Takling life with Chronic Fatigue Syndrome
What happens when someone with Chronic Fatigue Syndrome and a whole host of other invisible ailments tries to keep up with normal humans for a week and a half? Let’s find out!
Living on disability comes with the added stress of knowing you may be ripped off of it at any point for any reason – completely vulnerable to the whims of someone you’ve never met.
…and many people are capable of hiding chronic pain in the same way an injured animal might if there’s a wolf looking at them.
I must admit that when the Corona Virus hit the US it was at the worst time possible for me. After a year and a half “down” where I did almost nothing except go to the grocery and feed store
Stress. Depression. Sleep deprivation. All these things and more can cause black-outs even without drinking or drug use.
So around Christmas I was feeling a little better physically and the brain fog had almost completely disappeared so I was anxious to be productive again. I accomplished nothing in 2019 which was driving me nuts. The New Year would
Brain fog, sudden memory loss, and other alarming short circuiting of the brain can be both alarming and frustrating…
Another battery of tests has revealed very little and I am wondering where to go from here..
Just when I got my own space cleaned something came along to fuck it up again…
It’s been a frustrating few weeks. My brain fog has lifted and my mind is absolutely whirring at top speed. I can’t slow down for a second, not even to breathe, as I think of more things I need to