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Living with Dysautonomia and EDS – Chapter 1 “Supercharged”

What living with dysautonomia and EDS feels like – “Supercharged out of my Head”

Yup you guessed it, another shitful attack. God, this body is a pain in the neck.

My meds were changed 3 weeks ago because of adrenaline issues, I had reduced my meetings and the intensity of my exercise program and was doing really well.

Then I changed something.  Moved my usual morning exercise to the evening last night, evidently when the impact of my glory wonder drugs were at their lowest, and had a sleep from hell.    Continue reading Living with Dysautonomia and EDS – Chapter 1 “Supercharged”