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M.E. And Muscle Weakness

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Uploaded by on Oct 11, 2010

This is yet another attempt at trying to demonstrate the problems with muscle weakness and fatigue I experience with M.E. I am not sure whether I have demonstrated it very clearly. You might need to watch in full screen mode.

I know I seem obsessed with this as I have made videos about this before. I just want to try and demonstrate what this illness is like, that it is more than being tired all the time. It also helps me to have a record. So sorry for repating myself again. :0)

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  • great video! have you ever tried the exa test? it tests the electrolytes INSIDE the cells, not in the blood

  • @kaazoom Thank you Mike. Now I know who you are on Facebook! I have so many people on my FB page I am not sure who everyone is!!

  • I have Dysautonomia and one other condition with which I have been diagnosed, is ulnar neuropathy in my left arm and hand. Just as you, I cannot hold anything in my left hand without it shaking uncontrollably. (This is just for general information). My prayers are with you and I pray someone will find a treatment that will lessen the symptoms you have or even eliminate them altogether. Don't worry about what others think, please continue to keep us informed.

    God Bless,

    Jeff

  • @FallaciesDetective Do you have a link to Dr Steve Roberts facebook page Mike? perhaps you could PM it to me. I am on Face book too. Paul Winter

  • @kaazoom

    Yes, sir! In fact they forget and/or fool us.

    But the test is not too expensive, maybe around 200EUR or pounds...

    I hope that you find a doctor who would do it and/or could send

    it to Belgium/ r.e.d. labs. There might be other labs and also there might be

    a limited time for the sending (it must be sent quick, I guess). So yeah, the best would be to go directly to the lab. God bless!

    PS: you can also try taking banjo (Dr. Steve Roberts, also on facebook , a Christian doctor, nice man)

  • @FallaciesDetective Thanks Mike. I'll have a look. The problem is trying to raise the funds to get these tests done. They should be available on the NHS, after all we paid our taxes, But as you know, the NHS doesn't care about people with ME, Fibro etc.

  • @FallaciesDetective

    PS: they can be tested in the blood, like e.g. with "r.e.d. labs" in Belgium (Prof. Dr. De Meirleir).

  • Dear folks,

    I would encourage everybody to get their

    cytokine-levels tested...(interleukines,

    like IL-1, IL-6, IL-8).

    They are pro-inflammatory and in general

    they seem to be very high in certain diseases,

    especially also in CFS/ME and Fibromyalgia ...

    all the best!

    Mike

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