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Many MS Symptoms Are Invisible: We Need to Share Our Stories
In her case a lot of her symptoms are invisible. It’s tough explaining fatigue to someone when you still can walk.
I remember in the early stages of my MS being at work as a TV Casting Director. Normally at the end of the casting we’d all stand – maybe shake the actor’s hand. I had to sit through all of it. It looked rude. Pretty sure at this point I hadn’t ‘outed’ myself!
It was all so new but fatigue had already made its presence felt. Think had already fallen over on the way to the venue!
Do you agree with Jessie that we need to educate others to our disease?
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