Here comes the sun…

Ahhh the British summertime is a funny one, isn’t it? Full on melt downs (sun or otherwise with the current pandemic at the moment), gale force winds, and rain all in the space of a week. However, when the sun is out this is when I am at my optimum level and many of my... Continue Reading →

On the road again…

I absolutely love travelling, seeing the world, experiencing and learning from different people and cultures. It’s a passion that I hold dear to my heart, and I aim to visit all 195 countries before I join the gig in the sky. However, this piece brings me a bit closer to home as I talk about... Continue Reading →

Carers Week 8-14 June 2020

Being a carer comes in many forms. Some individuals wouldn’t even consider themselves a carer. In essence, if you provide support for someone who cannot otherwise cope – you are a carer, irrespective of whether it is ongoing, ad-hoc, or recovery from an injury/illness/addiction etc – it is care. Care that someone is providing for... Continue Reading →

They see me rollin’…

  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 →

Hello darkness my old friend…

13th February 2013 frames the before and after of my life. It’s impossible to get through grief that hasn’t happened yet as MS is a constant moving target. So with that, almost 7 years diagnosed and numerous ‘minor’ relapses (I say minor in that I can still function with my life for the best part... Continue Reading →

What is all of this MS palava?

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 →

Tysabri – Miss Positive(ity)

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 →

MS really gets on my nerves – About Me.

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 →

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