Haemophilia Foundation Australian Capital TerritoryACT

Skip to content Normal contrast High contrast
Menu
MENU
Contact Us Donate
  • Home
  • About Us
    • Who We Are
      • Charitable Status Information
    • What We Do
    • Mission, Vision & Governance
      • Rules of Association
      • Strategic Plan
      • Code of Conduct
      • Conflicts of Interest
      • Complaint Resolution
    • Our Committee
      • Committee Membership
      • Committee Roles
    • Our Counsellor
    • Sponsors and Supporters
    • Working with HFA
    • Contact Us
  • About Bleeding Disorders
    • Fast Facts
    • FAQs
      • View All FAQs
    • Haemophilia
    • Von Willebrand Disease
    • Women with Bleeding Disorders
      • Haemophilia and carrying the gene
      • VWD in females
      • The Female Factors
      • Personal stories
      • Other women's resources
    • Youth with Bleeding Disorders
    • Other Bleeding Disorders
      • Factor I Deficiency
      • Factor II Deficiency
      • Factor V Deficiency
      • Combined Factor V and Factor VIII Deficiency
      • Factor VII Deficiency
      • Factor X Deficiency
      • Factor XI Deficiency
      • Factor XIII Deficiency
    • Gene Therapy
    • Hepatitis C & HIV
      • Hepatitis C
        • HFA hepatitis C strategy
        • Double Whammy Report
        • Getting It Right evaluation
        • Hep C Resources
        • Hep C Treatments
        • Hep C Personal Stories
          • Terry's Story 2010
          • Ben's Story 2010
          • Les's Story 2009
        • Telling others about hep C
      • HIV
        • HIV and Bleeding Disorders
        • Living with HIV
    • Living with a Bleeding Disorder
      • Personal Stories
        • Women
        • Hepatitis C
          • Anth's treatment story
          • Simon's treatment story
          • Len's treatment story
          • Paul's treatment story
          • David's treatment story
        • Youth
        • Newly Diagnosed
        • Living with haemophilia
        • Living with VWD
        • Growing up with a bleeding disorder
      • Disclosure
      • Travel
      • Getting Older Info Hub
    • Safety and Supply
  • Support & Services
    • Foundation Services
    • Support Groups
    • Member Benefits
    • Our Counsellor
    • Community Camp
    • Government Support
    • Community Organisations
    • ABDR & MyABDR
      • ABDR
      • What is MyABDR
      • Why use MyABDR?
      • MyABDR Updates
      • Privacy Consent
      • Background
      • Have Your Say
      • MyABDR Feedback
    • Youth
      • Youth News
      • Factored In - youth website
      • Colouring in fun!
    • Kids
      • Colouring in fun!
      • Livewire
    • State & Territory Foundations
    • Treatment Services in the ACT
      • Treatment Centres
      • Paediatric Day Stay Unit
      • Physiotherapy
      • Visiting Emergency
  • Publications
    • Introductory Brochure
    • Newsletter
      • Back Copies
    • Annual Reports
    • Information Resources
      • Bleeding Disorders
      • Haemophilia
        • Newly Diagnosed
        • Haemophilia booklets & fact sheets
        • Mild Haemophilia
        • Living with Mild Haemophilia
        • Haemophilia testing in women and girls - your questions
        • Sport
        • Gene therapy
      • Von Willebrand Disease
      • Women with Bleeding Disorders
        • Young women
        • Haemophilia testing in women and girls - your questions
        • Telling others
        • Sport and exercise for young women
      • Young People
      • Getting older
        • Getting Older Info Hub
        • For health professionals
      • Hepatitis C
        • Hep C Fact Sheets
        • Personal Stories
        • For health professionals
      • Sport and Exercise
        • On the move with haemophilia
          • Welcome to On the Move with Haemophilia
          • About haemophilia
          • Exercise and haemophilia
          • Exercise and sports
          • Factors to consider
          • Warm ups and cool downs
          • Protection
          • Managing bleeds and injuries
          • Recovery and rehabilitation
          • Tips for parents, teachers, coaches and friends
    • For Health Professionals
      • Nursing
      • Getting Older
      • Hepatitis C
    • National Haemophilia Journal
  • Get Involved
    • Donate Now
    • Fundraising
    • Join HFACT
    • Update my details
    • Volunteer
    • Donate Blood
    • Events
      • Past Events
    • News

National Haemophilia Journal

The National Haemophilia Journal is published by our National Body - please click below to view the Journal.
National Haemophilia Journal


Haemophilia Foundation ACT

Publications

  • Introductory Brochure
  • Newsletter
    • Back Copies
  • Annual Reports
  • Information Resources
    • Bleeding Disorders
    • Haemophilia
      • Newly Diagnosed
      • Haemophilia booklets & fact sheets
      • Mild Haemophilia
      • Living with Mild Haemophilia
      • Haemophilia testing in women and girls - your questions
      • Sport
      • Gene therapy
    • Von Willebrand Disease
    • Women with Bleeding Disorders
      • Young women
      • Haemophilia testing in women and girls - your questions
      • Telling others
      • Sport and exercise for young women
    • Young People
    • Getting older
      • Getting Older Info Hub
      • For health professionals
    • Hepatitis C
      • Hep C Fact Sheets
      • Personal Stories
      • For health professionals
    • Sport and Exercise
      • On the move with haemophilia
        • Welcome to On the Move with Haemophilia
        • About haemophilia
        • Exercise and haemophilia
        • Exercise and sports
        • Factors to consider
        • Warm ups and cool downs
        • Protection
        • Managing bleeds and injuries
        • Recovery and rehabilitation
        • Tips for parents, teachers, coaches and friends
  • For Health Professionals
    • Nursing
    • Getting Older
    • Hepatitis C
  • National Haemophilia Journal

Helpful links

  • Counsellor
  • Treatment in ACT
  • Newsletter
  • Sign up for our eNews
  • Join HFACT
  • Update My Details
  • News
Supported by ACT Health Directorate
ACT Government

HFA NATIONAL

  • T  03 9885 7800
  • 1800 807 173 (toll free)
  • E  [email protected]
  • W www.haemophilia.org.au

STAY CONNECTED

  • HFA Facebook
  • HFA Instagram
  • HFA Twitter
  • HFA YouTube

HFACT

  • E  [email protected]
  • PO Box 331
    MAWSON ACT 2607
  • ABN 39089502414
contact us
Haemophilia Foundation ACT
© 2023 Haemophilia Foundation ACT
Privacy PolicyDisclaimerSite CreditsContact UsSite Map
Registered Charity