Can someone please remind me why urinary retention happens in M.E. and what can be done to help?
The pressure causes me to try frequently and is in itself tiring, so adding to fatigue.
From your kidneys, ureters, bladder, and beyond- What's ME/CFS doing to your ability to pee?
If you're having urinary symptoms, feel free to answer what you're comfortable with:
* New with or after ME/CFS onset?
* How troublesome or severe?
* How often?
* Seeking treatment? Who- PCP/GP...
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