Haemophilia Foundation New South Wales

Skip to content Normal contrast High contrast
Menu
MENU
Contact Us Donate
  • Home
    • News
  • About Us
    • Who We Are
    • Our Committee & Staff
    • 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
    • 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
    • HFNSW Family Camp
    • State & Territory Foundations
    • Treatment Services
    • Kids
      • Colouring in fun!
      • Livewire
    • Youth
      • Factored In - youth website
      • Youth News
      • Livewire
      • Colouring in fun!
  • Publications
    • Bleeding Disorders
    • Factor Matters Newsletter
    • 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
      • Getting Older with a Bleeding Disorder: Needs Assessment Report
    • Young People
    • Nursing
    • National Haemophilia Journal
  • Get Involved
    • Donate Now
    • Fundraising
    • Memberships
      • Members Contact Details Updates Form
    • Volunteer
    • Events
      • Past Events
    • News
    • Share Your Story
    • Surveys
      • Annual Family Camp Survey
      • HFNSW Events Survey

Living with Mild Haemophilia

Living with mild haemophilia: a guide - October 2011

A comprehensive guide to living with mild haemophilia, including diagnosis, genetic inheritance and planning a family, treatment and care, special issues for girls and women and information on living well.

Download Full Booklet 2.95MB

SECTIONS

Understanding mild haemophilia 407KB
How bleeding starts and stops 159KB
Diagnosis 511KB
Family and inheritance 121KB
Treatment and care (includes what to do about an injury or bleeding) 289KB
Living with mild haemophilia (Travel, sport, work, school, telling others, support) 986KB
Carrying the haemophilia gene (Special issues for girls and women) 788KB
Planning a family 111KB
Living well with mild haemophilia 311KB
More information 411KB
 


Haemophilia Foundation NSW

Publications

  • Bleeding Disorders
  • Factor Matters Newsletter
  • 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
    • Getting Older with a Bleeding Disorder: Needs Assessment Report
  • Young People
  • Nursing
  • 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

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

HFNSW

  • T  02 9280 2607
  • E  [email protected]
  • Suite 5, 88 Mountain Street, 
    Ultimo NSW 2007
contact us
Haemophilia Foundation NSW
© 2021 Haemophilia Foundation New South Wales
Privacy PolicyDisclaimerSite CreditsContact UsSite Map