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Chronic Fatigue is Real!

frozen dandelion

Are you surprised?

Researchers might have found evidence that chronic fatigue syndrome is a real and legitimate neurological condition.

A pilot study published in the open access journal BMC Neurology
reveals that patients with chronic fatigue syndrome (CFS) have a set of
proteins in their spinal cord fluid that were not detected in healthy
individuals. These proteins might give insight into the causes of CFS,
and could be used as markers to diagnose patients with CFS.

James Baraniuk and Begona Casado, from Georgetown University
in the US, and colleagues from other institutions in the US and Italy,
studied the content of the spinal cord fluid, or ‘cerebrospinal fluid’,
in CFS patients and healthy individuals. This fluid can be tested for
the diagnosis of various neurological diseases and infections. The
researchers identified 16 proteins that can be found in patients with
CFS but not in healthy individuals. Five of these proteins are found in
all CFS patients but none of the controls. They could be a
‘biosignature’ for the disease, which could be used to diagnose it.

This is a pilot study, but Baraniuk et al. conclude that "this is
the first predictive model of chronic fatigue syndrome to be based only
on objective data". They add: "Given the controversy over whether CFS
and its allied syndromes are legitimate medical conditions, our model
provides initial objective evidence for the legitimacy of CSF as a
distinct neurological disease."

Many of the proteins found in CFS patients are involved in protein
folding and in various neurological syndromes, which might give clues
regarding the origin of chronic fatigue syndrome.

http://www.biomedcentral.com/bmcneurol/

12 responses to “Chronic Fatigue is Real!”

  1. Good news… except for the spinal tap part!

  2. A friend just sent me your link. My blog is already in yours…Songs To A Midnight Sky. I’ve added yours in return. What a site of information and hope you have here! What a feeling of compansionship I felt reading it. Thank you!

    Pris

  3. Hi Pris! Yes, I know you from Cafe Cafe — I love finding writers I like, and then discovering later that we share something else . . . so it’s writing, and life, that we share; and illness is just a small part of these.

  4. I can’t find your name anywhere on the site. If you know me, then I must know you:-) If you don’t feel comfortable posting it, my email address can be found through my profile on the link at cafecafe. Campbell is my last name.

    I just saw the comment above, too. I had a spinal tap in 1992, two years after I got CFIDS, by a neurologist who didn’t believe in it…one of the ones who made fun on ‘my little disease’ to my face. He insisted on a spinal tap, though, because I was so dizzy–he said (while he confided to my referrer, I found out later, that he was doing it for CMA…cover my ass). It took him four times to get the needle in. I already had back problems from an injury in my early thirties and it took me several months to get over the residual pain from the test. I sure hope they devise another way of measuring this!

    Pris

  5. Hi again Pris.

    On the right sidebar of this site is a button that says “About Me” — and I am SB on the CafeCafe sidebar.

    It’s Sharon Brogan. Introvert.

  6. This is terrible, to have a disease and have others intimate you don’t have it, like you’re a hypochondriac, even make fun of it. You have some wonderful links,
    I’m going to check some of them out.

    This probally sounds like a stupid question, but I know little about this. Do you ever get better? Surely you have times when you are well. Is there any kind of cure?

    SB, I don’t want to be nosy, but which of these do you have and what is the prognosis? Can you get out and do things? I’ve read a little about this before but am not informed about it.

  7. Here I am again getting ahead of myself when scanning. I just read your last response to Pris re: ‘about me’and am going to check it out.

  8. I couldn’t find an about me link on the sidebar, I don’t think it’s there but did find a ‘personal link’. This stuff is terrible, you can’t even walk upstairs without pain??

  9. OK, so it’s a little obscure. The “About Me” button is on the right sidebar, just under the Big Sky Blog link. It’s blue.

  10. Hi All,
    I too am a member of Cafe’Cafe’ and have had CFIDS for 15 years. Pris and I met through Didi a few weeks ago, quite by accident actually. What’s been terribly troubling me this week, with the holidays approaching and my perfectionistic parents visiting for a day, is how do you guys get any housework done? I tried to do some today and am in so much pain I can hardly type. I’m going to admit to my melodrama, but I even cried today from the pure pain and exhaustion of trying to clean one bathroom. How do you take care of your houses? I used to have a cleaning lady but the price of my meds has forced me to cancel her. I can’t take it. The clutter/??mess is driving me crazy (in addition to the other symptoms of CFIDS). Any suggestions?

    thankx much,
    nancy.

  11. Nancy,

    Check the next post!

  12. I found it, and think I read it before, I remember the pictures at least.

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