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Woman who began coughing up blood was told her 'eyeball could explode' before receiving devastating diagnosis

Home> News> Health

Published 12:07 28 Nov 2024 GMT

Woman who began coughing up blood was told her 'eyeball could explode' before receiving devastating diagnosis

Doctors said her eye was about two weeks from bursting in her head when they removed it

Joe Harker

Joe Harker

A woman became 'one of two in the world' to lose her eye to a rare condition which could have resulted in her eyeball exploding.

Holly Swindells noticed a series of worrying symptoms including her right eye becoming red and painful, while she was also getting nosebleeds and coughing up blood.

With her symptoms getting very worrying she made several trips to see a GP and went to A&E, but they were not able to diagnose what was wrong with her and the pain became so much than she ended up becoming bedbound.

In the end, a blood test revealed she had a rare condition called granulomatosis with polyangiitis (GPA), a rare form of vasculitis, which causes inflammation of blood vessels, including in a person's eyes.

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The Bolton woman, 34, described the pain as being 'like a red hot poker being stabbed through my head constantly' and it reached unbearable levels.

After she was diagnosed doctors told Holly her eye could explode if they didn't remove it. (SWNS)
After she was diagnosed doctors told Holly her eye could explode if they didn't remove it. (SWNS)

Holly, a mum-of-two, eventually had to have her right eye removed after doctors told her that the pressure was so much that her eyeball was in danger of bursting.

Her nosebleeds and coughing up blood were also the result of inflammation from GPA.

With her right eye removed before it could explode, Holly now wears a glittery prosthetic in place of it.

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She said: "I had no idea what GPA vasculitis was - but I was relieved that I finally knew what was wrong.

"By the time I had my eye removed, I had gone blind on that side anyway - I just wanted it out so the pain would stop. I've been having treatments to help with painful inflammation in my joints, but I'm not in remission yet.

"Now I want to raise awareness - a lot of people don't know about GPA vasculitis. I lost my eye but I've come to accept it - and my daughter loves telling everyone about her mummy's glitter eye."

She's now got a glittery prosthetic eye, and says her daughter loves it (SWNS)
She's now got a glittery prosthetic eye, and says her daughter loves it (SWNS)

The 34-year-old first started getting symptoms in December 2021 and was prescribed steroid eye drops by an optician, though they didn't help and by February the following year the pain was in her joints and she was bedbound.

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She said that at the time it 'felt like my body was shutting down from the pain' and things reached the point where she couldn't take her daughter to school or lift up her infant son.

After several trips to visit doctors she called a specialist eye hospital in March 2022 which is where she got a blood test which led to her GPA vasculitis diagnosis.

The inflammation was detected in her ears, nose, sinuses, kidneys, lungs and eyes, and she was admitted to Salford Royal Hospital where she had plasma exchanges through an artery in her neck along with steroids and chemotherapy treatment.

She's had regular treatment since then but she still struggles with symptoms, as Holly said she struggles to walk because of her joints and lungs, and has 'had reoccurrences of my lung haemorrhages too'.

By the time her eye was removed doctors told her she'd been about two weeks away from it popping while still inside her head, and a biopsy had found it was 'fully of inflammatory tumours'.

Featured Image Credit: SWNS

Topics: UK News, Health

Joe Harker
Joe Harker

Joe graduated from the University of Salford with a degree in Journalism and worked for Reach before joining the LADbible Group. When not writing he enjoys the nerdier things in life like painting wargaming miniatures and chatting with other nerds on the internet. He's also spent a few years coaching fencing. Contact him via [email protected]

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@MrJoeHarker

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