"NO ONE SHOULD ENDURE PAIN AND SUFFERING WHEN TREATMENT EXISTS"
ABOUT HAEMOPHILIA ASSOCIATION MAURITIUS
The Haemophilia Association of Mauritius (HAM) is a Non-Governmental Organisation working on a national scale to improve and sustain treatment of people with Haemophilia and other inherited bleeding disorders.
Haemophilia is one of the most common bleeding disorders, in which the blood does not clot normally.
In Mauritius, adequate haemophilia treatment is rare and there is little infrastructure surrounding this life-threatening condition. The Haemophilia Association of Mauritius strives to ensure that one day holistic treatment for all people with bleeding disorders will be freely available and that all patients will lead a normal life.
Without treatment, most children with severe haemophilia will die young. However, with an adequate quantity of treatment products and proper care, people with Haemophilia can grow up to live healthy lives. The Association is striving towards establishing a multidisciplinary team consisting of a Haematologist, Physiotherapists, Psychologists and Nursing Officers to work together and create an effective and efficient system for the Diagnosis, Treatment, Care and Management of Haemophilia patients in Mauritius.
The members of the Association believe that ‘No one should endure pain and suffering when treatment exists’ and ‘No parent should be told that their child will die young’ The ultimate vision of the Association is to stop the bleeding so that no child born with haemophilia should have to live with pain, disability or with the prospect of early death in Mauritius.
Type of Account
Full name of Bank
Haemophilia Association of Mauritius
Mauritius Commercial Bank
Names & designations of signatories
Mr. Ramakrishna Neelayya
Mrs Sabrina Planteau de Maroussem