When Megan Quinn awakened one morning a few years in the past she knew one thing wasn’t fairly proper.
The then 23-year-old was experiencing dizziness and double vision, whereas her boyfriend observed that her face was drooping to 1 aspect.
She instantly dialled 111 the place name handlers urged her to go to A&E fearing she had suffered a stroke.
Although checks revealed that Megan, from Cumbernauld close to Glasgow, had not suffered a stroke the true reason behind the signs was not decided and she or he was despatched dwelling.
But her signs worsened and after months of going backwards and forwards between medical doctors and the hospital she was hit with a shock prognosis.
Speaking to Glasgow Live, Megan recalled: "I awakened in the future and I used to be actually dizzy. My boyfriend instructed me that my face had drooped to the aspect.
“I had double vision, I had never experienced anything like it before.
"I phoned the doctors but it was a bank holiday so no one picked up. I ended up phoning 111 and they told me to go to A&E because it sounded like a stroke. I was 23 at this point and I was terrified.
"They did a lot of tests in hospital and they were happy to send me home because they didn't think it was a stroke. The symptoms started to get worse."
Just before Christmas last year it was confirmed that accounts assistant Megan had multiple sclerosis - or MS.
“I was back and forth to the eye doctor with double vision and then they sent me for an MRI scan because they couldn't understand what was wrong,” Megan mentioned.
“I met with a neurologist in February 2022 and I used to be instructed that I could have MS.
"I thought the worst. I went for a lumbar puncture in March and then received a scan six months later. In December I was officially diagnosed."
MS is a critical lifelong situation that may have an effect on the mind and spinal wire, resulting in a variety of signs similar to issues with imaginative and prescient, arm or leg motion, sensation or stability.
Average life expectancy is barely decreased for individuals with MS.
Despite this Megan mentioned she feels lucky to be identified at a younger age. She mentioned: "It was horrible. I think I Googled every possibility, which is the worst thing you can do.
“Since we were still in the pandemic it was difficult to pick up the phone and ask what was happening. I assumed that I was going to end up in a wheelchair.
"But I met with my neurologist and he instructed me I'd be enjoyable. I'm fortunate I used to be identified so younger as a result of there may be medicine to assist me and sluggish the speed it progresses at."
Megan is now targeted on elevating consciousness of the situation, together with by participating in a charity stroll in help of the Multiple Sclerosis Society in September. To donate go to her Just Giving web page here.
She added: "There shall be individuals on the market who're my age which were identified. It may be fairly exhausting to speak about in the event you aren't aware of individuals in your age group who even have MS.
"I want to raise awareness of how it affects younger people and raise as much cash as possible so it can be researched. I hope one day there will be a cure."
According to the NHS, the principle signs of MS embrace:
If you expertise signs communicate to your GP.
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