u/Fun_Examination5329

Drives me insane as even when my blood sugars are good I still have dry mouth which makes me drink more which makes me pee more.

Just wondered why doctors would refuse. It’s not for me just someone I know.

Or do they just send you home with painkillers.

Mine doesn’t feel hard or firm at all.

It is large though and larger than I think it should be at my weight although as I have a B Belly it’s hard to tell I guess.

Over the last few years the sensation has changed. I don’t feel pressure on my bladder when I need it’s like it bypasses that and I can feel all the urine right in my urethra. It’s not just a sensation I can ignore because there is a fair amount of pee in there ready to come out and when I go to the bathroom I immediately pee a good volume.

Any idea why I wouldn’t feel the pressure in my bladder as the first sign I need to go.

This causes me so much anxiety.

I want to increase my water but don’t want to be peeing all day.

Can you have kidney stones that are just causing frequent urination rather than pain.

Anyone find that pelvic floor therapy has improved this.

Does anyone get Mons Pubis pain that goes right down the bones at either side of the vaginal opening.

I had heard this but wasn’t sure how true it was.

So I am looking in to getting a Urostomy as but I know it’s a last resort and for me it actually is because I can’t eat without being in horrendous pain even things that are listed as safe on the IC diet.

Anyway since all this kicked off with my bladder I have tried the diet, I have tried reducing stress by working at home, OAB meds Solifenacin, Tolterodine, Mirabegron, Oxybutynin also nerve meds such as Pregablin, Gabapentin, Duloxetine, Naproxen. I also took 8 different antibiotics for over 2 years for embedded uti.

I have practiced bladder training and Pelvic floor exercises. I was abused as a child and have so much trauma that I can’t have anything in my vagina so I can’t do Botox or Bladder instillations as I couldn’t cope. I am praying my Urologist will understand this.

Has anyone had a Urostomy and not had to do Botox and bladder instillations.

Those that had the Interstim did you have to have Urodynamics before it.

I have issues in that regard due to past trauma and I am not ready for internal work but can a therapist still diagnose PFD and will the exercises still help

Can it help with Pudendal Neuralgia type symptoms I get terrible Mons Pubis/Pubic bone pain.

Does anyone get this and it feels like the worst period pain ever and not on my period or due for another 2 weeks.

I don’t get a pressure on my bladder week I need to pee i just feel the urine at the end of urethra/vagina. It’s also not just a sensation as when I go to the bathroom I do pee it out.

It’s just don’t know if this is urgency or pelvic floor🙈

I was sent for blood tests to check my blood sugar. I was sent again a week later as it showed alkaline phosphate was elevated and doctor phoned to say this was due to my low vitamin d.

Would these tests also show low Vitamin B12 as I have some symptoms I think.

I literally can’t drink anything without it coming pouring back out and full volume every time.

Anyone had blood tests and came back that kidneys were fine but it was just inaccurate.

See if you have tried everything would you be able to get bladder removal/diversion.