In early 2020, the board and staff of the I.H.S. completed a new Strategic Plan to run from 2020 to 2024. We shall adapt and tailor our work to ensure that we continue to provide the optimum information, services and support to all those with haemophilia, von Willebrand’s disease, rare bleeding disorders and their families. This new strategic plan will govern our direction and our activities for the next four years.