Posted 7/22/2014 10:21 PM (GMT 0)
Well, pain still brutal as ever. I went to a pain doc the other day who told me I had burning mouth, glossal pharanygeal neuralgia and fibromyalgia, not lyme. But then said it's possible that fibromyalgia is really chronic lyme and was untreatable. Basically he said there was nothing he could do for me. What? Literally, I think he was just throwing darts at the dart board, and doesn't really care. He recommended I do CBT therapy online. The pain is constant in a particular location, there has to be a root cause being overlooked.
So I left him and I'm moving all my stuff to a much better place, that is taking me alot more seriously.
I literally spent all day talking to scientists, labs, the chemists. They had varying theories but one insisted that it wasn't the tea, and that was a pure coincidence.
So I'm back to square one and still miserable, can't sleep it brutal. But working on it.