Living with MS has made one thing unavoidable: life does not stabilise.
There are days when my body feels generous. There are days when it feels unpredictable. Energy rises and falls. Plans chan... Read More
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Hello and welcome to our unique blog post, brought to you by some dedicated members of our employee-led 'Take a Break' committee. This space is specially crafted for our colleagues who find t... Read More
Living with a chronic illness is undeniably challenging. There’s no sugar-coating it. For me, Secondary Progressive Multiple Sclerosis (SPMS) and mobility issues are daily realities. There&rsqu... Read More
Introduction
As someone living with progressive Multiple Sclerosis (MS), I've faced numerous challenges. But through it all, I've learned invaluable lessons, many of which I owe to my la... Read More
I want to tackle a question I get a lot, particularly with my somewhat unorthodox commute– it's the big "why?" Why, with secondary progressive MS and my limited mobility, do I sti... Read More
The older I’ve become and the more this disease progresses, the more I realise that everyone is dealing with something. My average day is not the same as anyone else’s but it is mine.
... Read More
I have MS, it doesn’t have me. I am a full time cityworker, wife and mother of two daughters (12 and 10). I was diagnosed with MS in 2019 but the doctors think I’ve had it since my early ... Read More



