On 7th November 2021, I started to feel constant pins & needles in my feet. The sensation lasted a few days before gradually travelling up my body, eventually stopping at my pelvis. At my worst point, I could hardly walk unaided, and was confined to my bed. It was terrifying not knowing what was wrong with me. After numerous MRI’s, blood tests, neurological tests and nerve tests, I was finally diagnosed with Multiple Sclerosis (MS). It’s a condition that affects many people but every person’s experience is unique as it affects each individual differently. I’m glad to say that, although I’m not 100%, I am doing very well. I have bad days but I keep going and try to stay as positive as I can, but that can be difficult, especially not knowing what the future holds for my mobility. I have started treatment, which I’ll receive every 6 months via an IV. Treatments for MS have improved so much over the years, and this is down to research. But, research costs money, money that the Government/NHS unfortunately do not have.

On 9th September, David and I, along with some good friends who have been there for me through it all, are walking 20KM to raise funds for MS. I know it’s a difficult time, financially, for a lot of people, but any donation would be very much appreciated. This money will be donated to help those amazing people who work tirelessly to find a cure for MS sufferers like myself.

Thank you 🥰🧡