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» Acupuncture advice please
Today at 2:25 am by ryn207

» New and need some help
Today at 12:49 am by Sad

» Please tell me this can get better
Mon Feb 19, 2018 2:10 am by anon99

» Lichen Sclerosus
Fri Feb 16, 2018 2:47 am by ryn207

» MAY HAVE FOUND A CURE- PLEASE READ
Thu Feb 15, 2018 10:04 pm by infinitelywondering

» my rock bottom, psychological effects of vulvodynia, I told him he can leave me
Wed Feb 14, 2018 6:43 am by renegade_magdalena

» Some interesting information about nerve pain in general
Wed Feb 14, 2018 3:58 am by Athena

» Sore after using dilator for first time in a year
Wed Feb 14, 2018 3:45 am by Athena

» What helped me
Wed Feb 14, 2018 3:38 am by Athena

New and need some help

Wed Feb 21, 2018 4:30 pm by LindafromNJ

New to this site ad trying to figure out how it works.  I am trying to post as a new member so I am hoping this goes thru.  I am a senior adult and have just been diagnosed by the Drexil Vaginitis Center to have vulvodynia along with Vestibulitis (not sure if spelled correctly).  My symptoms are vaginal burning, itching, soreness around the vaginal opening with one spot in particular.  Some …

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MAY HAVE FOUND A CURE- PLEASE READ

Thu Feb 15, 2018 10:04 pm by infinitelywondering

Dear all,

Today has been the day I've been waiting for. The day something FINALLY makes sense.
I've been told countless times that I've got nerve damage or a muscular condition, yet none of the specific treatments have helped me. My GP suggested attacking this from a different angle so referred me to a dermatologist specialist


after having a vestibulectomy with no success, I decided to visit …

Comments: 0

NO PAIN DURING SEX

Sat Feb 10, 2018 12:18 am by rockylife

I HAVE NO PAIN DURING SEX, BUT I FEEL THIS BURNING SENSATION ALL DAY JUST BESIDE THE VAGINAL OPENING. DO I REALLY HAVE A VULVODYNIA? I'M CONFUSED.

Comments: 2

Newby not sure where to turn

Thu Feb 01, 2018 3:32 pm by Cerjo87

Hi this is all very new to me , well the talking about it bit is , the pain while having sex and also the uncomfortable feelings after and feeling like I have  sistitus most of the time I’m very used to , I’ve suffered for 7 years now I’m only 30 . Finally after all this time the doctors or should I say my gp has said I have Vulvodynia and have givin me gabapentin to try .i told her I’d …

Comments: 4

Looking for a friend..... and new problems

Sat Jan 06, 2018 11:38 pm by infinitelywondering

Hi everyone,

I hope you're doing well.

I hate to say this, but I feel beaten down and terribly alone. I had a vestibulectomy surgery about 6 months ago and I was absolutely praying it would work. It didn't.

6 months later and here I am, sitting on my bedroom floor crying my eyes out because I know I'll never be able to have painfree sex. I don't know what to do and just need a friend Sad



Comments: 8

Newbie to the site

Sun Jul 30, 2017 12:16 am by Ksa

Hello. Thank you for this wonderful site. I'm currently under the care of a dr in Phoenix that specializes in vaginal disorders. I will probably be on a suppository of estridol the rest of my life and I am currently on medications for a rare form of vaginitis that's pretty unheard of for my age. My vagina literally hates me. I've struggled with vulvadynia for 20 years, the duration of my …

Comments: 4

Vulvodynia from #metoo media coverage

Thu Jan 25, 2018 9:01 pm by dooleyhornberg

I am wondering if anyone else in this forum has experience an increase or flare up in their vulvodynia as a result of the coverage of the sexual abuse scandals in Hollywood, DC, and the recent gymnastics scandal. I have definitely had a flare up.

Comments: 0

So frustrating!!

Thu Jan 04, 2018 1:15 am by Hannah77

Well I'm back in pain after 7 years of pain free days.
I was diagnosed with vulvodynia when I was 17. I suffered for three years with horrible burning all day, painful sex with my boyfriend and just pure misery Sad I went into a spontaneous remission when I was 20. I'm still not sure how the pain stopped but all the sudden I could go an entire day without thinking of my vagina, sex started to …

Comments: 3

Looking for suggestions or encouragement

Sat Jan 13, 2018 12:10 am by ryn207

Hi there. I'm 25 and have been dealing with this for over a year and a half and I'm really starting to lose hope this will ever stop.

In July of 2016 I had a yeast infection. When Monistat didn't work I went to my gynecologist who prescribed Diflucan. When the itching didn't stop she retested me and found that my yeast infection was gone, but I now had a bacterial infection. After taking the …

Comments: 4


Vulvodynia was candida for me

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Vulvodynia was candida for me

Post  snarky on Mon Jun 20, 2011 7:32 pm

Hi everyone,

I am posting my story here in the hopes that someone else with my symptoms/background will read it and find some relief. I was plagued by vulvodynia for about 5 years and went to probably 20-25 different doctors, an utterly frustrating and at times soul-crushing experience for me.

8 yrs ago, I went on several courses of antibiotics for UTI-like symptoms, maybe 5 or so courses. I am not sure to this day if I really had UTIs, or if there was some other thing going on, but everything got much worse after the antibiotics. My symptoms were yeast-infection like: burning, itching, etc. I tried topical yeast infection creams, and they would temporarily help but then two weeks later it would be back. Eventually, my skin stopped tolerating the topical creams and I broke out into horrible burning pain. Sometimes my symptoms were chronic, sometimes just after sex, and sometimes only after sex at certain times of the month. Sometimes I would stay up all night b/c I had such bad pain (felt like poison oak or something). I was tested for every strain of yeast and bacteria and the tests were always negative, and I had no discharge whatsoever that would indicate infection. However, my doctors said I did have high levels of white blood cells, indicating my body was trying to fight something, I guess. I was diagnosed with generalized vulvodynia and also vestibulitis after many years and being lucky enough to find a doctor with experience treating vulvodynia (heads up, I found her on the website for the NVA, national vulvodynia association or something... skip the regular gynecologists and go to these people if possible. I paid out of pocket to see her and it was worth every penny).

Here's how I figured out it was candida:
- I kept a pain journal detailing the level of pain. My symptoms always got a bit worse right before and right after my period (like three days before, three days after). My doctor told me that this is the time of the month when yeast grows the most.
- Boric acid suppositories really helped me, although they didn't make things go away completely. I would use them for five days or so when things were getting bad, and my symptoms would subside a bit. Boric acid is a natural treatment for yeast infections but it doesn't have the harsh chemicals in the topical creams that are so irritating.
- My body didn't really respond to amitryptyline, making it unlikely to be nerve related. It made me fatter and more tired, that's it.
- My trigger was antibiotics, which obviously kill off yeast-fighting bacteria.

I presented this to my doctor, and she finally decided it could be candida. Originally she had rejected this possibility b/c of the negative tests for yeast (also, she thought "only AIDS patients get candida," not people with normal immune systems). But after several years maybe research advanced and she changed her mind about it being possible. She prescribed me diflucan, one tablet per week for several months. I have not really had any pain since going on this medication, so she must have been right.

Ladies, if you have these symptoms (in particular, your disease is mimicking a yeast infection), candida IS a possibility no matter what doctors tell you and EVEN IF YEAST TESTS COME OUT NEGATIVE. I don't know how it works, but it can happen. This is a demoralizing, terrible disease to have, and there's not a lot of help from the medical community in my experience, so you have to be your own advocate!







snarky

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Re: Vulvodynia was candida for me

Post  Aussie on Fri Jun 24, 2011 6:39 am

Hi Snarkey,

I too think this is yeast related, my v started after 4 yeast infections in 3 months. After a year of doctors visits I have finally convinced my gyne to give me 6 months of difflucan. I noticed a decrease in symptoms when the yeast infection flared and I went to the gp for nizoral. He took one look and said I had an infection. My overall symptoms I have been experiencing for 1 year were much less on the Nizoral, and came back when I finished the dose, thus my gyne was convinced to give me the difflucan.

I saw a lady on Wednesday who is a naturapath and womens health physio. She said I am zinc deficient which does something to the stomach acid which can make you more prone to yeast infections and less likely to fight it off. So I am taking supps for that and magnesium because I have pfd (muscle relaxant) She also said all of her v patients are zinc deficient, so there must be a link there.

Heres to hoping with the appropriate treatment of the yeast I will have success like you Smile

Aussie

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Age : 29
Location : Queensland, Australia

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Re: Vulvodynia was candida for me

Post  jules on Sat Jun 25, 2011 12:51 am

I too thought i had a UTI, went on antibiotics, developed what i thought was a on-going yeast infection for months. all of my tests were negative as well. i went on Diflucan daily for months. i used creams, gels, ointments....all made my skin burn. i tried boric acid pills (in my vagina) for quite sometime...to no avail. i had a biopsy...nothing...finally a diagnosis of Vulvodynia. i went to a specialist recommend by the National V. association..i was not impressed. i cried the whole time, while she typed everything in her computer. she never looked up to comfort me. she also asked me some very judgmental questions and then i was the one who brought up possible treatment options. she referred me to a pain clinic at my request. i have gotten the best treatment from the pain clinic. I'm sure they recommend good doctors too. So happy that you have found relief and that those treatments worked for you. here i am over a year later w/ horrific pain...on three meds for this, plus pain meds. i'm doing acupuncture and P.t. i have had 4 nerve blocks w/ no relief. the meds have helped a little on and off. its better than it was w/ no meds. i am not a candidate for surgery because i have generalized V. i would have loved to found your success. it is wonderful to hear success stories. i hope it helps others....don't give up ladies!

jules

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Re: Vulvodynia was candida for me

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