Strategic Plan 2015 – 2018

In November 2015, the board and staff of the I.H.S. completed a new Strategic Plan to run from 2015 to 2018. 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.

There are four goals in the Strategic Plan as follows:

  • The provision of optimum support and services for all people with haemophilia and related bleeding disorders and their families.


  • To represent the interests of people with haemophilia with all external bodies and agencies.


  • To ensure the viability and development of the organisation in the future.


  • To ensure the Society plays a full and active role in the development of haemophilia care globally.