As the partner of a person living with haemophilia, you are likely to be aware of their regular appointments with their specialist healthcare team at a haemophilia centre.

Although these can often seem like routine check-ups, they are an opportunity for your partner to get involved in making decisions about their health. These decisions may help your partner to get the most out of life.¹

There are ways you can support these conversations. This downloadable booklet provides some tips on how you can help your partner get the most out of their appointments.

Reference: 1. Fong J, Annat DS and Longenecker N. Doctor-patient communication: a review. Ochsner J. 2010;10(1):38–43.