i have been mostly afraid to get myself checked out by any more urologists or doctors, because they have not been much help. (CPPS for 2 yrs). I also have very little money (i am 22 yrs old). at the same time I wonder if I may have some kind of simple little problem that could be fixed with more visits. I have been stretching, meditating, and taking hot baths lately with some improvement (i think)
is it worth it to get insurance for chronic prostatitis / chronic pelvic pain syndrome sufferers? does it cover the research that needs to be done? where should I can I go for help? I live in MN.
my history is;
CPPS for 2 years
no sign of bacterial infection
prostate is normal
urologist thought it was a muscle thing he told me to take hot baths. it didn;t work
i have had a vericocelectomy (varicocele surgery)
and hydrocelectomy (hydrocele surgery)