Hannah has wheels. Hannah has a horn. Hannah has front and rear suspension, and she is coming for you at 4 mph. I wouldn’t say that the purchase of my mobility scooter has been 7 years in the making, far from it, but definitely the last 2 or so. The absolute reluctance of owning... Continue Reading →
Almost 7 years diagnosed and numerous ‘minor’ relapses (I say minor in that I can still function with my life for the best part with a few adjustments and taking a step back for a week or so to recover (to a extent)), Rebif injections, Tysabri infusions, 2 rounds of Lemtrada, more steroid orals and... Continue Reading →
So, many people see and hear the effects Multiple Sclerosis has on me, but why? What is causing me to drag my feet? Go dizzy? Constant pins and needles?Numbness/Paralysis? Fatigue? Double vision, to name but a few? To understand MS, it helps to understand how the central nervous system works. MS is believed to be... Continue Reading →
It was like being diagnosed all.over.again. Early March this year there I was again, hobbling into neurology, for what had started to become a monthly visit for one reason or another. Only now, I was heavily reliant on 2 crutches, in the space of a year I had gone from nothing, to a walking to... Continue Reading →
Hannah Clayson. 26. Diagnosed with Relapsing Remitting Multiple Sclerosis February 2013. Current treatment – Tysabri (Natalizumab) Past treatment - Rebif I am now in the limbo stage between Rapidly Evolving Severe Relapsing Remitting and Relapsing Secondary Progressive MS. Only time will tell. It’s all MS. Everyday I’m shuffling, regardless. From this day onwards, everything made... Continue Reading →
Wednesday February 13th 2013 . The day before my 25th birthday. 'You have Multiple Sclerosis'. Happy Birthday. The relapse which led to my diagnosis started mid November 2012, I used to start work at 6am, so by the time I got home at 2.30 a nap was needed, makes perfect sense doesn't it?! Now, I... Continue Reading →
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