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.
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.