Our 2024 education and awareness campaign was launched in April and the campaign’s fun and
engaging approach has successfully informed the public about haemochromatosis, how to recognise
the symptoms, how to get tested and treated and how to manage haemochromatosis. We continue to receive very positive feedback from our members, the public and the medical and health sector on the campaign. Our information and educational messages are simple and easy to understand. Thanks to our collaboration with Harris PR, we have developed a monthly series of digital paid and organic posts across our charity social media platforms. Let us know what you think! If you would like to send us any feedback on the social media campaign, just email [email protected]
We have delivered:
Your membership of the IHA makes us stronger and gives us a collective voice to advocate on behalf of our members, patients and their families. At this time of year, we encourage all our members to renew your annual membership and continue to be part of our 1,000 strong community!
Wear your Christmas jumper to support the work of the Irish Haemochromatosis Association OR make a gift of a donation big or small this holiday season to ensure that patients in Ireland get the help and support they need.
Thank you to all the Donegal community who came out in great numbers to attend our recent Patient Information evening in the Clanree Hotel in Letterkenny, Co Donegal. Over 120 people, some who travelled long distances, joined us on the night to hear Dr. Paul Grant’s talk and presentation on haemochromatosis.
