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Find A Cure Transit Hemophilia Resources:
Bleeding Disorders Foundation of Washington
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The Bleeding Disorder Foundation of Washington is a volunteer-based non-profit that works to improve the quality of life of individuals and families affected by bleeding disorders by providing caring support , quality education and targeted advocacy aimed at enhancing medical care and insurance coverage for our community.
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FAMOHIO is a non-profit organization that provides emotional and educational support to individuals with hemophilia and related bleeding disorders.
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The Great Lakes Hemophilia Foundation is dedicated to advancing the quality of life of individuals and families affected by hemophilia or other blood disorders by ensuring a broad range of services and programs while supporting research to improve care and to find a cure.
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The Hemophilia Foundation of Illinois exists to improve the quality of life for persons affected by inherited bleeding disorders.
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Founded in the 1950's, The Hemophilia Foundation of Maryland is the only non-profit 501 (c)(3) organization in the state of Maryland which is devoted to improving the quality of life for persons affected with bleeding disorders and their complications. The bleeding disorder community includes people with Hemophilia A, Hemophilia B and von Willebrand disease.
Hemophilia Foundation of Southern California
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Hemophilia Foundation of Southern California seeks to promote, supervise and administer the programs for the welfare of people with hemophilia, related bleeding disorders, and their families, through proper medical care, treatment, education and research.
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The Hemophilia Outreach of El Paso is a non profit 501(c)3 organization, established by volunteers, who are individuals or parents of children with Hemophilia and/or von-Willebrand. Our objective is to give all necessary educational information and emotional support to individuals and families that have a bleeding disorder.
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The Lone Star Chapter of the National Hemophilia Foundation serves the bleeding disorders community of South Texas. We are based in Houston and our area includes McAllen, Corpus Christi, San Antonio, Austin, and El Paso
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The New York City Hemophilia Chapter (NYCHC) is a non-profit 501(c)3 organization incorporated in 2008 to address the needs of the bleeding disorder community in the greater NYC area, including: Long Island, Staten Island, Westchester, Queens and Brooklyn.
Tennessee Hemophilia and Bleeding Disorders Foundation
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The Tennessee Hemophilia and Bleeding Disorder Foundation’s mission is to Enhance the Lives of Those Affected by Bleeding Disorders.
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Amy Maeder is a mother of two teenagers with severe hemophilia. Amy is very passionate about improving the lives of her sons and the bleeding disorders community. Amy, along with HFA encourages you to TAKE ACTION! Call or write your person in congress TODAY!
Find A Cure Transit Hemophilia Resources:
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