Tennessee Hemophilia and Bleeding Disorder Foundation

The Tennessee Hemophilia and Bleeding Disorder Foundation (THBDF) is a non-profit organization dedicated to improving the quality of life for individuals and families affected by bleeding disorders in Tennessee. Established in 1991, the foundation provides essential education, advocacy, and support services for conditions such as hemophilia and von Willebrand disease. THBDF collaborates with Hemophilia Treatment Centers and healthcare providers to ensure patients have access to necessary resources and specialized care. Through community events, educational seminars, and financial assistance programs, the organization fosters a supportive network for the rare disease community. The foundation also engages in legislative advocacy to protect the rights and healthcare access of those with chronic bleeding conditions.