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...
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”.
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