Sly Saint
Senior Member (Voting Rights)
Living with an unsociable illness
full blog here
http://notjusttired.com/2019/04/18/living-with-an-unsociable-illness/
As I’m writing this post, I’m sat in bed, having to take time out to rest, whilst we have a family member staying with us for the weekend. Enjoying listening from afar to the lively chatter, yet not a part of it. Would I not rather be downstairs, chatting and laughing with everyone?
Of course I would. However, living with ME/CFS, means that I’m also living with an unsociable illness. Not through choice of course, but due to the nature of the illness and it’s debilitating symptoms.
It can be really hard to explain this to people. The physical impacts of living with ME/CFS can often be easier to get your head around. Whereas the cognitive issues are not so easy to understand, and of course not easy to deal with.
Debilitating brain fog, struggling to follow a conversation, noise sensitivity, the exhaustion that comes from merely speaking to someone, are frustrating to say the least. Who knew (until living with ME of course!) these things could use up so much energy! As well as causing pain, a flare up of symptoms, sometimes embarrassment, and for many loneliness. As we are forced to withdraw from social situations.
full blog here
http://notjusttired.com/2019/04/18/living-with-an-unsociable-illness/