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This story begins, well, when I was three. I won’t force you to ride that whole road with me except as relevant in future posts. We’ll sum it up as: childhood & adolescence = very bad. Result = PTSD.
I have been diagnosed with myalgic encephalomyelitis/chronic fatigue syndrome. There is still a loud audience of people who proclaim this is not a real disorder, that patients are lazy hypochondriacs.
This is far from true and takes so much away from sufferers.
As for me, that may be my diagnosis, but I’m not sure it is. I have many symptoms that aren’t on the lists of symptoms.
This blog is my archeological site, my dig, for confirmation of my diagnosis and/or an understanding of the symptoms that don’t fit the mold.
