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    Special Report - Online activists are silencing us, scientists say Reuters March 2019

    Dropping it in the middle of the Brexit chaos was obviously a bad move, I'm sure most newspapers are far too busy dealing with other stories. Overall it's a bit of a nothing-berder, sorry for bringing politics into it
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    Special Report - Online activists are silencing us, scientists say Reuters March 2019

    I think it reads quite well as a list of the successes of our campaigns to highlight the flaws in their research!
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    Twitter activity of Professor Blanchflower

    Perfectly sums up how I feel about it.
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    Use of antidepressants for/with ME/CFS?

    I was prescribed amitriptyline for insomnia during my first bout of M.E. - it was 10 years ago so don't remember the dose. It did help with getting to sleep but left me feeling really dopey when I woke up. My main point is that I had a dreadful withdrawal reaction even though I weaned off it...
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    Trial By Error: Some Thoughts About an Upcoming Article

    Completely agree. I'm probably repeating what others have said but this tactic allows all criticisms to be thrown aside as irrational shouting by ill-informed patients. The narcissism it must take to sustain this thought process is breath-taking; to be so confident/arrogant that you are correct...
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    United Kingdom: Science Media Centre (including Fiona Fox)

    They are working very hard for the pro-fracking side. They held a press briefing a week or so ago which produced a slew of articles pandering to the fracking companies. http://www.sciencemediacentre.org/fracking-in-the-uk-what-does-the-evidence-say/
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    Trial By Error: Some Thoughts About an Upcoming Article

    Is it Reuters by any chance?
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    Petition: Review treatment of people with ME in Scotland

    https://www.scottishparliament.tv/meeting/public-petitions-committee-january-24-2019 And this is the transcript http://www.parliament.scot/parliamentarybusiness/report.aspx?r=11911&i=107684 :)
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    UK Parliamentary debate today - Thursday 24th January 2019

    The representatives of the Scottish Government this morning were quite disappointing but the committee were very good. Not really letting them off the hook. They mentioned setting up a working group and were very concerned by the poor attitude of some doctors to people with M.E. and wanted to...
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    UK Parliamentary debate today - Thursday 24th January 2019

    If Carol Monaghan is present as invited then I don't think she'll just let them get away with the usual bluster; this could be very promising but I'll try not to get my hopes up!
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    UK Parliamentary debate today - Thursday 24th January 2019

    It wasn't updated in the parliamentary briefing pack from the Commons :thumbsdown: And they quoted funding figures for biomedical research which I think were wrong - I think they were inclusive of behavioural/psychological numbers too. ETA I realise you all picked up on this early on, sorry.
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    Thyroid, autoimmune thyroiditis, Hashimoto's

    Reference range is 0.4-4 so it's within normal limits and at the low end. Like @DokaGirl said, TSH is more of a worry if it's high because it's not being responded to. Hope this helps.
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    Does anyone else experience soreness in the back?

    No, my current relapse/second bout is completely different to my first illness, no back pain or stomach pain this time. My main symptoms now are moderate/severe POTS with associated chest pain. Both were very unpleasant but the POTS is far more disabling. Hope you find some answers/help for...
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    Does anyone else experience soreness in the back?

    I got long term aching pain in the kidney area in my first bout of M.E., dismissed as nothing by doctors. Not this time round though?
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    Advice RE claiming UK benefits, paying NI contributions

    Hi, I can't give you exact advice on your situation but can offer my own experience. In the last 12 months I have claimed contributions ESA and UC. Neither has been straight-forward, prepare yourself to enter a world that makes no sense! If UC exists in your area I think you will have to claim...
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    Patient: "The latest thinking on chronic fatigue syndrome"

    This I wholeheartedly agree with.
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    Persistent fatigue induced by interferon-alpha: A novel, inflammation-based, proxy model of Chronic Fatigue Syndrome, 2018, Pariante et al

    By coincidence I've been reading their 17-18 annual report today as well as their charity commission listing. They have appointed themselves arbiters of good science, citing success as being where what they consider a 'poor' paper/scientific endeavour appears in the media; front page vs page 8...
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    Persistent fatigue induced by interferon-alpha: A novel, inflammation-based, proxy model of Chronic Fatigue Syndrome, 2018, Pariante et al

    Yes, also it states that depression and stressful life events had no significance in the responses. ETA: I basically just repeated your quote but from a different section of the paper, sorry! My brain is struggling this morning with all this going on.
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    the devil we know DuPont/Teflon

    It was a really good documentary although such a tragic story. I'm not buying Teflon pans anymore given the harm that gets done making them. We were taught at vet school about not having pet birds in the kitchen if Teflon pans are used, the fumes kill them, like in the programme! Sadly I...
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