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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Chronic Fatigue Syndrome Research Gains Funding, And Controversy

Discussion in 'General ME/CFS News' started by Denise, Nov 4, 2015.

  1. Denise

    Denise Senior Member

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  2. Valentijn

    Valentijn The Diabolic Logic

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    The comments are crap so far, so I added a brief "it's real" comment (objective 2-day CPET, TTT, not "fatigue").

    You have to be logged into their site to comment or vote up or down, but it's easy to do via Disqus. They'll send confirmation email, then you can make up a name, etc, and you're in.
     
    Ellie_Finesse, halcyon, ahmo and 3 others like this.
  3. adreno

    adreno Senior Member

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    Looks good!
     
  4. Simon

    Simon

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    Sound good!
     
    Valentijn, Bob, SB_1108 and 4 others like this.
  5. Riley

    Riley Senior Member

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    Can I just say how wonderful it is to have an appropriate photo! No pictures of a man in a suit yawning at his desk here!
     
    Webdog, ahmo, Bob and 2 others like this.
  6. RivkaRivka

    RivkaRivka Senior Member

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    The comments ARE bad, aren't they? Why do people hate us ME patients so much? That is so concerning.

    I did pitch my personal essay about last week's great news to the NPR "Shots" section editors, but I'm so glad they instead asked Miriam Tucker to write an article.

    By the way, the comments coming in from my essay (which got accepted by the NPR Boston affiliate, WBUR, a great radio station) are heart breaking. And none have spoken badly about the patients. The essay is here: http://commonhealth.wbur.org/2015/11/nih-chronic-fatigue-syndrome
     
  7. *GG*

    *GG* Senior Member

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    Yes, another good read!

    GG
     
  8. CFS_for_19_years

    CFS_for_19_years Hoarder of biscuits

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    ghosalb, mango, ScottTriGuy and 3 others like this.
  9. Kati

    Kati Patient in training

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    @CFS_for_19_years it just happens I can use my twitter skills but I hate having to look for stuff. So your posts are much appreciated. Thank you. It takes a village...
     
  10. voner

    voner Senior Member

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    NIH director Francis Collins was on the Charlie Rose PBS show yesterday evening and he discussed his strong desire to find out what's going on in ME/CFS, etc. it appeared to me that he had a strong personal investment in pushing for more ME/CFS research. my memory is poor and I've already forgotten some of what he had to say, but he spoke for a few minutes. he didn't get everything right about the symptoms of ME/CFS, but his intent to push hard for a significant research program on ME/CFS came through loud and clear. when he described ME/CFS patients, he cited a viral trigger and how severely some patients are affected – bedridden, etc. he did mention PEM and exercise intolerance. he mentioned how valuable it would be to discover and understand exactly what is "fatigue", because it could be applied to other illnesses that are fatiguing also.

    a side tidbit was that I thought it was interesting also that Charlie Rose asked him about his recent statements about "chronic fatigue", Dr. Collins did not bring it up on his own.

    I searched the Internet and I could not find any place where the video of him talking about ME/CFS was posted, yet.

    it certainly will be interesting to see who gets funded and what gets funded
     
    Last edited: Nov 5, 2015
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  11. Denise

    Denise Senior Member

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    :wide-eyed: I very much look forward to seeing this!
     
  12. Effi

    Effi Senior Member

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    I have seen this statement a couple of times... and it doesn't give me much hope tbh. Fatigue is a symptom in every disease. It's a normal bodily reaction. I don't think looking into a vague term like 'fatigue' would clear anything up...
     
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  13. voner

    voner Senior Member

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    @Jonathan Edwards, do you think this news about the NIH pushing to increase ME/CFS research will prompt any of the European researchers to apply for funding to the NIH?
     
    Last edited: Nov 5, 2015
  14. dancer

    dancer Senior Member

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    I agree that it's been frustrating to see ME/CFS conflated with "fatigue" - but I wonder if there might be some strategy here. To overcome the ridiculous stigma (that still seems to pervade medicine) that ME/CFS isn't real or isn't serious and doesn't deserve research funding....the mention that studying fatigue will also help those with cancer (who experience debilitating fatigue) or hepatitis, or MS, other already acknowledged illnesses may be a way to rally the support for funding for ME/CFS. I'm not sure, but that could be an angle to look at.
     
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  15. voner

    voner Senior Member

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    also, @dancer

    I had similar feelings to you about his speculation about "fatigue", I kind of cringed when he started talking about fatigue. sure seems the emphasis on "fatigue" is a artifact of the unfortunate naming of this disease in the usa, "chronic fatigue syndrome". on the more optimistic side, perhaps Dr. light's work will get further funded and help tie some of the pieces of the puzzle together. if I remember right, Dr. Collins did follow up a statement about fatigue with the mention of PEM and exercise intolerance. my take on the statements about fatigue was that he was partially trying to show how the research into ME/CFS could benefit The understanding of other diseases.

    as I said, my overall take on what he had to say was very positive. He was very strong in his statement about how much he desired to unravel the quandary of ME/CFS .
     
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  16. voner

    voner Senior Member

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    A couple other tidbits I remember from the interview. Dr. Collins said that his overall budget is $30 billion a year. He said that whereas one out of three research request for funding used to get funded, now days one out of six get funded.

    $30 billion a year.
     
  17. Ellie_Finesse

    Ellie_Finesse Senior Member

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    Very well put @Valentijn :) I have bookmarked it and will show my family, it might help them understand more. Trying to explain something so complex to them is extremely difficult. I can never quite find the right words!
     
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  18. Denise

    Denise Senior Member

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  19. ahimsa

    ahimsa Sick since 1990

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    Thanks for posting about the show!

    I saw a tweet from Dr. Collins about his interview with Charlie Rose. I don't normally watch that show but I decided I should record it, hoping that he might mention ME/CFS.

    It turns out that my PBS station airs this show at noon on the following day. Since it's not quite 11:30 AM in my time zone, the interview has not yet been shown. So it's nice to get your preview!

    Edited - Between last night and today I forgot the time. Show airs at 1:00 PM, not Noon.
     
    Last edited: Nov 5, 2015
  20. ahimsa

    ahimsa Sick since 1990

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    By the way, thanks to @Valentijn (and any others whose user names I might not recognize) for posting comments on Miriam Tucker's article on the NPR website.
     
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