7 responses to “Psychiatrists see reasonable adaptations to CFS, label it “cause” and “maladaptation””

  1. Personal Failure

    I can’t describe how angry that makes me. I would love to see any of those researchers last 5 minutes in my body, let alone 7 years.

    My doctor sent me to be evaluated for depression. The questionaire may be fine for healthy individuals, but not for the chronically ill. They ask about sleep. Well, my sleep is broken, that’s part of my problem. They ask if you’ve given up activities you used to enjoy, but they don’t ask if you’ve replaced them with something else. I’m not hiking anywhere anymore, but I do enjoy video games and blogging. Almost every single question was skewed to make the chronically ill seem pathological.

    I walked out.

  2. NTE

    I completely agree that this study right here is exactly why I have so much trouble believing that they are ever going to figure out CFS – because if all you’re looking for is something to prove that you are right, I am completely at fault for my illness, my own behaviors are to blame 1000%, then, of course, you’re going to find something. And the fact that they can’t see that they have contradicted themselves in their own study, just makes me want to do something really “maladaptive,” like banging my head against this same damn wall for 15 years.

    Excellent post, love the new website: am wicked excited about having so many of my favorite bloggers in one place. :)

  3. Coble

    It’s a different verse to the same song, isn’t it?

    “We have largely been healthy all our lives
    It’s how we made it thru med school and still survive.
    We grew up among the smartest kids in the room.
    Even now if we don’t know the answer we just assume
    That the question you ask is somehow wrong.

    It’s not our fault if we don’t have the answer.
    Unless your disease is strep throat, tooth decay or cancer
    Unless you suffer from something we can test
    Your problem is YOUR problem.
    Maybe a lack of rest.
    Or something you ate.
    Or a parent you hate.
    Or being picked last for gym.
    Or malingering on a whim.

    It’s certainly not our lack of knowlege.
    For you see we have all been to a very good college
    or two or three or four.
    And we had an internship and seminars galore.
    And everyone we know and see are perfectly well.
    Obviously you are making up your petty hell.

    Just take a walk and drop the gluten
    Accept that you’re crazy and stop disputin’.
    Cause we’ve been to Med school and studied for hours
    And still have no answer for conditions like yours.”
    .-= Coble´s last blog ..Lipstink =-.

  4. lauredhel

    I’m guessing that was one of the SPHERE tests, Personal Failure (how odd it feels addressing you that way!) I’ve been meaning to put together a blog post on that for a while now. The shortcomings have been described in the literature, but in my experience the pharmaceutical companies who market the test directly to doctors play them down.

  5. Julie

    I’m not sure if you’ve heard about this (I checked your Twitter and HAT), but researchers are now saying that there is a virus that may be the cause (or a correlation, but either way, that it’s physical!) of CFS that they have found in 67% of people with CFS in a study compared with 3% of people without CFS.

    http://www.nytimes.com/2009/10/13/health/13fatigue.html

    There are some problems with the article, but if it’s true, maybe this bullshit won’t happen.

  6. Julie

    Oh, I’m definitely not saying they will tomorrow. I was just wondering if you’d seen it because I thought the bits about the actual genetic changes were fascinating. I get plenty of helpful articles from people about my condition, for which there will never be a real “cure,” so I don’t want to be one of those people, and I’m sorry if I was.

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