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My guess is, when you do too much, your brain releases adrenaline to keep up, and adrenaline is known to create a “warm” feeling as it makes blood go to the skin. Similarly to how some people blush (face gets warm) when they are embarrassed because they then release adrenaline, same mechanism...

They must! because as someone in Switzerland I get this as the main description: “ A disease characterised by profound fatigue, sleep abnormalities, pain and other symptoms that are made worse by exertion. Chronic fatigue syndrome occurs more commonly in women. The cause of this condition is...

I appreciate the answer, thanks you. I would say though that Mayo Clinic (which I believe is the only source cited) has changed their stance on ME quite drastically recently, and that the past few years have seen a very positive shift in public and medical perception of ME, so maybe there is...

When you search me/cfs, cfs, me etc. on google there is a popup info that reads “Chronic Fatigue Syndrome”. The only medication listed under the “Treatment” section is “Antidepressants”. The “Speciality” section reads “Primary care, Psychology, Clinical Psychiatry”. There is a feedback section...

I honestly don’t understand why researchers are so obsessed with SSRI’s in LC (and ME/CFS), as with GET/CBT if they made a large positive impact we would definitely know by now.

My PCP put me on SSRI’s to help my LC even though my mood was fine and I was feeling as mentally good as you can given the circumstances. My symptoms worsened, she kept on dismissing it until testing showed I developed serotinin syndrome. Only time will tell but i think that permanently worsened...

Yes lets bombard with ME and LC :)

this is amazing! how do we know what happens next though? What are the next steps? I’ve been disappointed too many times with ME and im terrified of a “poop out”.