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
      • Other women's resources
    • 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
      • HFA hepatitis C strategy
      • Double Whammy Report
      • Getting It Right evaluation
      • Hep C Resources
      • Hep C Treatments
      • Telling others about hep C
    • HIV
      • HIV and Bleeding Disorders
      • Living with HIV
    • Travel
    • Disclosure
    • ABDR
    • MyABDR
      • What is MyABDR
      • Why use MyABDR?
      • MyABDR Updates
      • Privacy Consent
      • Background
      • Have Your Say
      • MyABDR Feedback
    • Safety and Supply
    • Personal Stories
      • Women
      • Hepatitis C
        • Anth's treatment story 2018
        • Simon's treatment story 2017
        • Len's treatment story 2017
        • Paul's treatment story 2017
        • David's treatment story 2016
      • Youth
      • Newly Diagnosed
      • Living with haemophilia
      • Living with VWD
      • Growing up with a bleeding disorder
  • Support & Services
    • Foundation Services
    • Support Groups
    • Member Benefits
    • Our Counsellor
    • Community Camp
    • Government Support
    • Community Organisations
    • 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
    • Bleeding Disorders
    • Introductory Brochure
    • Newsletter
      • Back Copies
    • Annual Reports
    • Haemophilia
      • Newly Diagnosed
      • Haemophilia Resources
      • Mild Haemophilia
      • Living with Mild Haemophilia
      • Sport
      • Gene therapy
    • Von Willebrand Disease
    • Women with Bleeding Disorders
      • Young women
      • Telling others
    • Hepatitis C
      • Hep C Fact Sheets
      • Personal Stories
      • Reports
      • For health professionals
    • Getting older
      • For health professionals
    • Young People
    • Nursing
    • National Haemophilia Journal
  • Get Involved
    • Donate Now
    • Fundraising
    • Join HFACT
    • Update my details
    • HFACT Calendar
    • Volunteer
    • Donate Blood
    • Events
      • Past Events
    • News

Youth

There are loads of things to look at here. Join the youth community through Factored In, read about the Youth Lead Connect program or check out the colouring in pages below.


Youth News
Factored In - youth website
Colouring in fun!

Haemophilia Foundation ACT

Support & Services

  • Foundation Services
  • Support Groups
  • Member Benefits
  • Our Counsellor
  • Community Camp
  • Government Support
  • Community Organisations
  • 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

Helpful links

  • Calendar
  • Counsellor
  • Treatment in ACT
  • Newsletter
  • 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
© 2021 Haemophilia Foundation ACT
Privacy PolicyDisclaimerSite CreditsContact UsSite Map
Registered Charity