The Real ME: A Stock Photography Resource for the Media
We’ve all seen them in the news stories about ME/CFS: the guy in a suit at the office, yawning; the beautiful woman sitting at her desk with her immaculate make-up and elegantly coiffed hair, hand to her head and looking slightly pained.
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Inviting you to visit my blog, recovering from CFS

Discussion in 'General ME/CFS Discussion' started by figuringthisout, Mar 1, 2015.

  1. figuringthisout

    figuringthisout

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    California
    Hi all, I just wanted to put this out there. I have been making blog posts, but never actually made my site public or indexed on google until now. I do talk about CFS a little bit, but for the most part I'm focusing on personal development and positive things. I wanted to invite you to visit it, since I have been struggling with severe CFS. I was bedridden for about 10 months and only started being able to walk a tiny bit recently. I may take down this info from here soon, so it's not up here forever, but the URL is (edit: I removed the URL now) and I'd be happy to hear from other CFS sufferers.

    Hugs.
     
    Last edited: Mar 2, 2015
  2. msf

    msf Senior Member

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    Hi, I only read your first post, and I'm glad you are getting better, but if you get worse with exercise maybe its better to put your fitness plans on the back burner?
     
    Valentijn likes this.
  3. ukxmrv

    ukxmrv Senior Member

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    London
    I'd find it a hard read as I did a lot of work on self development in the early decade of ME and I never recovered from this disease or had a remission. When I look back at that time I feel as if it was wasted and I wish that had focused on other things.

    It's a very personal journey and we all have different needs.
     
    ahmo and SueJohnPat like this.
  4. figuringthisout

    figuringthisout

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    California
    Hi MSF. Thanks for visiting my blog. I'm not working out at this time, these were just thoughts as I questioned what I might possibly be doing in the future because I've made quite a bit of progress in the past year.
     
  5. msf

    msf Senior Member

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    Hi Figuring this out, I thought that might be the case, I just didn't want to see you, or anyone else, undo some of the progress they have made by pushing themselves too hard. I can't imagine what it's like to be bedbound with this disease, but the only time I was housebound was immediately after doing strenuous exercise. Since then I have limited myself to walking, and usually for no more than 30 minutes.
     

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