Post Viral Fatigue Chat & Forum

My recovery story from Post Viral Fatigue / Myalgic Encephalomyelitis / Chronic Fatigue Syndrome / ME / CFS

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  1. #1
    No2
    No2 is offline
    Senior Member
    Join Date
    Jul 2011
    Posts
    130

    OK, the past couple of months I have had some breakthroughs, feeling better.

    One of the big things I realized I needed to overcome was staying up at night; I am naturally a night person, but I was starting to live vampire hours. I have finally fought back to the land of the living.

    I am still a ways from going back to work, possibly a year or so away, but there will be a time when I will have to make the decision as to when it is safe to try. My biggest concern is losing what little LTD income I have, then relapsing. (I don't need to tell you all how terrible insurance companies can be!)

    Any advice?



  2. #2
    JR
    JR is offline
    Member
    Join Date
    May 2011
    Posts
    70

    There's not much I can offer, I'm afraid. I'm self employed working on the computer, so generally I can just not seek work when I'm feeling rough (though I feel obliged to take it when it's offered).

    I would say don't worry about this yet. It's still far off, and I think when the time is right you won't feel so anxious about it. Just feel secure for the time being in your present circumstances- worries about financial insecurity and health insurance have really not helped my condition.



  3. #3
    No2
    No2 is offline
    Senior Member
    Join Date
    Jul 2011
    Posts
    130

    That is for sure. My LTD ins co has stressed me out! Had to get an attorney to the tune of 1/3 of my benefits just to get benefits re-instated. Plus, had to do thousands of dollars of testing (out of my pocket) to establish my case; then the ins co re-instated. It is all about money.



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