ABOUT HWSK BACKGROUND

In 2016 journey started with empty hands and pockets, so the founders had to work with a strategy to ensuring close collaboration and building strong relationships for the generation of treatment resources and facilities. They provided a platform for the entire Hemophilia Community to build strong support for the patients and have initiated multiple parents, women, and youth community groups in order to empower the patients to stand up for the Hemophilia cause. Through productive advocacy efforts involving the doctors and community, HWSK has been successful in positioning Hemophilia as a separate identity that this bleeding disorder community deserves. HWSK tackles Hemophilia rehabilitation not in terms of just treatment but rather as a holistic approach, providing a roadmap towards community strengthening. Empowering women with bleeding disorders, to understand their psychosocial issues and financial issues as they are not highlighted enough. Empowering the young bleeding disorder community by making available scholarships and micro-finance outlets so that they are not a burden for their own family. The founders were able to introduce advanced treatment products donated by WFH’s Humanitarian Aid Programs which are not available locally in the public-private sector till date. HWSK is building a network of government officials and private entities in order to highlight the fact that a dedicated Hemophilia center is the eminent need of the hour. Tirelessly reaching out to PWH to provide quality care, education, treatment availability at affordable cost, psycho-social support, and economic rehabilitation.