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Welcome to HFI,

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Hemophilia is a genetic, life threatening bleeding disorder. In persons with hemophilia (PwH) blood does not clot normally due to deficiency or absence of clotting proteins called Factors. PwH tend to bleed internally and externally even with a minor injury. The disease is a lifelong bleeding disorder, incurable in nature and a very expensive to manage in terms of medication and care. Recurrent and prolonged bleeding into joints and muscles can lead to permanent disability. Bleeding from the sensitive organs can lead even to death.

Since 1983, Hemophilia Federation India (HFI) is the only national umbrella organization in India working for the welfare of the PwH through a network of 76 chapters spread over four regions. We aim to reach out to PwH and provide total quality care, education, make treatment available at affordable cost, psycho-social support, and economic rehabilitation and thus help them in improving the quality of life without disability and free of pain.

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All donations to Hemophilia Federation India are 50% Tax Exempted under section 80G of Income Tax Act 1961.

The journey to become a Doctor was not easy.
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Meet Vinay & explore his success mantra.
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Of will, and the way ahead!
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Receipt of ICMR award by Dr Ghosh for Hemophilia Care in India
Our President, Dr K. Ghosh has been awarded by the Indian Council of Medical Research (Dr Omprakash and Kunti Oration) for his work and services rendered towards Haemophilia Care.... Read more
  WFH delegation visit to India
Reports on meeting with WHF delegation at HFI, round table conference at New Delhi, Chennai... Read more
    Raising Hope for the Hemophilia Patients of Karnataka
In Karnataka state we have 1,573 patients and seven chapters located in Bangalore, Davangere, Mysore, Manipal, Dharwad, Hassan and Gangavathi. The major challenge for these chapters is treating poor .... Read more
HFI ran for blood brothers at Delhi Half Marathon-2011
HFI participated in the Airtel Delhi Half Marathon-2011 (ADHM) held at Jawaharlal Nehru Stadium on 27th November, with the sole purpose of spreading public awareness.... Read more
Introductory Video
Be a Part of Hemophilia Movement, Save lives of Persons with Hemophilia
According to the studies, chronic shortage of clotting factor concentrates, exorbitant treatment costs and the poor economic status of patients, makes disability an inevitable consequence of haemophilia
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