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Im had this same porblen for 3 months having a BIO on thursday since I had cancer
My pap smear was normal Thank God but dont know what causing this nightmare
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I'm glad I'm not the only one dealing with this. My problems started over a year ago with bad itching on the skin around my vagina. I thought it was just dry skin. A few months later I started experiencing itching on my labia, not just the skin, and some burning too. Then my labia became a little swollen. It's worst in the morning. If I don't shower right after waking up I feel really irritated, itchy and gross. I got checked for yeast infection, BV, and STDs. Nothing. Doctor even had me do a round of diflucan anyway in case there was a trace the test didn't pick up, and it didn't help. I changed to all cotton underwear, use only natural soaps, etc. Nothing helped there either. I'm going back to a different gyn soon to get checked again. I might change the birth control pills I take (to control PMS), but I was taking them for 2 years before these problems started. I'm an asexual virgin so it feels ridiculous that I'm dealing with so many issues!
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Hey did you ever find out what the problem was? I have the same exact problem. No yeast or anything. Complicates sex. I've tried tons of water which sometimes seems to help. Other than that it's a mystery.
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I am in the beginning stages of "something", and from what I'm reading online since my Dr.'s visit with the symptoms I'm having (burning vag & labia), I'm thinking I have either Vulvadynia or Pudendal neuralgia. I started feeling something brewing down there about six weeks ago. Not pain, but a little tinge, almost like a quick weak electro shock (I know, weird) under my right labia when I moved on my chair at work. Not all the time, but enough that I was conscious of it, and mentioned this to a close co-worker. This went on for two weeks along with slight burning and uncomfortable sitting. I went to my primary who just prescribed an antibiotic without even looking down there. I guess my urine had an "elevated" WBC count. I got a call from the office that said the urine was negative, stop the antibiotic and go see your gyn. I called the office back that night cause it got worse and thought if my WBC's were high, how could it not be positive? I spoke with the Dr. on call and he said it WAS positive and to keep taking the antibiotics. I decided to go to my Gyn two days later. She looked at the area, and said there was a white skin looking patch there, and that I had an autoimmune issue. Stop the antibiotics. She diagnosed me with Vulvitus and prescribed me a steroid cream, and said to take oatmeal baths. The following day was the worst ever. I couldn't stay still, I kept walking up and down the hall, around my dining room table because I was in so much pain and discomfort, I wanted to kill myself. Once again I called the on call Dr, and asked her if I could possibly have Vulvadynia. She said I have all symptoms of Vulvadynia except for one thing. My pain came on Acutely vs Chronically. She told me to get Lotrimin at the pharmacy, and put on with the steroid cream. When I woke up the next day, it was a 90 degree reduction in pain, until I started to walk and sit. Since that day it's not nearly as bad, but I realized the more I touched the area with the creams, the more inflamed it got. I suggested other possible conditions I could have to Dr., because with these symptoms, there are a lot of things this could be. She saw me once again 4 days later. She said the white patch was gone, and that in all her years in practice, she's never seen anyone with symptoms like this and with no discharge. She said it was "strange". She now diagnosed me with Vulvadynia. She left me a VM last week saying "were grasping at straws here", but please make an appt to come in for a pelvic transvaginal ultrasound. I am going today after work. Not feeling hopeful, and ready to call a specialist who is in NYC.

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I had the same thing, it's bladder spasms. With urine left in your bladder it burns... I'm on a script for bladder spasms. It works
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Ladies, I have had vaginal burning all my sexual life. I'm 50, and I finally have the answer! It's a pelvic floor issue--my muscles contract when I have sex, or a UTI, etc. and they won't release. The stress and frustration of the burning makes it worse. A physical therapist finally solved my issue. She showed my husband how to stretch my pelvic floor muscles with his fingers in my vagina. We do this a few times a week in the evening while watching TV. It has been 2 years now, and sex is better than ever.
In my early 20s my pain was diagnosed as an allergy to my husband's semen because I always burned after sex. In my 30s and 40s I was in and out of the doctor's office begging for a treatment, but there was no infection to treat. I would self-treat, not knowing that treating for yeast causes a bladder infection, and vice versa. Sound familiar? FINALLY, pelvic pain has been noted and researched. Look for a pelvic pain & Incontinence clinic. Be aware, you don't need Kegel exercises, you need the opposite--stretching.
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Gosh. What a strange feeling with all checks done and nothing found. So confused. Started the pill again, that's all I can put it down too????
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Did you ever find out a cure?? I have EXACT same thing ok to touch but feels like nerves
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I'm glad you've found a solution! That's wonderful. How long did the therapy take? My Wife has had the issue for at least a year, not more than two. It's a little more than burning, it's completely unenjoyable for her. Clitoral stimulation is fine, but penetration beyond a completely still pinky-finger causes immediate pain and a knee-jerk reaction from to remove the stimulant. Sometimes even touching on the outside/vulva/labia (not majora) area is sensitive, and painful. Numerous doc visits and tests have finally came to the same conclusion, the pelvic floor issue. She's started therapy, and it looks hopeful, but due to a tight schedule she cannot go very often. She's maybe been 4 times total in the last 2 months, and had another visit today. We try to do it on our own when we can, but she's new to it and I don't know many techniques or remedies or anything like that. The only thing we know are adductor leg muscle massages, labial and pelvic-muscle massages, and a multi-size wand/vibrator to help stretch, but it cannot be wiggled around without pain. Do you have any suggestions, or resources? We are desperate, and hopeful that we can be back to having sex within 1-3 months.

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look at the pelvic-floor issue posts from between 9/15/16 and 10/7/16. We are having a similar problem, docs said the nerves hurt because the pelvic-floor muscles are so tight that the areas around them swell, and the nerves become hyper-sensitive. Therapy seems to be a common thing I read in threads about this, and they always seem to come from people who found a solution.
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Have you researched Lichen Sclerosis?
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Yes, I am a vegetarian too. Am considering bringing in fish & yogurt into my diet because of this. :/
This has ruined my chances of ever being intimate again. This sux. No UTI, No Yeast, No STD, 44 and my life has ended.
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i need help these are my symptoms plus my clitoris is red and bleeding sometime no infections meds burn i put in so stopping them please help
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Did y find out what was causing the pain?
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I had a vulva biopsy and was told i had sebboriac dermatitis Did yogurt any relief? If so with what? Im going nuts over this Ive lost 45 pounds from changing my diet but the burn is still there thanks for any response
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