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The Tennessee Hemophilia & Bleeding Disorders Foundation is dedicated to advocacy for and support of individuals and their families with hemophilia, related bleeding disorders and complications of those disorders or their treatment, including HIV infection. The Foundation seeks to improve the quality of life of all those affected through the promotion and support of patient, public and professional education, counseling, research and other services so that each can fulfill his or her maximum potential.
The Tennessee Hemophilia & Bleeding Disorders Foundation targets assistance and support to an often overlooked community of people. Here are some of the ways that THBDF supports the Tennessee bleeding disorders community: Case Management Services. Toll-Free Helpline Number. Patient, Family, Public and Professional Education. Advocacy and Awareness. Support for Protective Legislation. Information and Referrals. Assistance with Emergency Needs. Scholarship/Enrichment Programs. Summer Camp for Boys and Girls Ages 7-15. First Step/Parents Reaching Out Program. Kids on the Block Hemophilia Puppet Show. Quarterly Newsletter. . . and more!
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