Haemophilia Association of Mauritius

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Haemophilia Association of Mauritius HAM is dedicated to improving the quality of life of persons living with haemophilia and other inherited bleeding disorders in Mauritius

The Haemophilia Association of Mauritius is dedicated to improving the quality of life of persons living with haemophilia and other inherited bleeding disorders in Mauritius. Access to treatment is perhaps the biggest challenge facing the majority of people with haemophilia throughout the world. Only 25 per cent of those living with haemophilia are receiving adequate care. In Mauritius, adequate haemophilia treatment is rare and there is little infrastructure surrounding this life-threatening condition. The association strives to ensure that one day treatment for all people with bleeding disorders in Mauritius will be freely available.

🩸 Beyond Treatment: Strengthening Comprehensive Care in HaemophiliaToday, the Haemophilia Association of Mauritius (HAM)...
30/09/2026

🩸 Beyond Treatment: Strengthening Comprehensive Care in Haemophilia

Today, the Haemophilia Association of Mauritius (HAM) was pleased to organise a workshop bringing together nurses physiotherapists and occupational therapist to strengthen understanding and practice in haemophilia care.

The programme covered important aspects of comprehensive care:

🔹 HAM: Supporting People with Haemophilia Along Their Care Journey – Minackshi Dhurmoo

🔹 The Nurse at the Heart of Haemophilia Care – Moideen Sabeena

🔹 Beyond Factor: Understanding Comprehensive Haemophilia Care – Dr Janaki Sonoo

🔹 Protecting Movement: The Role of MSK Care in Haemophilia – Nisha Ramdin

🔹 Understanding the Person Behind the Patient: Psychosocial Support in Haemophilia Care - MohSena Olath

🔹 Joint Assessment – Jemima Kong

🙏 A big thank you to the Ministry of Health and Wellness for facilitating the release of staff to attend the workshop.

We are also grateful to the University of Mauritius for providing the venue.

This workshop was made possible through the support of our valued partner, Novo Nordisk Haemophilia & Haemoglobinopathies Foundation

Together, we continue to build knowledge, strengthen collaboration and improve comprehensive care for the haemophilia community in Mauritius. ❤️🩸

21/09/2026

Are you a healthcare professional looking to strengthen care in your country?

Applications are now open for the 2026 WFH International Hemophilia Training Centre (IHTC) Fellowships. The program offers healthcare professionals in developing countries specialized training at internationally recognized institutions, helping them bring new knowledge home to improve care.

Candidates must be nominated by their national member organization (NMO).
Learn more, hear from past fellows, and apply by November 15, 2026: https://bit.ly/4rgMGIL

🩸Haemophilia Awareness SessionAwareness session was held at Pont Colville Sub Hall, Nouvelle France, in collaboration wi...
11/09/2026

🩸Haemophilia Awareness Session

Awareness session was held at Pont Colville Sub Hall, Nouvelle France, in collaboration with the National Women’s Council.

Thank you to everyone who joined us and contributed to the discussion. 🙏

Would you like to learn more about haemophilia and bleeding disorders? Join us at our next awareness session on Tuesday, 22 September 2026 at 10:00 hrs, Midlands Village Hall.! 🩸

08/09/2026

🩸 Hémophilie : au-delà des saignements, une vie active est possible

À Maurice, 104 cas d’hémophilie ont été identifiés. Si la prise en charge a connu d’importantes avancées, des défis subsistent, notamment en matière de prévention, de suivi multidisciplinaire et d’accompagnement psychosocial.

Pour Mohsena Olath Carramtally, Operations Manager de la Haemophilia Association of Mauritius et Vice Chair du Psychosocial Committee de la World Federation of Hemophilia (WFH), il est aussi essentiel de déconstruire les idées reçues.

💬 « Une personne hémophile peut étudier, travailler, pratiquer un sport et avoir une vie active. »

Elle nous parle des progrès réalisés à Maurice, des enjeux liés à la prise en charge aux urgences et du projet de centre national de référence pour l’hémophilie.

🔗A lire sur Défi Santé : https://defisante.defimedia.info/maladies/interview-hemophilie-mohsena-olath-carramtally-notre-priorite-est-de-construire-un-systeme-de-soins-plus-structure-et-specialise/

Community Awareness🩸Awareness session with women from different localities in the South of Mauritius, focusing on haemop...
02/09/2026

Community Awareness🩸

Awareness session with women from different localities in the South of Mauritius, focusing on haemophilia and other inherited bleeding disorders.

Creating awareness, encouraging early recognition, and helping communities better understand bleeding disorders is an important part of our work at the Haemophilia Association of Mauritius.

🩸More awareness sessions are coming soon — reaching more communities.

Haemophilia Care in Emergency Departments 🩸A constructive and interactive workshop with doctors, nurses and pharmacists ...
29/08/2026

Haemophilia Care in Emergency Departments 🩸

A constructive and interactive workshop with doctors, nurses and pharmacists from all five regional hospitals, focusing on the management of people with haemophilia in Accident & Emergency Departments.

The open discussion allowed us to share real challenges faced on the ground and, most importantly, explore practical solutions to improve emergency care for our patients.

A valuable day of learning, sharing and strengthening collaboration between healthcare professionals. 🤝

A big thank you to Dr Stéphane Vanderbeeken for sharing his expertise and to all the healthcare professionals who actively participated.

Together, we continue working towards better and safer haemophilia care in Mauritius. ❤️

Stronger haemophilia care starts with collaboration. Thank you to Dr Stephane Vanderbecken, Haematologist from Réunion I...
27/08/2026

Stronger haemophilia care starts with collaboration.

Thank you to Dr Stephane Vanderbecken, Haematologist from Réunion Island, for providing specialist consultations to 25 patients across five Regional Hospitals, with the support of the Ministry of Health and Wellness.

We’re grateful to all healthcare professionals, patients and families who made this initiative possible. Together, we’re building better, more comprehensive haemophilia care in Mauritius.

💙 A meaningful day of learning, sharing, and connection.Recently, women and girls affected by bleeding disorders came to...
12/08/2026

💙 A meaningful day of learning, sharing, and connection.

Recently, women and girls affected by bleeding disorders came together for a workshop combining haemophilia carrier education and psychosocial support.

Through stories, emotions, and reflection, they shared their strength, resilience, and the power of knowing they are not alone.

Together, we continue to empower and support our bleeding disorders community. 💙

💙 A Valuable Partnership for Better Haemophilia CareThe Haemophilia Association of Mauritius was honoured to welcome the...
27/07/2026

💙 A Valuable Partnership for Better Haemophilia Care

The Haemophilia Association of Mauritius was honoured to welcome the World Federation of Hemophilia (WFH) delegation during their visit to Mauritius from 26–30 June 2026.

The visit provided an opportunity to strengthen collaboration, share expertise and discuss the future of haemophilia care, including comprehensive care models, multidisciplinary services, capacity building and improved access to treatment.

Our sincere appreciation to WFH for their continued commitment, guidance and support in advancing haemophilia care in Mauritius and across the region.

Together, we continue to make a difference for people living with haemophilia. 💙

23/07/2026

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5 A, Ibis Lane, Sodnac
Quatre Bornes

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