The Haemophilia Society

About Us

Understanding Hemophilia: A Rare Bleeding Disorder

Hemophilia is a rare genetic disorder that impairs the body’s ability to form blood clots, leading to prolonged bleeding after injuries, surgeries, or even spontaneously.

While there is no cure, with proper treatment and care, people with hemophilia can lead healthy, active lives. Our mission is to ensure every patient has access to the care they deserve.

Our Global Stats

140+

Youth Group

1040+

Women’s Group

500+

States

80+

Hospitals

10,000+

Patients Supported

Our vision and mission

Hemophilia is a rare genetic disorder that impairs the body’s ability to form blood clots, leading to prolonged bleeding after injuries, surgeries, or even spontaneously.

While there is no cure, with proper treatment and care, people with hemophilia can lead healthy, active lives. Our mission is to ensure every patient has access to the care they deserve.

Rural Awareness Drive

Reaching remote communities with hemophilia education and screening programs.

Free Treatment Camps

Providing free diagnosis, treatment, and medication to underprivileged patients.

Youth Development Program

Empowering young hemophilia patients with life skills and career guidance.

Women Support Initiative

Special programs for women carriers and mothers of hemophilia patients.

Your Donation Can Save Lives

Every contribution helps us provide life-saving treatments, support patient families, and spread awareness about hemophilia. Together, we can make a difference.

5,000+

Lives Impacted

10,000+

Treatments Funded

50+

Support Centers