Through our Outreach Workers, HNZ works to support and educate members, providing information about treatment, lifestyle, risks, and the need for personal responsibility. They can also play a special role in the support of newly diagnosed families or anyone needing special assistance.

Haemophilia Outreach Workers try to visit each person with haemophilia at least once a year, with supplementary visits and calls for special needs such as hospital inpatients, extended periods away from work or school, or when confined to home. They also help plan and implement educational and social events, camps, and workshops.

Feel free to contact them with any questions or concerns you may have regarding your or your child’s bleeding disorder. We are here to help.