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A Small World

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Right now I feel as though my world consists of 2 rooms upstairs in my home – ie. my bedroom and my office (which is in the next bedroom). And my day to day life is just : work – exhausted/CFS worse – then sleep.
Then more of the same.
But at least I do have the luxury of working from home and for myself. Which is just as well as some days I work very badly or slowly. And some days I don’t manage at all. But thats nothing unusual with CFS – it just wouldn’t be much good to an employer !
The biggest problem I have right now is when I try to have a decent break to allow my CFS to get a bit better – all the work problems escalate. (I always have a backlog as its hard to get on top of things.)  After a few days off I will feel rested and stronger – but then have to face problems that have resulted from me missing things that maybe had to be done by a certain time. And with it being property – almost everything has a financial penalty or cost of some sort. This then causes more work and problems . . .  and a lot of stress.
An awful lot of stress !
So I seem to be in a vicious circle which is hard to get out of.
But I have to keep going – no other option. I did choose to get into property because I have CFS. (Realise that will sound odd and will explain more in another post).
I never expected it to be easy or a short-term thing. But right now it is quite a struggle.
Its difficult to get any balance in my life – like doing nice things eg. actually seeing people, friends, actually getting out of the house. Even just watching TV or reading would be nice !
I seem to be cancelling things more – or just not making any arrangements in the first place, as I know there will be a high risk I will have to cancel if not well on the day.                                                                                                                       So its not easy at the moment – but I will get there.

NB. I’m not looking for sympathy here – I just want people who know me to understand. Because I don’t think very many people do ?

Need to “Get It Out”

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I have decided to start this blog to write about my experiences of living with CFS for a long time. Partly to spare my husband and friends from having to listen to what probably sounds like a lot of moaning and whining. And also to de-stress myself and “get it all out”.  For a long time I have thought I would like to write a book. But this could take years – and I need to start writing now – to prevent me having a stress-induced nervous breakdown !

My thoughts are not really in any logical order – so my posts will just be pretty random. Of experiences and memories both recent and going back over the years.  And I would love it if people with CFS or ME would read it – as well as non-sufferers, friends, etc.  But even if nobody reads it I don’t really mind. As I have to do it for myself – to start to get all the anger and frustrations of the last 20 years or so out of my system.

But its not all going to be negative stuff – honestly – there will be funny stuff too !  And though I may mention my property work from time to time – it will not really be about that.  I plan to start a different blog about that.

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