Abigail
'I just kept screaming over and over again...'

Abigail was diagnosed with genetic haemochromatosis aged 15 after suffering from poor mental health. Abigail reflects on the dismissal she experienced by clinicians who assumed that being a young woman meant she was unaffected by the condition.

Watch Abigail's story


Everything I do feels like I'm wading through really thick mud.

When I was a teenager, I suffered with poor mental health, and I was self-harming. I was seen by CAMHS, the Children and Adolescent Mental Health Service, and it was a psychiatrist there who asked me about health conditions that were in my family.

She found that my ferritin was way over what it should have been, and she told me I had something called haemochromatosis. I was just 14 years old.

I was so young and didn’t really know how to speak for myself. The hematologists were telling me, ‘I’m sure things aren’t so bad for you, you’re young.’ I just kept screaming over and over again, that’s not the case; I feel like I can’t get up for school. I’d come out of appointments almost in tears because nobody was taking me seriously.

Everything I do feels like I’m wading through really thick mud. It's sore, it’s heavy, it’s hard. It can be quite dark at times, because I look at people my age doing things that I would love to be doing.  

I’ve always said that this is not an old person’s condition; I am proof in front of you that it’s not.  

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