Three glasses of water and a pie review? This is the kind of field research we support.
Thanks for the shout-out, Tony. A timely reminder to stay on top of treatment, follow medical advice, and hydrate like a professional. 🥤🥤🥤🥧
#beatoverload#WHW2026
Our co-patron and long-serving medical advisor, Professor John Olynyk, has been awarded a Member of the Order of Australia, AM, in the King’s Birthday Honours List.
We also acknowledge the late Professor Katie Allen AO, also recognised in today’s King’s Birthday Honours.
National Blood Donor Week starts today.
This June Action Month, we are encouraging our community to take practical action.
Already a donor? Join the Haemochromatosis Australia Lifeblood Team. If not sure whether you can donate, talk to your GP. https://t.co/UI4VaU36FO
Donate if you can. Share if you can’t.
This June, take action in the way that is right for you. Join the HA Lifeblood Team, share the message, or encourage one person to learn more about haemochromatosis.
https://t.co/c5YgQll72O
#WHW2026#beatoverload
Help Haemochromatosis Australia reach 2,000 Registry participants!
If you are 18+ with a confirmed diagnosis, your experience can help improve understanding of diagnosis, treatment access, health outcomes and lived experience.
https://t.co/kIPDHScyrf
#WHW2026
When Sam was diagnosed with haemochromatosis, he wanted clear information and support.
His GP suggested Haemochromatosis Australia. Within 48 hours, Sam received a response that helped him feel reassured and better informed.
https://t.co/c5YgQll72O
#WHW2026#beatoverload
Are you the first in your family to be diagnosed?
Haemochromatosis runs in families. Your diagnosis may be important information for close biological relatives.
Use HA’s Family Letter to help start the conversation.
https://t.co/c5YgQll72O
#WHW2026#beatoverload
Are you the first in your family to be diagnosed?
Haemochromatosis runs in families. Your diagnosis may be important information for close biological relatives.
Use HA’s Family Letter to help start the conversation.
https://t.co/vVU295mEdB
#WHW2026#beatoverload
World Haemochromatosis Week starts today.
This June, move from awareness to action:
Talk to your family.
Speak with your GP.
Use HA’s resources.
Join the Registry if eligible.
Donate blood if you can.
Share the message.
https://t.co/c5YgQll72O
#WHW2026#beatoverload
World Haemochromatosis Week starts tomorrow.
This June, take action in the way that is right for you:
1. Talk to your family
2. Speak to your GP
3. Join the Registry if eligible
4. Donate blood if you can
5. Share your story
6. Share the message
https://t.co/xfws0ZlJfo
You are not alone.
If you or someone in your family is affected by haemochromatosis, Haemochromatosis Australia provides information, resources and support.
Call the HA Info Line on 1300 019 028 or visit https://t.co/TinW5nupfj
#WHW2026#beatoverload
Help us reach 2,000 Registry participants!
If 18+ with a confirmed diagnosis of haemochromatosis, you can help improve understanding of diagnosis, treatment access, health outcomes and patient experience.
Join the Australian Haemochromatosis Registry: https://t.co/TinW5nupfj
If haemochromatosis is in your family, our Family Letter can help you start an informed conversation with your GP.
It is part of our From Awareness to Action Toolkit we will highlight during World Haemochromatosis Week from 1 June. https://t.co/xfws0ZlJfo
#WHW2026#beatoverload
Haemochromatosis runs in families.
If diagnosed one of the most useful things to do is encourage close biological relatives to speak with their GP.
Our Family Letter can help start the conversation.
Find the letter: https://t.co/xfws0ZlJfo
#WHW2026#beatoverload
Haemochromatosis causes the body to absorb and store too much iron, and can lead to serious health problems if not diagnosed and managed.
In June, we’re helping more Australians learn what to ask, where to get support and how to take the next step. https://t.co/xfws0ZlJfo
World Haemochromatosis Week is coming: 1–7 June 2026.
This year, Haemochromatosis Australia wants to help more people move from awareness to action, with a month-long campaign planned for June.
Visit the campaign page: https://t.co/vVU295mEdB
#WHW2026#beatoverload
It's National Volunteer Week! Haemochromatosis Australia could not function without our volunteers. In fact, we are all volunteers. Thank you to all our wonderful volunteers. If you would like to help visit https://t.co/2Is1McZytR #NVW2026#haemochromatosis#ironoverload
Jeff and Tony are representing #Haemochromatosis Australia at the 2026 Aust Rheumatology Association ASM on the Gold Coast 16–19 May. Attending? Visit us at Stand 6 for patient resources & info on the Australian Haemochromatosis Registry. https://t.co/c5YgQll72O #ARA2026
Matthew shares how he discovered he had haemochromatosis—what’s your story?
We’d love to hear about your journey, thoughts or how it impacts your life. Share your story in 'Iron Age News' & help others feel less alone.
https://t.co/sk7Fp8tOl4
#haemochromatosis#ironoverload
Many thanks to Judi for her continued support raising awareness of #haemochromatosis https://t.co/HiiQzMBbo6 https://t.co/0OdPSup5AH
#ironoverload#WHW2026