There is still time to donate to our Christmas Jumper Campaign this year! Miriam is raising funds to support our ongoing work and projects, including our Helpline which supports patients and their families, our information resources for nurses, GPs and healthcare staff and our vital research work. Thank you to everyone who has supported Miriam’s fundraising page so far. We know that people are called on to support many causes in the lead up to Christmas, but if you are able to make any donation big or small, we would be very grateful for your help. Thank you! This donation page will close at the end of January 2024. For donations: https://www.idonate.ie/fundraiser/MiriamFordeIrishHaemochromatosis?fbclid=IwAR2adW6ycAqQREQ72rmCeIL08JPt6C7Gp3CE8MacvTy-U91tyKR9x7aA_6w
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!
