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Karen Bellerby, a 62-year-old woman from Marks Tey in Colchester, shared her experience of being diagnosed with multiple sclerosis (MS) in 2019. Her life took a drastic turn when she received the news.

Before the diagnosis, Karen’s job involved a lot of public speaking. Her first symptom was a fear of slurring her words. She described a bizarre feeling that she was slurring when she spoke. This was particularly concerning for her as a regular public speaker. Although her family reassured her that she sounded fine, the feeling was unsettling and prompted her to seek medical help.

Upon receiving the diagnosis of MS, Karen and her family were shocked and surprised. She didn’t feel ill at the time, which made the news even more difficult to process. MS is an unpredictable disease that occurs when the immune system attacks the protective coating around nerve fibres in the brain and spinal cord. Symptoms can vary and may include mobility issues, cognitive problems, extreme fatigue, and vision impairments.

Karen has relapsing-remitting MS, the most common type, where individuals can go years without symptoms only to experience sudden relapses that may lead to lasting disability. The uncertainty of when the next relapse may occur has been the most challenging aspect for her to accept.

To cope with the unpredictability of the condition, Karen is participating in a fundraising event called The Gherkin Challenge in London to support MS-UK. This event involves climbing the iconic skyscraper to raise money for individuals living with MS. Despite not experiencing severe symptoms currently, Karen’s determination to help others and make the most of her abilities while she can has only grown stronger.

She views the Tower Walk as an opportunity to enjoy the city she loves while contributing to a cause that supports people with MS. Karen’s story exemplifies resilience and the power of community support in facing life’s challenges. Her courage and determination serve as an inspiration to others living with MS and those supporting loved ones with the condition.