Vulvodynia Support
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» Hope to all my suffering ladies
New to this, here is my story. EmptyFri Oct 23, 2020 12:04 am by ringostarr26

» Please tell me this can get better
New to this, here is my story. EmptySat Jul 18, 2020 7:38 pm by sammykramer

» By no means cured, but doing much better!
New to this, here is my story. EmptyMon Mar 16, 2020 1:26 pm by tinkerbelle2

» How I cured my Vulvodynia!
New to this, here is my story. EmptySat Dec 07, 2019 11:54 am by Millie

» 7 months since the diagnosis
New to this, here is my story. EmptyWed Aug 14, 2019 2:38 am by agtoronto

» Gabapentin Gel. or other topical creams
New to this, here is my story. EmptySat Jun 15, 2019 5:22 pm by mary jane

» IMPORTANT FOR UK SUFFERERS
New to this, here is my story. EmptySat Jun 15, 2019 5:21 pm by mary jane

» Help New Diagnosis
New to this, here is my story. EmptySat Jun 15, 2019 5:07 pm by mary jane

» 6 days post Vestibulectomy - Is this normal?? please tell me about your postop healing process!
New to this, here is my story. EmptyTue Jun 11, 2019 12:56 am by VVSSufferer

Gabapentin Gel. or other topical creams

Thu May 10, 2018 9:43 am by Rosie21

Hi I have been suffering for some years with this abominable pain. I have tried most of the systemic drugs , I asked specialists and Doctors if I could at least try a topical treatment but because this requires a special prescription have been refused Has anybody had a chance of trying these? Thank you I will try to put a link on to some of the research into Gabapentin Gel. Thanks.

Comments: 2

Putnams 'bony parts' cushion or Putnams 'Dr Huff' cushion - which is best?

Sat Aug 01, 2015 4:17 pm by Fielder

Hi everyone,

I'm a newbie.  I live in the UK.  

I'm trying to work out the best cushion to get for my vulvodynia.  I suspect that I could have pudendal nerve involvement (the aching and burning pain is from vagina to clitoris) and I have rectocele and some tailbone pain too.

I have seen some good reports on older threads regarding the Putnams pressure relief cushions....with some ladies …

Comments: 11

An absolute success story- please read!

Fri Mar 08, 2019 10:57 pm by Persevere1990

Dear All,

I posted on here back in March 2017 having just got a diagnosis of vulvodynia after a few months of relentless and acute pain. I was desperate, I was hurting, I was scared I would never know life without pain there again.

I tried creams, acupuncture, numbing gels, frozen pads, baths with various internet recommended concoctions- convinced myself I had lichen sclerosus, herpes, thrush- …

Comments: 0

I'm sorry im rambling

Thu Feb 21, 2019 5:49 am by Jet227

hey, im 19, ive been struggling with this almost a year. The first week I became itchy I went in to check about a yeast infection another week later. I have been to 10 different doctors a total of about 15 appointments for this problem for the past 11 months. I have been tested for everything including having a biopsy. I was first told basically to just go home and use hydrocortazone, then I went …

Comments: 1

New member need advice please

Thu Feb 28, 2019 11:33 pm by PANDORA123

Hello, I have just been diagnosed with unprovoked vulvodynia. Im really scared and worried. It burns a lot and it hurts to sit down. I have been prescribed amitriptyle 10mg. Can anyone give me some hope that I can get better from this condition. Feeling low and depressed.

Thanks

Comments: 5

MonaLisa Touch

Fri Feb 08, 2019 7:35 pm by rl2091

Hi All,

I'm wondering if anyone has any experience with the MonaLisa Touch treatment for Vulvodynia? My pain started when I went on HRT(pill) for anxiety mainly and my pain abruntly stopped when I stopped HRT. However, when I started on the HRT patch (at my dr's suggestion), the pain returned and has never left. That was 7 years ago. I found MonaLisa Touch on the internet purely by accident …

Comments: 3

Diagnosed Recently

Tue Jan 08, 2019 3:55 pm by flissyg

Hi All,

I’m so glad I’ve found a place where there are others who understand how I feel!

So this is my story:-

I’m 36,  and 4 months ago, whilst innocently sitting in bed reading I experienced a very sharp stabbing pain in my clitoris. It last only a few minutes and then subsided as quickly as it came on. It put it down to “one of those things”.  The following morning I woke up …

Comments: 4

New and need advice and help

Wed Dec 05, 2018 3:26 pm by Cin124

Hi everyone,

About three months ago, I started having vaginal and vulval itching. Then, about two months ago, my vulva started to feel painful and look swollen, so I went to the doctor. I was tested for herpes, chlamydia, and gonorrhea which all came back negative. I also had to do a vaginal swab test and the only thing that came back positive was yeast infection. I was prescribed hydrozole …

Comments: 6

New here would very much appreciate advice at the end of my rope

Wed Jan 09, 2019 9:09 pm by Jma990o

This might be a little long but it's been such a long time I've even been able to talk about my problems openly thank you in advance for any helpful advice.
So ok I'm 24 I've been having this problem for over two years seen quite a few doctors and obgyns alike and nobody will take me seriously I have had a few utis and yeast infections and even bv once and this all started after one of the utis …

Comments: 3


New to this, here is my story.

2 posters

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New to this, here is my story. Empty New to this, here is my story.

Post  NJay12 Thu Nov 01, 2012 6:09 pm

I used to be a healthy person who rarely got sick. My worst (and possibly only) health diagnosis I have really ever had is hypothyroidism which was discovered a good 5 years ago. I take levothyroxine daily ever since the discovery and have been fine since. However, a year ago I started feeling a pressure/heaviness in my pelvic region. I went to the doctor who ran a bunch of tests and couldnt find anything other than an ovarian cyst in which they told me was the cause of the pressure/heaviness in my pelvic region. I accepted that answer, however, a month or two later my vulva became enflamed and sore. It's never really itchy, just very red and sore. I went back into the doctor who diagnosed me with a yeast infection. They gave me diflucan and an over the counter prescription cream to use-- which didnt help. I went back in after that dosage was done and they told me that they didn't see any yeast but they would give me another round of prescriptions anyway to see if it would help clear up any small amount of yeast that might be left that they're not seeing. This again, didn't work. I am married and have been with the same partner for 7 years but I had them run STD tests anyway, just to rule that out and those all came back negative. No UTI, no BV, everything was clear. Eventually the soreness and redness either went away or at least toned down because I didn't notice it anymore. Until a few months later it came back- again another round of yeast meds for yeast they found- again it not helping, but then eventually weeks down the road going away. It came back for the 3rd time a month or so ago but this time it came back with urinary symptoms which I was then diagnosed with a UTI. (They didn't find any yeast this time so no yeast meds this round.) I've never had a UTI before in my life, but after having this one I realized thats what the original pelvic pressure/heaviness was that I was feeling at the start of this. It was the exact same feeling- even though when they checked me back at that time, the cultures and tests were all negative. Anyways, after trying 3 different medications it finally cleared up the UTI and the urinary symptoms went away, but the vulval soreness and redness is still there. My gynecologist explained to me the condition of vulvodynia, showed me the ropes on using the right soaps, buying the right underwear, etc. (which none of that seems to help.) and now, even with no UTI, the urinary symptoms come and go. I think it MIGHT be related to my hormones and my cycle- as I notice the week before my period and the week after the vulval irritation is horrible. But at any rate- I am accepting the answer the doctors are giving me which is vulvodynia and IC.. it just still shocks me how it came about out of nowhere. One day i'm fine, and now im battling this. One thing I had noticed since the start of all of this was it was also accompanied by lower back pain. I recently decided to see a chiropractor to see if that would solve the issue but all it's really done is taken away the low back pain. But I'm also on my 3rd week at the chiro so maybe I just need to give it time...

I'm so glad to have found this forum. It's nice to hear from people with similar stories as mine, even if it is unfortunate that we have all come together over this very annoying issue..

NJay12

Posts : 1
Join date : 2012-10-26

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New to this, here is my story. Empty Hi! And here's my story

Post  angrybird84 Thu Dec 20, 2012 9:11 pm

I'm new here too. Your story sounds similar to mine, so I will share ... and I think you'll understand exactly where I'm coming from.

About a year and a half ago (August 2011), I had a short-term relationship which I ended because the guy was an asshole. It was after I slept with him I started noticing severe vaginal irritation. I went to the doctor who prescribed creams. Nothing helped. It turns out it was a yeast infection, but one dose of diflucan and it was gone. And then shortly after, I ended things with the guy.

Less than a month later, I met my current boyfriend. We'd been having sex for about a month and everything was fine with that - no burning with this man at all (before I go on, I am "unofficially" engaged to this guy now!). However, I went in for a routine urine test in January of this year ... just to check to make sure I got no STD's from the previous guy. I never heard anything about the results from my doctor, so I figured everything was fine.

On the evening of February 10th at exactly 6 p.m., my whole life basically went out of control. That's when I first noticed the terrible burning after I went to the bathroom. (Don't mind me with my exact knowledge of dates, I'm OCD and I'm a news reporter). Over the next 24 hours, it progressed extremely quickly. While at work the next day, I started noticing huge amounts of blood in my urine and I almost fainted from the combination of the pain and just looking at the blood. One of my coworkers used our radio station's community cruiser to drive me to the nearest hospital ... it was kind of funny, but heck, we promoted our brand at the same time. My boyfriend rushed down to the ER to meet me, and after about two hours, I was given a diagnosis of a UTI and handed Macrobid, and then told to "eat a bagel" and go home. Going home was hell. I couldn't sit and when I got home, the pain tripled in intensity. This is coming from someone who has a congenital heart condition and has had three heart operations - I'd never felt anything like this in my life.

In the end, it eventually calmed down that night. The antibiotics seemed to kick in immediately and so did extra-strength Tylenol. I stopped peeing blood by the next morning. But then the symptoms never went away entirely. I kept returning to the doctor or the nearest emergency department, only to be told the UTI wasn't gone and they would put me on additional rounds of antibiotics. Then a few days later, I'd get a call saying I didn't have a UTI and to go off them. This happened THREE times, and over a period of four weeks, I must have seen my family doctor and the ER department at least eight times. One time I was admitted for the day and given an IV morphine drip - but all that did was make me itchy, exhausted and nauseated! I remained in severe pain, between the burning and stabbing sensations. There was also a guess from my family doctor that I may have passed a kidney stone, but a CT scan showed my kidneys were clear. A bladder ultrasound a month later showed there was nothing wrong there either.

In the midst of this, I found out from a resident at my family doctor's, that my urine test had come back positive for infection, and NO ONE called me. I am disgusted to this day, because now I believe my vulvodynia could have been prevented if this infection had been taken care of immediately in the first place. I am continuing to look for a new family doctor, because my current one has been useless and has not taken any initiative in helping me get back to normal. The other problem was I was having trouble going into work. Working at a radio station means you've got interns nipping at your heels all the time. I didn't want to call in sick because I knew that meant I was putting my career in jeopardy, but there were literally days I could not get out of bed.

This story is getting extremely long, so I will get to the point. After what must have been 10 specialists, four rounds of STD tests, 10 urine tests, and god knows how much else, I saw a specialist yesterday who diagnosed me with vulvodynia. It has been one hell of a year ... the pain never goes away for more than an hour, but even then, the area remains sensitive. There are some weeks where I work very hard to function normally, and other weeks where I can cope well. I was better for a few weeks in April, and then from September to the middle of November, but my boyfriend and I had sex three times in a week and then suddenly, I was thrown back to the way I was in March. I tried not to let it get to me this time. I've just been promoted to news anchor at my job and I can't let this get in the way, so I don't. I work through it, even on my worst days. I just make sure I have an ice pack with me at all times, and that I don't wear jeans.

Dealing with two chronic health conditions is a pain in the ass, but at least I know this isn't all in my head. I'll be tested for IC in a few months. Dreading the cystoscopy but what else can I do? Besides, at this point, whether I have IC or not won't make much of a difference. It will just give me peace of mind, knowing I won't be tested for a million STD's anymore.

This is how vulvodynia has affected my life:
-I haven't worn jeans or belts in 10 months. Doing so causes such severe pain that I only last for a few hours and then suffer for the next day or so.
-My boyfriend and I rarely have sex. He worries every time we do that it's his fault I'm in pain, because these issues only came up since we've been together. I feel so bad for him. Luckily though, he is EXTREMELY understanding and never complains. Don't know how I found such a good man!
-I carry an icepack with me at all times, even in the newsroom!
-I can't wear tampons during my period.
-My periods are absolute HELL. The combination of the blood on the pad burning my skin and the feeling of the blood coming through my vagina is horrid.
-I can't go swimming or dancing - swimming is not a big deal, but I love to dance, so that sucks.
-I can't sit through movies. I love baseball and football, but I usually sit through games in severe pain.
-I have to drink a lot or it burns like hell (both inside and outside) when I pee. Tea makes it sting, but I won't give it up because it's the only thing I can drink in the morning.

However, I think I'm coping quite well with it otherwise. In the past year, I got a major promotion at work and achieved my career goal - at the age of 28!, had my boyfriend set our wedding date (the ring will come soon!) and enjoyed an incredible road trip - even in severe pain!

Every day, I try to focus on what is so good about my life ... focusing on that helps to alleviate the pain a little bit. Not sure how I'm going to go about my treatment because everything costs so much money.

angrybird84

Posts : 4
Join date : 2012-12-20
Age : 39
Location : Canada

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