Thank you all for you replies. I don’t mind hearing different opinions. Even if your suggestion can help only in a few symptoms it is still valuable for me.
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Hi Janie, have you noticed any evolution in your symptoms these past few years? I also have PSSD and will hopefully be getting a qEEG soon so I can determine which brain structures to target with light therapy. Hope you’re seeing improvement. sending resilience your way.
Yep diagnosed with CFS too and had severe MCS.
Thanks. After B6 toxicity only Andy Cutler chelation helped in sleep, in the past years I needed to keep recovering from both reactions. I was much better before the B complex IVs with PSSD then with PSSD+severe toxicity after B complex. In past years unfortunately PSSD did not change really. Maybe cognitively clearer, no brainfog anymore but diagnosed with CFS after the B6 toxicity.