A woman has revealed she has been diagnosed with a rare condition that causes ‘imitation strokes’. She hopes to raise awareness of her condition, sharing that she fears it could leave her wheelchair-bound for life.
Leona Hargreaves, 26, was going about her day at work in October 2024 when she suddenly experienced a weakened left side, lost the ability to speak, and suffered vision loss in her left eye. Her husband Sam, also 26 and an aircraft technician, took her to Lincoln County Hospital where she was diagnosed with hemiplegic migraines following blood tests and a CT scan.
The condition affects one in 10,000 people and mimics stroke symptoms such as slurred speech, muscle weakness, and confusion. Sadly, there us no cure.
Leona Hargreaves suffers with hemiplegic migraines
(Image: © Leona Hargreaves© SWNS)
Leona, who is already dependent on a mobility aid during and after attacks, expressed her fear of experiencing a migraine so severe that she might never walk again. The dental nurse from Lincoln shared: “Hemiplegic migraines have had such a big impact on my life – I’m so scared they’ll damage me permanently.”
She added: “Every attack I have, I wonder if it’ll be the one to leave me permanently unable to walk.”
The condition significantly affected her independence, limiting her ability to work full-time and socialise. Leona said there are many misconception about migraines.
She explains: “People think migraines of any kind last a day, and then when the headache’s gone, it’s gone.” She explained the ordeal of feeling the build-up for days, enduring the migraine itself, and then dealing with the aftermath, which can last up to a week.
Leona Hargreaves was randomly struck with a weakened left side and vision loss in her left eye in October 2024
(Image: © Leona Hargreaves© SWNS)
When Leona was around the age of 13, she started to have migraines and blurred vision which continued until she was 16. It was at this age her painful migraines stopped, gifting her ten years of respite.
“I had migraines regularly for about three years,” Leona recounted. “Then, at 16, they just stopped happening. I had a decade of being migraine-free.”
Having been rushed to Lincoln County Hospital, she recalled: “Everyone thought I’d had a stroke. I remember having sheer panic, thinking: ‘Oh my god, I’m going to die.’”
Despite numerous tests indicating normal results, Leona was eventually diagnosed. She shared, “I had CT scans, an MRI and blood tests – but everything came back normal. At the end of it, I was diagnosed with hemiplegic migraines – and told they’d call me back in to tell me about treatment.”
Not willing to wait any longer, she reached out for faster treatment at the National Migraine Centre in St John’s Wood, London, as debilitating attacks continue to afflict her every few weeks.
Leona says her rare migraines may leave her needing a wheelchair permanently – and she has an imitation stroke every two weeks
(Image: © Leona Hargreaves© SWNS)
Leona suffers from severe attacks that not only leave her with weakened muscles and mobility problems but also mean she’s had to start using a walking stick for support during and after her intense migraines. At only 26, Leona feels that relying on the walking stick is akin to conceding defeat. She added: “I feel like getting the walking stick means I’ve admitted defeat a little bit.”
“But I guess it does mean I can go out, and not always have to cancel plans.I’ve been trying to work full-time through the migraines, but starting from this month, I’ve had to reduce my hours to three days a week.”
“I was just having so much time off.” The road ahead is uncertain for her, but her treatment might include various options such as anti-epilepsy drugs, botox injections for muscle issues, and Vydura for migraine relief.
Regarding treatment possibilities, Leona is hesitant about certain routes, stating: “I can get botox in my head, which I’m not considering just yet,” and expressing reluctance to take medication if avoidable: “I don’t want to be taking anti-epilepsy medication if I can help it, so I’m starting on Vydura to help my symptoms.”
She remains hopeful about the benefits of Vydura, noting, “You can also take it during the onset of an attack, so I’m hoping it’ll help hugely.”