Today is World Hepatitis Day

Posted: Wednesday, 28 July 2021
Today is World Hepatitis Day! 
Please check out our Facebook page or Instagram to see tour important messaging around Hepatitis and Liver Health.
Gavin Finkelstein, HFA President, shares his story of living with hep C, treatment, finally a cure and following up his liver health. 'I was cured – it was fantastic. Hep C treatment was the best thing I ever did.' #HepCantWait

#WorldHepatitisDay @worldhepatitisalliance

COVID-19 vaccine FAQs (June 2021)

Posted: Monday, 7 June 2021
With the rollout of the COVID-19 vaccine commencing in Australia, members of the community have asked HFA about how this will impact on people with bleeding disorders.
The Australian Haemophilia Centre Directors’ Organisation (AHCDO) has endorsed the joint COVID-19 vaccination guidance for people with bleeding disorders, produced by the World Federation of Hemophilia (WFH), European Association for Haemophilia and Allied Disorders (EAHAD), European Haemophilia Consortium (EHC), and U.S. National Hemophilia Foundation (NHF). This has detailed information and is available on the AHCDO website - CLICK HERE

AHCDO has advised HFA on some answers to some common questions.

These FAQs may be updated as more information becomes known.

COVID-19 vaccine FAQs 


Posted: Saturday, 5 June 2021
Prior to the current 4th Melbourne Covid-19 lockdown, HFV staff and committee had been busy scheduling member events for the coming months.

We still hope to be able to run these events but advise members to keep checking our website for any changes to event dates. All events require booked in through Trybooking so once you have booked in for an event  you will recieve an email if there have been any changes to that event. 

Stay safe.

The HFV team

Check out the Winter edition of THE MISSING FACTOR

Posted: Friday, 4 June 2021
We are very lucky to have so many member stories in this edition of The Missing Factor. You can read about how Lenny has adapted to change. Rebecca's had a long family journey with haemophilia and now has now found much happines in her garden sanctuary! We hear from Bailey about what it is like to grow up with moderate haemophilia and Ayub shares his stroy, family history and high hopes for the future.

Latest edition of THE MISSING FACTOR available

Posted: Saturday, 6 March 2021
The latest edition of our magazine The Missing Factor is now available!
Click here to read it now.


Posted: Thursday, 11 February 2021
HFV Committee is very disappointed to announce that the Community Camp scheduled for the weekend of March 12-14 has been postponed

The Hotel Quarantine Covid case late last week has illustrated to committee just how dangerous and unpredictable these new Covid strains in particular can be and how quickly DHHS regulations restricting gathering numbers can and need to be in place.  Accordingly, in the interests of keeping our community safe and well and to ensure we can run a full camp program with unrestricted numbers, committee has decided that it would not be appropriate to hold our camp in March as originally hoped and planned.   

We are however excited to announce a new proposed camp date on the weekend November 19-22 at Lake Dewar.  By this time committee anticipate that the Australian vaccine rollout will have been completed and community gatherings will once again be quite safe.  We will look forward to seeing you all then.  And in the meantime, be sure to keep an eye out for the HFV Magazine as well as HFV on Facebook and Instagram for the latest news and announcements about related health issues and upcoming HFV programs and services.

 Thank you for your understanding and please stay safe!


Posted: Tuesday, 15 December 2020


Posted: Saturday, 26 September 2020
Wonderful news for our community this morning. This statement below is from HFA.

We are delighted that the Federal Minister for Health, The Hon. Greg Hunt MP, has announced today that emicizumab (Hemlibra®) will be publicly funded as a treatment for Australians with haemophilia.
Hemlibra® is a treatment that can reduce or stop bleeding in people with severe or moderate haemophiia A with and without inhibitors.
Gavin Finkelstein, HFA President, said, 'this is great news for our community. We are pleased all governments in Australia have agreed to fund their share of the costs of this treatment product for those in our community who need it'.
Minister Hunt said in his press release that regular supply of Hemlibra® is expected to be available by December 2020.

Click here to read Minister Hunt's press release
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WFH SUMMIT - Free Registration

Posted: Saturday, 13 June 2020
June 14 to 19, 2020

National Blood Donor Week

Posted: Saturday, 13 June 2020
Celebrating National Blood Donor Week

Getting SOCIAL on Facebook & Instagram

Posted: Monday, 1 June 2020
Keep up to date with our HFV member activities and support through Facebook and Instagram!
Making it easier to stay CONNECTED, SUPPORTED AND EMPOWERED together!
Facebook - Haemophilia Foundation Victoria
Instagram - haemophiliafoundationvictoria



Posted: Friday, 17 April 2020
Celebrating 30 years of World Haemophilia Day!

COVID-19 Update from HFA - 3rd April 2020

Posted: Friday, 3 April 2020
Important update from HFA including information about treatment and deliveries.

COVID-19 Update from HFA

Posted: Thursday, 19 March 2020
Please click on the link for an update from HFA on Covid-19


Posted: Monday, 16 March 2020
HFV member events / peer support have been POSTPONED.


Posted: Sunday, 15 March 2020
2020 Men's Retreat POSTPONED.

HFV Membership Engagement Survey

Posted: Monday, 9 September 2019
Please click here to complete this important survey and help HFV to improve our member engagement! All completed surveys go into the draw to win 2 GOLD CLASS MOVIE TICKETS!

Men's Hydrotherapy Program!

Posted: Sunday, 1 September 2019
HFV are looking for expressions of interest from men interesting in attending a hydrotherapy program. Please contact the office on 9555 7595 or [email protected] if you are interested in attending!

2019 Australian Bleeding Disorders Conference

Posted: Thursday, 13 June 2019

The 19th Australian Conference on haemophilia, VWD & rare bleeding disorders will be held at the Novotel Manly, Sydney, 10-12 October 2019.

Our conferences bring together people with bleeding disorders and their families and carers,
as well as health professionals, policy makers and industry. It is a great opportunity to learn,
discuss and plan for the future.

The conference is a great opportunity for people with a bleeding disorder and their families - parents, siblings, partners – to attend, learn more information about new treatments, gene therapy, children and young people, sport and living with a bleeding disorder etc…, make connections and become better empowered about your health.

To assist, HFA has allocated funding to assist community members with expenses to attend the Conference. Please go to or or call HFA on 1800 807 173.

Conference registration subsidies will be available to assist HFV member to attend the conference. Please complete the application form or contact the HFV office on
03 9555 7595 /[email protected] 


Posted: Thursday, 24 January 2019


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