The organization also publishes a quarterly newsletter and maintains a library of brochures, books, articles, videos, audio tapes, and contact information for other bleeding disorders contacts such as the National Hemophilia Foundation.
Peer Support
RMHBDA sponsors an annual education weekend for members, an annual family camp for affected individuals and their families, helps families arrive at their nearest satellite clinic held bi-annually (usually in June and October) by the Mountain States Regional Hemophilia and Thrombosis Center (MSRHTC), and offers a patient assistance fund that aids families in medical crisis.
Other Resources
RMHBDA maintains a listing of specialized hemophilia care and emergency clotting factory acquisition, financial reimbursement guidance, and supporting comprehensive bleeding disorders care in Montana and Wyoming.
