Hemophilia is a Complex Disorder which can not be cured, but its life threatening situations can be prevented with medicine (AHF) support.
HFI does continuous advocacy and representation for Persons with Hemophilia (PwH) to improve their access to treatment and medical care.
HFI is the only National Hemophilia Federation providing education support to Children with Hemophilia (CwH).
HFI provides subsidized / free treatment support (AHF), educate and provide proper information on Hemophilia Care to both Persons with Hemophilia (PwH), their families and the medical fraternity.
HFI does awareness campaigns to make treatment available free at various state hospitals across the country.

Real Life Stories

Mahalingam, We Make Difference

We Make Difference

 

An Inspiring Story of Professional Growth with Hemophilia

 

Amit Khuva.

 

Current Newsletter

Please Make a Donation

  • All donations to HFI are 50% Tax Exempted Under Section 80G of Income Tax Act, 1961.
  • Donations towards Project on "Extending Hemophilia Care to Person with Hemophilia through Chapter Empowerment" are 100% Tax Exempted Under Section 35AC/80GGA of Income Tax Act, 1961.

News / Events

Annual General Meeting

The Annual General Meeting of HFI was held on 13th-14th, September 2014 in Kolkata, West Bengal.

The Annual G

Capacity Building Workshop

Capacity Building Workshop | 13th Sep. 2014 | Kolkata – Supported by World Federation of Hemophilia (WFH)
On 13th

WFH\HFI Advocacy Workshop

National Advocacy Prorgram With the importance of the correct method and approach of Advocacy about the cause of Hemophilia. We also appreciate the fact that