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ME question.
3secondmemory
Posts: 1,484 Forumite
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.
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.
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Comments
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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 "0
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3secondmemory wrote: »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:0 -
No that you’ve said that, I’ve realised that no one in the NHS calls it ME! Thank you for that!Spoonie_Turtle wrote: »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:0
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