In the spirit of World Haemochromatosis Awareness Week 2024, we are organising a Diet & Haemochromatosis webinar via zoom on Wednesday 19th June @ 7pm, which will be followed by a Q&A session. There will be lots of opportunities for questions. Join us with leading Dietician and Nutritionist, Sarah Keogh www.eatwell.ie and register today. We would love to see you all at this event! You can register here – https://us02web.zoom.us/…/tZMtcOqurzIrEtRnupu3DvQlU5TW6…
For more information or for any queries or questions, email us at [email protected]
Ann Teehan shared her story ‘The Celtic Gene’ of her haemochromatosis journey with readers of ‘Woman’s Way’ magazine last year. Ann and her family are passionate about raising awareness of haemochromatosis, Ireland’s most common genetic disorder. Thank you Ann for sharing your personal journey with us! Read on for link to pdf of full article
As we step into 2025, we’re filled with gratitude for your continued support and commitment to raising awareness about haemochromatosis. Together, we’ve made strides in educating and supporting those affected by iron overload, and we look forward to continuing this important work in the year ahead. May the new year bring all our haemochromatosis family health, happiness, and many moments of joy.
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!
