I was diagnosed with Hashi’s about 3 years ago.
A little bit of personal information here but hoping for some insight if anyone can help.
I was diagnosed with Hashi’s about 3 years ago. I also have dealt with what I thought were reoccurring urinary tract infections over the last 2 years, but come to find out, all cultures that have come back from labs have been normal meaning no sign of infection. A urologist was quick to try to put me on a medication that is supposed to numb/stop the “urgency” but I don’t necessarily want to just add another medication to my list. Not sure if this is an issue similar to what anyone else has or is dealing with? Thanks in advance.