I’ve been meaning to write this blog post for a few days now… but it has been a hell of a lot more difficult to start than my previous one in this series (This is my MS – physical symptoms). It was easy for me to write about the physical symptoms of my MS – I am at the stage now where I live with them everyday. No more periods of remission for me, just a constantly ‘dead’ leg, cramps and spasms and fatigue. Luckily, I have found that these can be somewhat controlled, namely through medication and lifestyle factors, which I will write about another day. But I thought that for today, I would focus on the mind – how living with a diagnosis of Multiple Sclerosis (MS) for almost 25 years has impacted upon me; my thoughts and feelings and my attitude to life.
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