Haemophilia Foundation Tasmania

Skip to content Normal contrast High contrast
Menu
MENU
Contact Us Donate
  • Home
  • About Us
    • Who we are
    • Our Committee
    • 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
      • Haemophilia testing in women and girls
      • 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
      • Inherited platelet function disorders
      • Acquired haemophilia
    • 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
    • Support Groups
    • Youth
      • Factored In - youth website
      • Youth News
      • Livewire
      • Colouring in fun!
    • Kids
      • Colouring in fun!
      • Livewire
    • ABDR & MyABDR
      • ABDR
      • What is MyABDR
      • Why use MyABDR?
      • MyABDR Updates
      • Privacy Consent
      • Background
      • Have Your Say
      • MyABDR Feedback
    • State & Territory Foundations
    • Treatment Services
    • HFT Facebook Group
  • Publications
    • Information Resources
      • Bleeding Disorders
      • Haemophilia
        • Newly Diagnosed
        • Haemophilia booklet
        • Gene therapy
        • Mild Haemophilia fact sheet
        • Living with Mild Haemophilia Guide
        • Simple guide to haemophilia testing in women and girls
        • Comprehensive haemophilia testing in women
        • Acquired haemophilia
        • Sport
      • Von Willebrand Disease
      • Women with Bleeding Disorders
        • Young women
        • Sport and exercise for young women
        • Snapshot of bleeding disorders in females
        • Simple guide to haemophilia testing in women and girls
        • Comprehensive haemophilia testing in women
        • Finding out you carry the gene
        • Telling others
      • Young People
      • Getting older
        • Getting Older Info Hub
        • For health professionals
      • Hepatitis C
        • Hep C Fact Sheets
        • Personal Stories
        • Hepatitis C
        • 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
    • Stuart Cousins Memorial Fund
    • Membership
    • Events
      • Past Events
    • News

Mild Haemophilia fact sheet

Mild haemophilia fact sheet

A fact sheet for people with mild haemophilia, with information about what you need to know about mild haemophilia, symptoms, treatment, when to seek help, what to tell other doctors and dentists, how to recognise serious bleeding, and tips for living well. (2012)
Download PDF 205KB

 

 


Haemophilia Foundation Tasmania

Publications

  • Information Resources
    • Bleeding Disorders
    • Haemophilia
      • Newly Diagnosed
      • Haemophilia booklet
      • Gene therapy
      • Mild Haemophilia fact sheet
      • Living with Mild Haemophilia Guide
      • Simple guide to haemophilia testing in women and girls
      • Comprehensive haemophilia testing in women
      • Acquired haemophilia
      • Sport
    • Von Willebrand Disease
    • Women with Bleeding Disorders
      • Young women
      • Sport and exercise for young women
      • Snapshot of bleeding disorders in females
      • Simple guide to haemophilia testing in women and girls
      • Comprehensive haemophilia testing in women
      • Finding out you carry the gene
      • Telling others
    • Young People
    • Getting older
      • Getting Older Info Hub
      • For health professionals
    • Hepatitis C
      • Hep C Fact Sheets
      • Personal Stories
      • Hepatitis C
      • 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

  • Get Involved

HFA NATIONAL

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

STAY CONNECTED

  • HFT Facebook
  • HFA Instagram
  • HFA Twitter
  • HFA Youtube

HFT

  • T  0431 344 575
  • E  [email protected]
  • PO Box 184 Sandy Bay
    TAS 7006 Australia
contact us
Haemophilia Foundation Tasmania
© 2023 Haemophilia Foundation Tasmania
DisclaimerPrivacy PolicySite CreditsContact UsSite Map