I am new here and I'm not sure if I am in the right place - I haven't been diagnosed with ME/CFS or Fibro or, well, anything specific yet. All I have is an ever increasing list of bizarre symptoms, and medical bills, and frustration. The most recent developments have been POTS and...
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...