I was 25 when suddenly I lost sensation and strength in my legs on a work trip. After one month in hospital I was diagnosed with Multiple Sclerosis (MS). I had very little understanding of what this meant, but like most of my family and friends, I pictured wheelchairs and a terrifying future. My doctor took very little time to explain what this entailed, so I left hospital not knowing much about my condition, or if indeed I would ever walk properly again. I learnt through my own research that MS is a neurological condition that affects the protective Myelin sheath surrounding the nerves. When this is damaged (by the immune system) it can lead to sensory, cognitive and mobility problems. It is the most common reason for disability in young adults.

After much research, and the help and support from my amazing family and friends I learnt that MS doesn’t necessarily mean wheelchairs, and isn’t something to be frightened of. It is something which people generally know very little about, yet most people I talk to know someone affected by the disease. MS research work to raise people’s awareness and perception of MS, whilst tirelessly working alongside others to find the best possible treatment.... and maybe one day a cure!! Through them I learnt of the medication I am on now, which after 8 relapses in my 1st year, has kept me relapse free for 2 so far. There is little support provided for people who are facing this uncertain and quite frankly terrifying future, so my aim is to help take the stigma out of MS, and get support behind finding a cure for this very common, yet misunderstood disease. Kilimanjaro (at 5,895m or 19,341ft) for me is a massive challenge personally, both mentally and physically. Any donation will make a huge difference, and please don't underestimate how much your support means to me.

Thank you in advance for all your donations and support.

Love Holly xx