r/Ureaplasma

just wanted to post here that i finally got negative results after struggling since december ❤️. all my symptoms are gone except for a random feeling of itch every once and a while. i had to advocate for myself throughout this process because no one would have ever tested me without me asking. the only issue i have now is that doctors refuse to test my bf. so if anyone has any advice that would be helpful since he doesn’t want to take antibiotics from the internet.

this is such a harrowing experience and i wanted anyone struggling to know that it is possible to get better. also boric acid helped me so much w breakdown of symptoms!

Hi guys!

Long story short I treated a Ureaplasma parvum infection in late October (so it’s been almost 6 months) I cleared it with 2 weeks doxy 3g azi and my husband the same. We’ve both tested negative urine and swab 4 months after treatment. I’ve actually tested negative 7 or 8 times between multiple swab and urine tests.

I did a biome test evvy and it showed high lacto iners and basically nothing else.

I did a protocol to flip my iners. I feel a lot better!!! Here is what remains:

Redness pain burning after sex. Esp in the urethra area

Bladder sensitivity after urinating & bowel movements *only sometimes* this pain if it happens only lasts an hour maybe two on a bad day. It doesn’t burn DURING urination but immediately after it feels like I need to go again and my bladder is sensitive.

I wake up 100% normal after my first pee of the day is when symptoms kick in and are usually most severe.

I saw a urogyn yesterday- she did a physical exam she said everything looked normal. When she inserted her fingers and pressed up at the 12 o clock position it was extremely sensitive and a sharp zap shot into my urethra. I also notice if I press on my bladder from the outside I get that “have to pee feeling” as well.

She told me she thinks I have non prevoked vulvodynia and CPPS/PFD. She wants to do oral amitriptyline 10mg nightly and see me back in 6 weeks.

Has anyone been through similar? Does this sound like it could be what she diagnosed me with? Why did I get pain when she pressed her fingers in that position?

Additionally I am in PFT- she will only dry needle me. Should I find a PFT to do internal work? Would that be more beneficial?

Any info or success stories are so welcome. Please & thank you

What's bothering you the most when you eat, drink, and or take vitamins? I can't take any vitamins, drink coffee, or have any sweetest of any kind, eat processed meats, or I'm paying in a short time

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