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ME question.

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Is ME the same as CFS?

I’m confused as I was diagnosed with ‘CFS/Fibromyalgia overlap’ over a year ago but at some point in my medical notes this has changed to ME.

I tried to ask a GP before Christmas but she just kept answering me “I don’t know!” and gave no indication where or how I can find out.

Comments

  • sammyjammy
    sammyjammy Posts: 7,954 Forumite
    Part of the Furniture 1,000 Posts Name Dropper Photogenic
    CFS/ME are the same thing. What a dreadful response from your doctor!
    "You've been reading SOS when it's just your clock reading 5:05 "
  • Spoonie_Turtle
    Spoonie_Turtle Posts: 10,321 Forumite
    10,000 Posts Fifth Anniversary Name Dropper
    Is ME the same as CFS?

    I’m confused as I was diagnosed with ‘CFS/Fibromyalgia overlap’ over a year ago but at some point in my medical notes this has changed to ME.

    I tried to ask a GP before Christmas but she just kept answering me “I don’t know!” and gave no indication where or how I can find out.

    That's very strange because the NHS tends to call it CFS, or occasionally CFS/ME as a kind of concession. Whereas patient advocate groups and charities tend to call it ME.

    I personally call it ME for my own situation because of the neurological stuff* that goes on with the fatigue, but my notes and anything official still says CFS because that's what the NHS says.

    *not that I've ever seen a neurologist, but as everything physical checks out as 'normal' I have no other explanation for altered sensation and perception :huh:
  • 3secondmemory
    3secondmemory Posts: 1,484 Forumite
    1,000 Posts First Anniversary Name Dropper Photogenic
    That's very strange because the NHS tends to call it CFS, or occasionally CFS/ME as a kind of concession. Whereas patient advocate groups and charities tend to call it ME.

    I personally call it ME for my own situation because of the neurological stuff* that goes on with the fatigue, but my notes and anything official still says CFS because that's what the NHS says.

    *not that I've ever seen a neurologist, but as everything physical checks out as 'normal' I have no other explanation for altered sensation and perception :huh:
    No that you’ve said that, I’ve realised that no one in the NHS calls it ME! Thank you for that!
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