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The Hemophilia Association of the Capital Area works to improve the quality of life for persons and their families affected by bleeding disorders through education support and advocacy; by networking with healthcare professionals; and by increasing public awareness of bleeding disorders.
In an effort to meet the different needs of the many people affected by bleeding disorders, the Hemophilia Association of the Capital Area provides: 2 bi-monthly educational newletters, educational events and materials, summer camp for children with bleeding disorders, social gatherings for affected individuals and thier families, limited finanacial assistance, venipuncture and self-infusion classes, and funding for research. Member of CHC and CFC.
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