Haemophilia Foundation
Australia
Skip to content
Normal contrast
High contrast
MENU
Search for:
Login
donate
Today
Home
About Us
Who We Are
What We Do
Our Advocacy Work
Our Council
Meet the Staff
Our Supporters
Contact Us
About Bleeding Disorders
Latest Information
Fast Facts
FAQs
View All FAQs
Haemophilia
Newly diagnosed with haemophilia
Von Willebrand Disease
Women with Bleeding Disorders
The Female Factors
Self-advocacy for women
Haemophilia and carrying the gene
Haemophilia testing in women and girls
VWD in females
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
World Hepatitis Day
HIV
HIV and Bleeding Disorders
Living with HIV
40 years of HIV - where to next?
Living with a Bleeding Disorder
Personal Stories
HFA YouTube Channel
Newly Diagnosed
Parents and Families
Accessing treatment - Leah's story
Ben – a father’s perspective
Mindi Palm - Living like a Swede
Poppa and Roman share a special bond
Growing up with a bleeding disorder
Youth
Tim - young person with haemophilia
Alan - telling others
Shauna - sharing her life experience living with a bleeding disorder
Stories by Young People
Women
Jane's story - genetic testing for haemophilia
Sharron - A woman with haemophilia, carrier, mother of a son with haemophilia, dad has haemophilia
Susie ~ Disclosure and telling others
Haemophilia - Do You Catch It?
Haemophilia - when your daughters bleed too
Haemophilia - All in the Family
Susie – living with type 1 von Willebrand disorder
Living with haemophilia
Growing Older with Haemophilia ~ Jason
Living with VWD
Living life actively with VWD
VWD – Down the generations
Susie – living with type 1 von Willebrand disorder
Shauna Adams – managing type 3 VWD
Connection & Peer Support
Connecting to others
Overcoming Challenges
Sharing Knowledge
Family & Community Camps
Getting Older
Mike - older person with haemophilia
Hepatitis C
Finally cured of hep C – Alex’s story
Jake's liver health journey
Turning liver health around after hep C – Jake’s story
Clearing hep C as a child - John's story
Finally cured of hep C - Gavin's story
Women can have hep C too - Mary Jane's story
Hep C - I am cured [video]
Anth's treatment story
Simon's treatment story
Len's treatment story
Paul's treatment story
David's treatment story
Share your story
Disclosure
Travel
Travel tips
Getting Older Hub
Safety and Supply
Support & Services
State & Territory Foundations
Treatment Services
Getting Older Hub
Health & Wellbeing
Exercise, arthritis and balance
Bleeding problems
Pain
Mental wellbeing
Surgery and joint replacement
Working with your GP
Personal experiences
Services For Getting Older
Work & Finances
Concession cards
Financial planning and management
Working
Support
Recreation & Travel
Travel tips
Travel stories
Gavin's outback camping story
Zev's travel tips
Your travel story?
Planning For The Future
Connect To Others
Personal experiences
Perry and living with VWD
Mike and getting older
Zev and Mike and staying active
Resilience - David and Zev and Mike
For Health Professionals
International Haemophilia Links
Other Links
ABDR & MyABDR
ABDR
What is MyABDR
Why use MyABDR?
MyABDR Updates
Privacy Consent
Background
Have Your Say
MyABDR Feedback
Youth
Factored In - youth website
Understanding Youth Needs
Youth News
Kids
Colouring in fun!
Livewire
Health Professional Groups
Awards
DCMEF
Publications
News
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
Prophylaxis colouring book
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 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
Ordering HFA print publications
For Health Professionals
Nursing
Getting Older
Hepatitis C
National Haemophilia Journal
Videos & Webinars Library
Bleeding Disorders Awareness Month 2022
Travel Tips Webinar
New Therapies Webinar
Choosing or changing your career path Webinar
Your rights: superannuation and insurance webinar
Conference 2021
Adapting to Change - World Haemophilia Day 2021
Bleeding Disorders Awareness Week 2020
Youtube
Reports & Policy
Young People
Getting Older
Getting Older full report
Hepatitis C
Annual Reports
Promotional Resources
Awareness Newsletters
Research
Research Fund
Research Fund Grants
PROBE study
Getting Older Project
Participating in Research
Clinical Research
Social Research
Market Research
Questions to Ask
Complaints
Events & Conferences
Events
Bleeding Disorders Awareness Month
Resources & Fun Activities
Resource Order Form
Events
Share your story
Donate to support our community
World Haemophilia Day 2023
Organise Your Own Event
Fundraise for Us
Past Events
Conferences
2023 Conference
Presentations
Sponsors
2021 Conference
Presentations
Plenary 1 - The changing world of bleeding disorders
Concurrent 1 - Managing bleeds under current new treatments
Concurrent 2 - Von Willebrand disease
Concurrent 3 - Sex, sexuality and intimacy
Concurrent 4 - Women and girls
Plenary 2 - Dealing with change
Plenary 3 - Pain
Concurrent 5 - Making the most of your health virtually
Concurrent 6 - Getting stronger safely
Concurrent 7 - Youth - challenges, taboos and myths
Concurrent 8 - Getting older
Plenary 4 - Where to from here?
Remembrance Service
Program
Sponsors
2019 Conference
Abstracts & Presentations
Program
Sponsors
2017 Conference
Abstracts & Presentations
Sponsors
Program
2015 Conference
Abstracts and Presentations
2011 Conference
Abstracts and Presentations
2009 Conference
Abstracts and Presentations
2007 Conference
Event Listing
Support Us
Donate
Donate Now
Ways to Give
A Reason to Give
Give Monthly
A Gift in your Will
Give in Celebration
Give in Memory
Fundraise for Us
COVID-19
Tips
Was this page helpful?
About haemophilia in females
Haemophilia symptoms in females
Haemophilia genetic testing
Family Planning
Pregnancy
Tips
References
What tips do others have?
YOU ARE NOT ALONE
Stay in regular contact with your local
Haemophilia Treatment Centre (HTC) team
and make sure you keep up with anything new. The HTC is there to help and can give you advice or talk over any problems or concerns
Keep in touch with your
Haemophilia Foundation
for updates on new information and enjoy a chat with other women who know what it’s like.
IF YOU HAVE A BLEEDING DISORDER
Bring HFA booklets with you to any medical, health or dental appointments
. You can use them to help answer questions you might be asked. Your HTC might also have specific brochures you can take with you, for example, on surgery or dentistry if you have a bleeding disorder.
Make sure you know what type of bleeding disorder you have and how severe it is.
If you are registered for the ABDR, ask the Haemophilia Treatment Centre to organise an ABDR patient card for you.
The ABDR patient card explains your diagnosis, what treatment you should be given and who should be contacted for further advice. Keep the card on you for quick reference.
Show your other doctors, dentist, and health care providers your ABDR patient card and ask them to liaise with your Haemophilia Treatment Centre.
This will help with getting appropriate treatment. It will also make it easier to obtain treatment if you need it when you are away from your usual hospital or Haemophilia Treatment Centre, for example, if you are travelling or have moved interstate or overseas.
Always inform your doctor, dentist or surgeon if you have a bleeding disorder before having any medical, dental or surgical procedures, no matter how minor.
Before you have any procedures, contact your Haemophilia Treatment Centre and discuss the medical support you may need to prevent bleeding complications.
Where possible, plan this well ahead of time. The Haemophilia Treatment Centre team may also need to liaise with your surgical or dental team or other health professionals involved in your care to discuss the best approach for you individually and any pre- or post-treatment care you may need.
Before you start taking anything prescribed by your doctor, naturopath or other health practitioner check with them whether it is safe for someone with a bleeding disorder.
Some medicines, vitamins and supplements can interfere with blood clotting and healing, or can irritate your mucous membranes such as your nasal passages or stomach lining. This includes some herbal and homeopathic medicines and others available over-the-counter, such as aspirin and non-steroidal anti-inflammatory drugs like ibuprofen. Speak with your haematologist or your pharmacist about which medicines you need to be cautious with or avoid.
Date last reviewed: September 2023