Louise Chapman with two of her three beloved labradors Walking along a sunny, cobbled street in Mallorca, eating ice creams alongside my husband and daughter, my phone rang. It was my GP. ‘The results of your MRI scans are back in,’ she said, ‘and I have to say, Lou, it is looking like MS’. I stopped in shock. All I could say was, ‘Oh. Oh.’ Then I asked her: ‘And… what exactly is MS?’. Back at the hotel, I started Googling – and I was terrified. MS is incurable.
MS nurses are amazing; if I have to leave a message, they always call back and, depending on your issue, they can speak directly to neurologists and refer patients accordingly. They are very kind and caring, and I feel very lucky to have access to their help in my area. Charities like the MS Trust are also incredibly helpful. You’re not alone. That’s not to say it’s been easy.
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