Vulvodynia Support
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» Hope to all my suffering ladies
So glad to know I am not crazy! EmptyFri Oct 23, 2020 12:04 am by ringostarr26

» Please tell me this can get better
So glad to know I am not crazy! EmptySat Jul 18, 2020 7:38 pm by sammykramer

» By no means cured, but doing much better!
So glad to know I am not crazy! EmptyMon Mar 16, 2020 1:26 pm by tinkerbelle2

» How I cured my Vulvodynia!
So glad to know I am not crazy! EmptySat Dec 07, 2019 11:54 am by Millie

» 7 months since the diagnosis
So glad to know I am not crazy! EmptyWed Aug 14, 2019 2:38 am by agtoronto

» Gabapentin Gel. or other topical creams
So glad to know I am not crazy! EmptySat Jun 15, 2019 5:22 pm by mary jane

» IMPORTANT FOR UK SUFFERERS
So glad to know I am not crazy! EmptySat Jun 15, 2019 5:21 pm by mary jane

» Help New Diagnosis
So glad to know I am not crazy! 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!
So glad to know I am not crazy! 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


So glad to know I am not crazy!

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Post  Linder Sun Mar 04, 2012 7:38 pm

I have been suffering for approx. 7 years now. Pain started after I got a hysterectomy. Like 3 months later I was in emergency room as It felt like my clitoris was going to explode. Then the pain would sometimes move down a little bit. Dr. in emergency room told me that they could give me a shot to kill the nerve however it would make all numb down there. I didn't think that was the right thing to to. He also informed me I was basically doing this to myself. That stress aggrevated it and I just needed to chill. So over the years I have suffered with it and used lydocain gel thinking I was doing this to myself so deal with it. However I have really been hurting for like a week now. Out of lydocaine. I got on a medical site and asked for some relief. Was then told it sounded like I had volvodynia. OMG! I went to the medical websites reading on it. There is a name for what I have. How I feel. Its not me beating myself up thinking I am doing this to myself. I am so happy I found this site and would appreciate any and all advice anybody can give me!

Linder

Posts : 1
Join date : 2012-03-04
Age : 65

http://ransom@centurylink.net

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Post  Kam10 Mon Mar 05, 2012 12:31 am

I'm so sorry to hear how long you've been suffering without getting help. It is definitely not in your head. It's so sad doctors tell this to us and don't know anything about this conidtion.

You also might want to research clitorodynia, if you haven't already. I think it's still considered vulvodynia, but it's a subtype of it. How vulvodynia is classified always confuses me. It seems like everyone has their own way of classifiying and labeling this condition along with the subsets of symptoms and pain.

I wish you luck in finding a doctor that can help you.
Kam10
Kam10

Posts : 32
Join date : 2012-01-16

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Post  naomi Mon Mar 05, 2012 10:45 am

welcome to the forum Linder!

I hope you find support here. theres a facebook group (secret one) we set up so you're welcome to join us there too. just message Sebby or me xxxx
naomi
naomi
Moderator

Posts : 262
Join date : 2010-04-09
Location : Cheltenham

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