Connect with us

Health

Genetic Screening for Haemochromatosis Offered in Northern Ireland

Editorial

Published

on

A new initiative has been launched to provide free genetic screening for haemochromatosis, a condition characterized by excessive iron absorption due to genetic factors. This screening aims to raise awareness and promote early detection of the disease, which can lead to serious health complications if left untreated. The initiative is supported by Hagan Homes and other funders, enabling Haemochromatosis UK to cover the £129 cost of testing for participants.

Haemochromatosis can lead to chronic fatigue, joint pain, liver disease, diabetes, and other serious conditions. In many cases, individuals may exhibit no symptoms until significant damage has already occurred. Research by Haemochromatosis UK indicates that approximately one in ten people in Northern Ireland carry the genetic predisposition for this condition.

Community Engagement and Support

The campaign will target households in specific postcodes, providing them with information about genetic haemochromatosis and offering free genetic tests. Alongside testing, participants will have access to genetic counselling to better understand their results. James Hagan, founder of Hagan Homes, shared his personal connection to the cause, stating, “Someone very close to me was recently diagnosed with genetic haemochromatosis—despite having no symptoms. Their experience highlights exactly why this campaign is so important.”

Hagan emphasized the potential seriousness of the condition, noting that most affected individuals do not exhibit warning signs. His commitment to supporting the community underscores the importance of raising awareness about haemochromatosis and its implications.

Jenny Irvine, CEO of the ARC Healthy Living Centre in Irvinestown, expressed enthusiasm for the partnership with Haemochromatosis UK. “ARC staff and directors are delighted to be working with Haemochromatosis UK to encourage people in the Irvinestown area to avail of free screening. This is a wonderful opportunity to raise awareness about what is a very prevalent but under-diagnosed genetic condition,” she said.

Upcoming Events and Awareness Campaigns

As part of the broader awareness campaign, Haemochromatosis UK will present a touring photographic exhibition titled We are Overloaded at Millennium Court in Portadown starting on January 19, 2026. Local volunteer Finbar Polin, who is featured in the exhibition, shared his personal journey with the condition. He noted, “It’s scary because it affects you mentally; you don’t know where you are going with it… the next thing I knew I was diagnosed with diabetes.”

Polin highlighted the lack of awareness among some healthcare professionals regarding haemochromatosis, prompting his involvement with the charity. “I got involved with the charity; it’s good to know there are people to talk to,” he added.

This initiative represents a significant step toward addressing the challenges posed by haemochromatosis in Northern Ireland. By providing free genetic testing and fostering community awareness, stakeholders hope to facilitate early detection and improve health outcomes for those at risk.

Our Editorial team doesn’t just report the news—we live it. Backed by years of frontline experience, we hunt down the facts, verify them to the letter, and deliver the stories that shape our world. Fueled by integrity and a keen eye for nuance, we tackle politics, culture, and technology with incisive analysis. When the headlines change by the minute, you can count on us to cut through the noise and serve you clarity on a silver platter.

Continue Reading

Trending

Copyright © All rights reserved. This website offers general news and educational content for informational purposes only. While we strive for accuracy, we do not guarantee the completeness or reliability of the information provided. The content should not be considered professional advice of any kind. Readers are encouraged to verify facts and consult relevant experts when necessary. We are not responsible for any loss or inconvenience resulting from the use of the information on this site.