Weird Tingling sensation in my Vagina

See if you can get a prescription for Oxybutynin. It helped me and my symptoms were almost exactly like yours. Oxybutynin reduces spasms and is often used for incontinences. But it works for this as well. The only thing is that it makes me thirsty. So I'm always carrying a bottle of water with me. The good thing is that after taking it regularly for 2 months, I found I didn't need to take it as much. I use it as needed now.

I'm not a Doctor.

If you're having a UTI/ yeast infection you'll probably know. Some times, some people will have other symptoms that don't fit. Or other symptoms that don't show. From my most recent experience I can attest to this. I'm prone to both UTI's and yeast infections so I know very well what they feel like and how they present. This was different. This caused extreme pain urinating and some other not so enjoyable symptoms.

I had a lot of pressure in the under carriage (pelvic floor) like the feeling of sitting too long and a charlie horse combined.Tightness in my anus. Like I had turd up there that wouldn't come out. But, when I went, only a little came out. The area under my butt checks felt like when you sit too long and when you get up the blood rushes back to it and it's almost not quite painful. The feeling spread down the backs of my legs. My toes started to hurt. The beds of my toe nails ached.

Arousal. I wasn't sure if it was the pressure from the constipation pushing on my g-spot or what but I had that deep intense arousal feeling. Masterbation had little effect. At one point I layed down and my clit started to build with endorphins like a flash orgasm over and over again so I couldn't sleep without jolting from the sensation.

At this point it's a big wtf.

So here's what I've got.

I'd started on Nitrofurantoin mono which had a possibility to cause the neuropathy in my legs and feet but the sensation started in my lower butt before I received the meds. Take what you want from that. But no mention of any arousal side effects.

From what I've found through research, there are many and no reasons for your broken bits. PGAD and pelvic floor problems seemed like a symptom of something that wasn't there before. (Some people might just have PGAD or pelvic floor problems). However, tightness, neuropathy, pain, arousal. Those symptoms align with your Pudendal Nerve. Something happened where this nerve was irritated/pinched and cause everything to go haywire. Chronic UTI's/ yeast infections, in my case, I believe caused this. There is a lot of causes/reasons for s**t to go wrong down there so see a doctor. But, for the purpose of explaining what people are feeling I believe the Pudendal Nerve is the answer. Again, see a doctor.

Sorry to hear you are going through this. My thought what it may possibly be, (because I go through it) is interstial cystitis. a chronic inflammation of the bladder wall. when I have a 'flare up' it is very frustrating since it causes my bladder to flare and also makes me have unwanted arousal. I was diagnosed in 2006 by a urologist after going to many doctors. good luck in your journey. I hope it's not something like interstial cystitis or worse.

I'm so sorry to hear that, ive been going through the same thing.

Does anyone know how to get rid of this?

I have the same problem. I cant sit straight anymore its extremely uncomfortable. please help I have already done a round of antibiotics but the problem didnt go away.

i really need to tell you all my story. ive lived with this and its taken over my life he past to The point I’ve felt like ending it all. When I was 17 at college, happy stress free happy relationship etc, I started getting the constant tingly sensation in my clit area, I didn’t think much of it but it persisted for days so I looked it up and found PGAD if I’m honest I’ve always regretted looking it up because it made me so scared and my life was pretty much a depressing whirlwind until I was then around 20. It would show up on and off and would stay for long periods, days , weeks, months. I did suffer with lots of water infections and was told I had IC. I really didn’t feel like this matched with my PGAD though, I never knew how to tell the doctor so always found myself saying I had strange sensations but never honestly saying in my clit. It’s scary, I’m shy etc.. when I was around 20 it subsided for a while- at this point I thought maybe it was phycological because I became very distracted at 20 with my bf and lots of drama in my life, however it snuck back on me. When I was 23-24 it came back bad I was hysterical and so I told the drs I was depressed and went onto anti depressants and it subsided. I went travelling and lived in Australia and diff countries and now an then would think bout PGAD but quickly stop and it only reared its head now an then and I could get rid of it... but now I’m over 30 and it’s back with vengeance. This is probably the longest I’ve gone without it but it’s now back and has been for over a month now. Constant arousal - makes me uncomfortable around my friends, makes me anxious panic attacks.. and now I have split up with my boyfriend and am moving out because it makes me that scared and depressed I can’t be myself, I can’t tell him or anyone. Finding this forum does help knowing I’m not alone but I worry I become obsessed. I purposely got so drunk for past week as it’s only way I can forget it. For years this has hung over my head. I’m going to contact my drs and tell them I’m depressed again and see if anti depressants help again. Honestly please know I am with you on this. But I am wondering if once you read up on PGAD we get obsessed? And makes it 100 times worse. I can’t bare it though and I didn’t even think about it for it to come back this time. I had hoped it was just hormonal changes as I grew up but now a full month with it. It makes me want to end it because I can’t focus on work, my love life, my social life. I’m so sorry to you all it did pass for me for years. So it can for you. I just don’t know why it’s back

Hello. I have been having the same sensations you have had since March 2021. I hadn't had sex for over 3 years, but reconnected lately with a previous lover. I thought I had a UTI, even though in over 40 years I had never had one. I went to my doctor. I had a UTI test which is peeing in a cup. She prescribed Cipro before the test results because we really believed it was a UTI. It took a few days for the test results. In the meantime I took the Cipro as directed. It helped! I felt relief. When she called me she informed me that the test results were not a UTI. It was a bacteria. She would need to do additional tests. However, I said the meds were working and I was fine. Two months later, the same symptoms were back. I did a yeast infection treatment to no avail. I went back to the Doctor. I asked her to do an STD test. I told her not to prescribe anything until the test results. For a week it felt awkward at the end of peeing. Today she told me that the test results are Mycoplasma Genitalium. It is an STD or STI that is relatively new. I have now been prescribed Azithromycin or Zithromax. I told my bf and he said he thought he was having prostate problems. We are so happy we have hopefully found the answer. I hope this helps.

Hi im goin threw this right now whats is this my vagina feel weird something i never felt before tingling sensation down there please help explain?

it is infection. I have being battling with vagina infection for years. Tired different treatments all to no avail. But today with a Chinese product I am free. If you will like to know the product and purchase it. Drop your comments.

hi. I've had these symptoms for the last 15 years on and off. mine, I think are stress related. I seem to get them when I have a lot of stress in my life! I get a permanent irritation/burning sensation in my vulva and the strange almost orgasmic tingling when I finish weeing. I've been tested for UTI's in the past. I've been tested for STDs and all negative. I usually self medicate and use probiotics, sometimes drink with baking soda, eat lots of Greek yoghurt. watch my diet, and try to exercise more. It usually passes after a while but can take up to approx 2 or 3 months to go. I think I get flare ups of interstitial cystitis, although I have never been diagnosed. Docs always just put it down to stress.