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[blog] notes i brought to the doctor who diagnosed me with me/cfs
I brought my cane that day, even though I could’ve walked unassisted. I expected to be given fifteen minutes, tops. I was terrified.
Apr 13
[blog] walk, don't run: living with me/cfs
In friend circles I tend to refer to it as the "I'm Tired" disease, not because that really captures the half of it, but because it makes up 90% of my responses when my partner asks how I am.
Mar 5
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