1. Patients launch a $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
    Check out the website, Facebook and Twitter. Join in donate and spread the word!
Never Ask Us if We're Hungry -- The Answer's Always No
There are three of us here and for many years, none of us ever got hungry. When our brains would turn to mush, when our faces would go numb, and we would start the invisible vibration which is the signature dance of ME/CFS, we knew we needed to eat.
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The Energy Disorders : Diabetes, ME/CFS and FMS

Discussion in 'Latest ME/CFS Research' started by Marco, Feb 27, 2014.

  1. Marco

    Marco Old blackguard

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    Near Cognac, France
    OK - not new research - just another of my speculative blogs - but I don't know where else to post it :

    http://www.cortjohnson.org/blog/201...ell-us-chronic-fatigue-syndrome-fibromyalgia/

    Speculation aside - if you have symptoms of small fibre peripheral (poly)neuropathy its worth getting tested as you may have another underlying and treatable condition.

    Plus Mass General Hospital are now offering objective testing for small fibre neuropathy to fibro patients :

    “These findings, confirmed by other laboratories, are the first pathological abnormalities found in fibromyalgia patients. Until now fibromyalgia has been a label based on symptoms alone, meaning no possibility of treating the underlying causes. The new findings linking fibromyalgia to SFPN may make that possible since SFPN is caused by underlying medical conditions that can sometimes be identified and treated effectively.”
    Radio and Simon like this.

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