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Ubiquinol?

Discussion in 'Alternative Therapies' started by Sidney, Apr 22, 2015.

  1. Sidney

    Sidney Senior Member

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    SF Bay Area, USA
    Is there any consensus about a good dosage of Ubiquinol for PEM?
     
  2. morse27

    morse27 Senior Member

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    NORTH of FRANCE
  3. morse27

    morse27 Senior Member

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    NORTH of FRANCE
    MYSTIC, Sidney and merylg like this.
  4. minkeygirl

    minkeygirl But I Look So Good.

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    Left Coast
    I've never heard of it used for PEM. My NP just told me about it for mitochondria and there's a lot of info here on it if you look around.
     
    Sidney likes this.
  5. morse27

    morse27 Senior Member

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    coq10 this has been for me the first effective drug in 2013, after the liquid oxygen remains important each night to reduce hypoxia during desaturation (74% O2) and slow neurological deterioration
     
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  6. Sidney

    Sidney Senior Member

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    Thank you - VERY interesting. I am taking only 100mg, from Bluebonnet, in the US. Fuchs looks much more serious but so far away!
    But am going to try 200...I have no pain whatsoever, but very long PEM, and fatigue the rest of the time. Thanks again!
     
  7. Sidney

    Sidney Senior Member

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    SF Bay Area, USA
    I have not been diagnosed with CFS either - I don't think my insurance in the US recognises it. My rheumatologist has diagnosed Sjögren's from blood tests, although the only symptom that I have is acute fatigue.

    I have always been active, even after polymyalgia last year - but PEM has made more than even 15 min of gentlest yoga impossible.
     

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