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I wanted to know how GH would impact myself and my family, and future generations.

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My sister and I are both in the same practice; one doctor said he would monitor her every 6 months because they’re not sure whether carriers are at no risk. The doctor said to me, ‘you’re just a carrier, it’ll be no problem for you or your children.’

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My mother had on her death certificate, ischemic heart disease. It could have all been because they didn’t know; they didn’t test for haemochromatosis.

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I now feel pretty clued in about it and the way it can impact your life.

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