Who We Are
About Us:
We are the Non-Profit Organization in Lahore for all those affected by a genetic bleeding disorder; a community of individuals and families, healthcare professionals and supporters.
For over 23 years we have campaigned for better treatment, been a source of information and support, and raised the awareness of bleeding disorders.
What We Do
— Treatment
We provide quality treatment for Hemophilia in the form of Factor Concentrates.
— Counseling
We provide counseling sessions for our patients to lead a colorful life.
— Family Support
We provide monthly financial support to our needy registered patients.
— Educational Support
We provide scholarships to our bright registered patients to be successful in life and become independent.
Impact Stories
UNEXPECTED LIFE- Dr. Shahla T. Sohail
My parents were first cousins, and got married according to the cultural norms in Pakistan. At that time there was absolutely no no history of inheritance of bleeding disorder in the family.
TRAILS GIVEN TO PEOPLE ARE COMMENTSURATE TO THE COURAGE THEY HAVE- Masood Fareed Malik
Growing up in a developing country with Hemophilia meant more than discomfort, pain and disability to me. I remember the times spent lonely at home, away from friends.
RIGHT TO TREATMENT AND EMPLOYMENT- Rauf Ahmed
Living with this disease had been immeasurably harsh for me and my family. I have sent 16 years without any treatment. I’m a patient of Hemophilia “A” (Severe). we are 8 siblings, of which we twin brothers are Hemophiliacs.
Partners
