MyABDR education materials survey

Do you or your patients record bleeds and treatments with MyABDR?

What education materials would help you or patients to record?

What do you think would be useful for someone starting out?

Haemophilia Foundation Australia (HFA) is developing new education materials for MyABDR users.

We would value your ideas and feedback to develop the resources.

All personal information you include in this survey will be treated confidentially. Any feedback we show to third parties will not identify individuals but will cover the types of ideas or issues you are commenting on.

WHAT IF YOU HAVE QUESTIONS ABOUT MYABDR?

You may find that answering this survey raises questions that you want to discuss further.

Who can help you with this?

The MyABDR Support team at the National Blood Authority
T: 13 000 BLOOD (1300025663)
E: support@blood.gov.au

The haemophilia nurse or ABDR data manager at your Haemophilia Treatment Centre

You are also welcome to contact Haemophilia Foundation Australia to discuss this project further – phone 0398857800 or email socallaghan@haemophilia.org.au.

If you have any questions or concerns about this survey, please contact Natashia Coco, Executive Director, Haemophilia Foundation Australia.

E: hfaust@haemophilia.org.au T: 0398857800