Haemophilia Foundation Victoria

Skip to content Normal contrast High contrast
Menu
MENU
Contact Us Donate
  • Home
  • About Us
    • Who We Are
      • Our Mission
      • History
    • What We Do
    • Our Committee & Staff
    • Strategic Plan
    • 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
    • Support Groups
      • Mens Group
      • Womens Group
      • Youth Group
      • Dads Group
      • Grandparents & Friends Group
      • Boys Group
      • Useful Contacts & Other Links
      • Treatment Services
    • Services
    • State & Territory Foundations
    • Treatment Services
    • Youth
      • Factored In - youth website
      • Youth News
      • Livewire
      • Colouring in fun!
    • Kids
      • Colouring in fun!
      • Livewire
  • Publications
    • The Missing Factor Magazine
    • Local resources & publications
      • Alfred HTC Question and Answer Resources
    • Bleeding Disorders
    • 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
    • Annual Reports
    • National Haemophilia Journal
  • Get Involved
    • Donations
    • Fundraising
    • Events
      • Recent Events
    • News
    • Volunteer
    • Memberships
      • Become a Member Today
      • Membership Renewal Form

Youth


Important Note: This information was developed by Haemophilia Foundation Australia for education and information purposes only and does not replace advice from a treating health professional. Always see your health care provider for assessment and advice about your individual health before taking action or relying on published information.
This information may be printed or photocopied for educational purposes.
Haemophilia Foundation Victoria

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

Helpful links

  • Events
  • Get Involved
  • Update my details
Proud Partner of Better Health Channel.

HFA NATIONAL

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

STAY CONNECTED

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

HFV

  • T  03 9555 7595
  • E  [email protected]
  • 13 Keith Street, Hampton East,
    VIC 3188, Australia
contact us
Haemophilia Foundation Victoria
© 2021 Haemophilia Foundation Victoria
Privacy PolicyDisclaimerSite CreditsContact UsSite Map