Reality of Life With ME/CFS

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[@clubadv]

SO sorry I don't have your name, you didn't introduce yourself. I remember feeling the inflammation (encephalitis) in my head. TO ME THAT WAS THE WORST PART. I couldn't think or even enjoy TV anymore. It is no more for me. ****By the way, my protocol story is freely available online and corroborates Stanford's ME\CFS research as shown at the recent symposium. The inflammation ended when I reset my immune system. I recovered from a bed ridden state for several years and I teach what I did at @t and even give video chat for free to fellow sufferers. You can also Skype me at username KnowAPR if you like. Hope it helps someone.