The Hemophilia Society supports individuals with bleeding disorders through awareness, treatment access, education, and community programs
Ensuring essential treatments. .
Educating patients and families on care.
Building support through local initiatives.
A child or an adult with hemophilia may approach us for help. We may come across someone with hemophilia during our journey. A classmate, coworker, friend, or neighbor might have hemophilia or another bleeding disorder. Therefore, we have a moral responsibility to learn about hemophilia and other bleeding disorders. Those suffering from pain and distress due to bleeding disorders need our support and compassion.
Learn moreHemophilia is an inherited bleeding disorder in which blood does not clot properly due to low or missing clotting factors (often Factor VIII in hemophilia A or Factor IX in hemophilia B). People with hemophilia can bleed longer after injuries and may have internal bleeds, especially into joints and muscles.
Your contribution helps provide care access, education, and community programs.
Raghunandanan’s leadership, the Haemophilia Society’s Kunnamkulam chapter flourished, running rehabilitation, physiotherapy, and counselling centres for patients. Raghunandanan also played an instrumental role as a State and national leader in the Haemophilia Federation of India, raising awareness about bleeding disorders and championing the cause of those affected by them.
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