Dervla
"I'm a good example of catching it young, starting treatment, and not waiting until it’s taken an irreversible toll on your body."

Dervla did not experience any symptoms, but had her genes sequenced after her son was part of a genetic study for epilepsy. Dervla and her brother, Cormac, took part in the project to demonstrate the importance of early diagnosis of genetic haemochromatosis.

Watch Dervla's story


Of five of us siblings, three had haemochromatosis

My son started having seizures when he was a toddler, and as part of that he was put in a genetic study for the type of epilepsy he has. It was a blind study, but I knew that I was going to want to know if he had the gene.

So, my husband and I thought to get our genes sequenced, and it came back that I had the gene for haemochromatosis.

My brother, Cormac, and my sister have it, so of five of us, three had haemochromatosis. We found out pretty young and weren’t experiencing symptoms; we probably wouldn’t have known for years. 

The biggest thing that would concern me is arthritis. If I keep giving blood, I’ll be well, but I could get arthritis pretty early. When you’re active, you know the kind of toll that would take. 

We're a good example of catching it young, starting treatment, and not waiting until it’s taken an irreversible toll on your body.

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