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Hemophilia Society of Bangladesh supports patients with bleeding disorders through care, innovation, and community.
Patient LoginHemophilia is a rare genetic disorder that affects blood clotting. People with hemophilia lack certain proteins needed for clotting, leading to prolonged bleeding from even minor injuries. Treatment involves replacing the missing clotting factors. Understanding hemophilia helps manage the condition and prevent complications.
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We are the Hemophilia Society of Bangladesh (HSB), a charitable organization formed in 1994 by six hemophilia patients and their parents. Our mission is to provide information, education, training, awareness, and advice for proper care to people with hemophilia and related bleeding disorders. We also advocate for greater access to treatment options and quality of life for our members.
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New program updates and activities will be posted here soon.
"HSB’s medical support changed my life, giving me access to treatments I never thought possible."
–Ex Vice President, EC
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"Their awareness programs helped my family understand hemophilia better, reducing our fears."
– Member, NYC
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"Volunteering with HSB has shown me the power of community in supporting those with bleeding disorders."
– President, NYC
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