Wear your Christmas Jumper OR make a donation to support our work

Christmas Jumper Day is back! We are asking you to wear you jumper and raise funds and awareness of haemochromatosis with your friends, in your workplace or at home anytime during the month of December. Although National Christmas Jumper day falls on the 12th December, you can choose any date that suits you right up until the 31st December! Visit: www.idonate.ie/event/ihachristmasjumper2024 and just click ‘Start Fundraising’ to set up a personal page for the IHA. You can also share your page among friends and family.

Wear your best or worst Christmas Jumper and help raise vital funds for our work. Whether you are at home, in your workplace or club gather your friends, family or work colleagues together to get into the festive spirit!

Or you might like to make a donation to support our work. All donations big or small will help support our helpline work, deliver more patient events and distribute more education and information packs to patients and medical professionals.

You can also ask your company to support us by making a Christmas donation to our work – Donate Here: https://haemochromatosis.ie/donate-to-the-iha or email [email protected] for more information.

IHA News and Events

Ann Teehan talks to ‘Woman’s Way’ magazine

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

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Happy New Year for 2025!

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.

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Renewing your Membership of our Haemochromatosis Community!

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!

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