Working for the betterment of the hemophiliacs of Bangladesh
What is Hemophilia
Hemophilia 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.
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.
Our Achievements
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Patient members
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Organized Programs
Our Mission
To provide information, education, training awareness and advice for proper care to people with hemophilia and related bleeding disorders and to advocate for greater access to treatment options.
Our Vision
To take care all people with hemophilia and related bleeding disorders to alleviate pain & suffering and to be disability-free.
In Hemophilia Society of Bangladesh, we are continuously working to make a difference in the lives of those affected by hemophilia through a variety of programs and activities. Here’s a look at some of our recent highlights.