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Nitric oxide and its possible implication in ME/CFS (Part 2 of 2)
Andrew Gladman explores the current and historic hypotheses relating to nitric oxide problems in ME/CFS. This second article in a 2-Part series puts nitric oxide under the microscope and explores what it is, what it does and why it is so frequently discussed in the world of ME/CFS....
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"Parents of sick children living in fear" (of exercise & child abuse allegations)

Discussion in 'General ME/CFS News' started by Dolphin, Jan 23, 2011.

  1. Dolphin

    Dolphin Senior Member

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  2. Esther12

    Esther12 Senior Member

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    I thought this had been posted recently (it's an interesting read), but I can't find it now. Maybe I saw it elsewhere?

    Well worth reading.
     
  3. Dolphin

    Dolphin Senior Member

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    Apologies if it has been posted.
    I searched for the author's name and it didn't show up.
    Nor did it show up on this domain googling the title.
     
  4. SilverbladeTE

    SilverbladeTE Senior Member

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    Somewhere near Glasgow, Scotland
    This is part of why a very hard line "No more damn bloody compromise or meekness" needs taken with the Weasels and medical profession scumbags.
    80 years ago, these same vermin would have been "euthanizing" us, and actually did.
    it's the SAME DAMN THING.
    Same bigotry, same evil, same arrogance, just a lack of the jackboot and anti-Semitism.
    They have abandoned science and compassion and therefor, society should abandon them.
     
  5. Enid

    Enid Senior Member

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    Awful to see this ignorance still goes on in certain parts. At least as an adult I could think - give me a Shaman any day!
     
  6. Esther12

    Esther12 Senior Member

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    Apologies if it's not been posted, and I've needlessly and wrongly suggested otherwise!
     
  7. Bob

    Bob

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    South of England
    It's a very sad article to read, to think that the doctors and consultants can turn such a devastating illness into a weapon with which to abuse caring parents and their already suffering children. It makes me feel disempowered as a citizen and an ME patient when ignorant and pig-headed doctors, and so-called medical experts, have so much status and power, and so little accountability.
     
  8. cigana

    cigana Senior Member

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    I completely agree. Question is, what the hell do we do?

    We need some way of inciting these parents to act - they're angry and healthy and can do something. We need to get them in touch with each other and organise central protests, preferably somewhere like the Maudsley.
     

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