Vision
An empowered, inclusive community where people with hemophilia live with dignity, safety, and real access to quality care.
“Together, we build a world where no one lives in fear of bleeding.”
About HSA
A community where no one with hemophilia feels invisible.
Our story
Built for fighters. Run by people who care.
Hemophilia Society Azamgarh exists so rare bleeding disorders don’t become lonely battles. We spread understanding, unlock care pathways, and walk with families — medically, emotionally, and socially.
We work with doctors, hospitals, and the Hemophilia Federation (India) to bring grassroots support to Azamgarh and surrounding regions.
Mission
- Spread knowledge on identification & management
- Offer counseling and social support
- Make preventive care reach those who need it
- Partner with hospitals, NGOs & government
Leadership
President — Mr. Dhirendra Jaiswal
Secretary — Mr. Vivek Mishra
Guided by volunteers and health professionals who chose action over silence.
On the ground
Programs that move the needle
- Awareness events & educational workshops
- World Hemophilia Day (17 April) campaigns every year
- Counseling sessions, registrations & medical support drives
- Partnerships with local institutions for stronger safety nets
Hemophilia changes more than blood — it shapes emotions, school days, and family finances. We exist so no patient feels left alone.
