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  1. O

    Can All These Top ALS Neuros Be Right?

    bluedog my emgs were same as yours and muscle biopsy revealed mitochondrial disease . I was having difficulty walking have you asked about mito
  2. O

    I'm back.....

    yes have a look at mitochondria dysfunction - accounts for weakness and strange bp temperature pulse issues too
  3. O

    Fifth EMG - Update

    my emg findings are similar to yours and they are saying mitochondrial dysfunction diagnosed by biopsy - might be worth considering especially if your fatigue limits your life no cure mind you so still have to get on and make the most of things wish you the best
  4. O

    Symptoms for over a year now with no diagnosis

    consider mitochondrial disease weakness and nausea diagnosed by muscle biopsy
  5. O

    Fourth EMG - Update

    Blue dog its my understanding that large mups are a sign of denervation and reinervation- you have very little spontaneous activity - why couldn't a virus have damaged yours nerves- why does it have to be als. It may be - I hope its not
  6. O

    steve had muscle biopsy . they say have mitochondrial disease - explains weakness bits of trophy...

    steve had muscle biopsy . they say have mitochondrial disease - explains weakness bits of trophy and emg - mito cocktail may help and exercise - - you might want to ask for biopsy too- not great but better to know
  7. O

    Newly Diagnosed.

    tracy im sorry and thinking about you x
  8. O

    hi just wondered how you are - need a hand? mags

    hi just wondered how you are - need a hand? mags
  9. O

    It's been 8months...

    I have this , lack of strength in my hands and arms but its mitochondrial disease there are many many things that can cause weakness. try not to worry best wishes to you mags
  10. O

    Third EMG abnormal

    yes so did I but the biopsy said mitochondrial disease and if polyphasic units are mups, they were long duration. I think in chronic muscle conditions they can be long. there was no fibre grouping in biopsy so they said no als - no spontaneous activity on emg either and a 4 year story ...
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