Our mission

OUR MISSION

The mission of the Hemophilia Society of Bangladesh is to significantly improve the quality of treatment for patients with hemophilia and other bleeding disorders in Bangladesh. By raising awareness about hemophilia, von Willebrand disease, and other bleeding conditions, we aim to educate the public and medical community. Our efforts include fostering strong collaborations with hemophilia treatment centers across Bangladesh, engaging actively with the government to advocate for better healthcare policies, and partnering with key stakeholders such as healthcare providers, pharmaceutical companies, and patient advocacy groups.

We strive to ensure that every patient with a bleeding disorder in Bangladesh receives timely and effective care. Through our initiatives, we work towards enhancing access to advanced treatment options, promoting early diagnosis, and providing comprehensive support to patients and their families. Our ultimate goal is to improve health outcomes and the overall quality of life for individuals living with hemophilia and other bleeding disorders in Bangladesh.

Key Focus Areas:

1. Awareness and Education: Increasing public and medical awareness about hemophilia and related bleeding disorders through campaigns, workshops, and educational programs.
2. Collaboration with Treatment Centers: Building strong partnerships with specialized hemophilia treatment centers to ensure high standards of care and support.
3. Government Engagement: Advocating for policy changes and government support to enhance treatment accessibility and affordability.
4. Stakeholder Partnerships: Working with healthcare providers, pharmaceutical companies, and patient advocacy groups to improve treatment options and patient support systems.

By integrating these efforts, the Hemophilia Society of Bangladesh is dedicated to making a meaningful impact on the lives of those affected by bleeding disorders, ensuring they receive the best possible care and support.