How did Fibromyalgia become a brain disease? Disentangling conjecture and truth.

I think Clauw's wording is speculative and often clumsy but it is not circular. It is clear what he implies - what Snow Leopard points out would be putative abnormal central sensitization. And that might not be as high as brain. Genetic studies might well show a plausible basis for that.

I agree that Clauw's crowd have hyped the idea in the clinical arena but the critics are just as much wilfully blinding themselves to reasonable biological speculation.
 
Just out of curiosity since this is not my field—how would you go about controlling for those peripheral factors?
I'm not an expert on this but I'd suggest methods that modulate the excitability of the DRG and/or spinal cord independently via several methods

- Dorsal root ganglion stimulation ('placed near the cell nuclei of the afferent neurons of the dorsal root ganglia')
or tonic spinal cord stimulation ('electrical field over the dorsal columns of the spinal cord')

-local anaesthesia and steroid block of pain in the DRG (not a 100% block but partial)

-pulsed radiofrequency (heat)
 
I'm not an expert on this but I'd suggest methods that modulate the excitability of the DRG and/or spinal cord independently via several methods

- Dorsal root ganglion stimulation ('placed near the cell nuclei of the afferent neurons of the dorsal root ganglia')
or tonic spinal cord stimulation ('electrical field over the dorsal columns of the spinal cord')

-local anaesthesia and steroid block of pain in the DRG (not a 100% block but partial)

-pulsed radiofrequency (heat)
Thanks!
 
Because the issue of 'tender points' has been brought up, and this is something notable, I must say that I have never once seen any discussion of anyone having such problems in the fibro community, outside of people commenting about this being used as some sort of test, which doesn't seem to have any evidence for.

Not once. Not a single time. It's all about widespread pain, fatigue and mostly flu-like symptoms. Also some PEM. I see constant discussion of PEM, OI, POTS and other issues out of both the LC and ME/CFS. I have never once seen a single comment from someone suffering from fibro about 'tender points', or even localized pain, which I assume were mostly the product of someone's imagination, and things got out of hand, like the deconditioning and 'unhelpful beliefs' did in ME/CFS.

This feels significant to me.
 
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