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

» Please tell me this can get better
New to this forum EmptySat Jul 18, 2020 7:38 pm by sammykramer

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

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

» 7 months since the diagnosis
New to this forum EmptyWed Aug 14, 2019 2:38 am by agtoronto

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

» IMPORTANT FOR UK SUFFERERS
New to this forum EmptySat Jun 15, 2019 5:21 pm by mary jane

» Help New Diagnosis
New to this forum 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 forum 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


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Post  arlee Mon Nov 28, 2011 4:05 pm

This "horror" began about 7 weeks ago - I started to have vaginal burning and discomfort. I had a Pap test and a new HVP test end of July - both were normal. My doctor first diagnosed me with vulvar vestibulitis and gave me dermovate (steroid cream) at night and premarin cream in the morning - very small amounts. After 2 weeks of this, I still wasn't better, so I went back to see her - she told me to continue with the 2 creams until the symptoms disappear (right!), and to use Fagifem 10 twice a week for moisture. I felt that the creams weren't really helping me, so I didn't use them. I had to go back to the doctor again (3rd time) - she told me that the vestibulitis is much better, but I should use the creams for 2 more weeks. She also gave me 10 mg. of Elavil to take a bedtime. I'm trying to get used to it - the first two mornings I was very groggy and nauseated. Because I've been in menapause for more than 12 years, my doctor attributes my condition to menapause and dryness. Friends of mine have been using Fagifem for years - I should have done the same. I notice in all my research (and there's been tons of it)! that the women who are suffering from vulvodynia are much younger than I. All the symptoms that I've read about point to vulvodynia for me. I am able to insert the Fagifem "sticks" with no problem. I also wanted the doctor to check my urine for excess oxalates, but she didn't think it was necessary. I would like to go to a specialist, but in my city, they're very difficult to find. I was wondering if there are any women who are postmenapausal and suffer from this awful condition. Thanks. Evil or Very Mad

arlee

Posts : 2
Join date : 2011-11-28

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