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Items tagged 'HFA & Foundation news'

  • National Haemophilia Journal

South Australia update

  • 23 March 2021

Save the date!   We have two activities coming up for the bleeding disorders community in South Australia.     It…

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  • News & Stories

Rare Disease Day 2021

Rare Disease Day is celebrated worldwide on 28 February 2021 to raise awareness about the experiences of people with rare diseases
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  • News & Stories

COVID-19 vaccine FAQs

Answers to FAQs about the COVID-19 vaccine for people with bleeding disorders
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  • News & Stories

HFA Research Fund grants round open

A new funding round for the HFA Research Fund is now open.
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  • News & Stories

Season’s Greetings!

The HFA Council and Staff wish you a happy and safe festive season. The HFA office will close on Thursday 24 December 2020 and reopen on Monday 11 January 2021.
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  • News & Stories

Update on new treatment options

An update from HFA about the arrangements to access Hemlibra®, a treatment for haemophilia, and HFA’s ongoing work to advocate for new treatments.
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  • News & Stories

Today is the start of Bleeding Disorders Awareness Week

We’re excited to kick off Bleeding Disorders Awareness Week today!. This week is an opportunity for individuals and families like you to take part in the campaign and get involved in activities to raise awareness about haemophilia, von Willebrand disease and related inherited bleeding disorders throughout Australia.
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  • News & Stories

Hemlibra update

The National Blood Authority (NBA) released information today about the arrangements to add emicizumab (Hemlibra®) as a treatment for Australians on the National Product List.
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  • News & Stories

Hemlibra update

The National Blood Authority (NBA) released information today about the arrangements to add emicizumab (Hemlibra®) as a treatment for Australians on the National Product List.
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  • News & Stories

Hemlibra to be publicly funded

Emicizumab (Hemlibra®) will be publicy funded as a treatment for Australians with haemophilia
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