About our Chapter

Improving the health and quality of life of people suffering from an inherited bleeding disorder as well as those suffering from the consequences of a contaminated blood transfusion.

1. Enable all people suffering from a bleeding disorder to have access to optimal medical care and services.
2. Support research.
3. Defend the interests of affected individuals by maintaining a constant vigilance.
4. Provide support and education to members and healthcare professionals, and raise public awareness about our cause.
5. Work together with the Canadian Hemophilia Society.
6. Develop partnerships with the international hemophilia community.
7. Collaborate with other organizations devoted to rare blood disorders.

Program Coordinator
Geneviève Beauregard

Administrative Assistant
Christella Biha
Suheir Maari (Maternity leave)

President
François Laroche

Vice-President
David Pouliot

Treasurer
Mylene D'Fana

Secretary
Me Gérard Morency

Other directors
Martin Kulczyk
Pascal Mireault
Éric L'Hérault
Karen Fahey
Sébastien Bédard

(see in french)