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  1. ladycatlover

    Cochrane ME/CFS GET review temporarily withdrawn

    :rofl: :laugh: :rofl: :laugh: :rofl: :laugh: :whistle: :rolleyes: :arghh: :rofl: :eek: :rofl: :sick: :rofl: :yuck:
  2. ladycatlover

    Cochrane ME/CFS GET review temporarily withdrawn

    You and me both! ;) We have a wasp problem at home that is doing my head in, so in an over-vigilant state all the time. Hopefully they will disappear soon as we have colder weather forecast for end of the week. This is on top of journey home on Thursday in husband's uncomfortable (to me) car...
  3. ladycatlover

    Cochrane ME/CFS GET review temporarily withdrawn

    The Figures (1 and 2) I put up are for the Cochrane CBT Review. Blakemore was commenting on the GE Review being temporarily removed. I've not seen similar Figures for the GE Review. I used to be able to keep up better with this kind of stuff, but just can't do it properly any more. :cry:
  4. ladycatlover

    Cochrane ME/CFS GET review temporarily withdrawn

    If you open those charts in the Figure Viewer you get to see all the Graphs too.
  5. ladycatlover

    Cochrane ME/CFS GET review temporarily withdrawn

    Chrome. I wonder if they only allow computers in UK to access the full paper for free? Though they do offer it in Spanish as well apparently. I've tried to copy Figure 1. Figure 2 So at least some of the stuff about bias is here for people to see.
  6. ladycatlover

    Cochrane ME/CFS GET review temporarily withdrawn

    It then goes on to Authors' conclusions, Background, Objectives, Methods, Results, Discussion. It's a very long webpage. Figures 1 and 2 are about bias.
  7. ladycatlover

    Cochrane ME/CFS GET review temporarily withdrawn

    I've got the full paper (I think) from this URL: https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD001027.pub2/full Unfortunately I don't have the brain power today to read it! Actually most days I don't have the brain power to read it, very occasionally I have a half decent brain day.
  8. ladycatlover

    Cochrane ME/CFS GET review temporarily withdrawn

    I tweeted Sinéad Conneely‏... Not sure if I can get the Twittery stuff to work other than as copy and paste. :oops: Sinéad Conneely‏ @phrenohead Prof Wessely liked two of my tweets. Scoping out my profile and page? I’m hardly a big hitter. I see his wife’s incredibly awful attacks on patients...
  9. ladycatlover

    "Abnormal illness behaviour" and the missing citations.

    Just got it, it all 5 pages. Might be worth trying again? Or PM me your email and I'll try send it.
  10. ladycatlover

    Forward-ME Group Minutes – 17th July 2018

    I was surprised to see this from ME Research UK as I thought @Action for M.E. did the minutes? Doesn't really matter who does them, they should be provided a LOT quicker than they are at present. Most of what's in them is old and past it now. Why even bother if they can't be put out in a timely...
  11. ladycatlover

    Petition: Per Fink Should Not Spread Lies about ME at Columbia University!

    They missed a trick though! ;) Where's Creepy Crawley? ;)
  12. ladycatlover

    Vivid Dreams After Unusual Foods

    Occasionally I have very vivid dreams, but I've never linked them to food. Maybe I should start to think about that! Last night I had a dream that I saw a grey squirrel in the caravan field (we're staying in static caravan in a field in Wales). We saw one about a week ago, husband saw it too...
  13. ladycatlover

    Addressing the needs of patients with medically unexplained symptoms: 10 key messages, 2018

    Oh gawd, that's not going to help Liverpool ME patients! :emoji_scream_cat:
  14. ladycatlover

    A series of PACE funding FoI requests

    Or maybe they rounded it down to try and avoid anger from tax payers as well as patients.
  15. ladycatlover

    A series of PACE funding FoI requests

    Might it be worth asking DWP how much they funded to the PACE trial? Though I expect they won't have a clue, they don't seem to have a clue about anything really. (I'm sure everyone knows I've stopped myself doing a major rant here! :rofl:)
  16. ladycatlover

    Children with ME, schools and the problems of FII diagnosis

    @Tilly, saddened so much by your difficulties over your son's disease. :cry: While I don't have that experience, I can imagine at least a bit how awful it is to have a child/young person sick with ME/CFS. I will be thinking of you on Friday. The first Tribunal (back then it was for DLA) I went...
  17. ladycatlover

    BBC Wales are planning a story on ME

    I've put it on Twitter for what it's worth. ;) I begin to feel like I live in Wales these days - had Feb and most of March here, then back the end of April and going home next month... More than half the year already! Especially since we hope to get back after I've had my dental work sorted.
  18. ladycatlover

    The ME Association's continued support of the Sussex ME Society

    @Andy, I can see your comment on FB, and I'm not one of your FB friends. There are currently 43 FB comments, many of them have large amounts of comments too! FB is very hokey about what it lets you see unless you manage to force it to show all comments - even then it often doesn't comply...
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