Vulvodynia Support
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» Hope to all my suffering ladies
Another Limey! EmptyFri Oct 23, 2020 12:04 am by ringostarr26

» Please tell me this can get better
Another Limey! EmptySat Jul 18, 2020 7:38 pm by sammykramer

» By no means cured, but doing much better!
Another Limey! EmptyMon Mar 16, 2020 1:26 pm by tinkerbelle2

» How I cured my Vulvodynia!
Another Limey! EmptySat Dec 07, 2019 11:54 am by Millie

» 7 months since the diagnosis
Another Limey! EmptyWed Aug 14, 2019 2:38 am by agtoronto

» Gabapentin Gel. or other topical creams
Another Limey! EmptySat Jun 15, 2019 5:22 pm by mary jane

» IMPORTANT FOR UK SUFFERERS
Another Limey! EmptySat Jun 15, 2019 5:21 pm by mary jane

» Help New Diagnosis
Another Limey! 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!
Another Limey! 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  *Cat* Thu Sep 02, 2010 6:26 pm

Hi Guys...so glad to have found a forum like this cos boy am I suffering!! I'm Cat, 29 next week and I'm from Swindon, England. Ok so, I haven't had an official diagnosis of this condition but in my desperation and bafflement from GP's I'm kind of at the pont of guessing the problem. For the last two months, I've been going in the docs complaining of burning, stinging, rawness and irritation...dripping feeling - and it's pretty much constant. My story is this, it came out of NOWHERE! I've gone over so many things in my head of what it could be. It's not a STI because I'm not with anyone and haven't been just before this or during. I'm not allergic to anything (used the same products for years and don't use anything perfumed down there anyway). It's driving me insane and has led me to be in tears most days. I can only think that it's hormone related and somehow, I've managed to upset the balence of the flora and fauna down there. I felt low as in depressed before this started and this has just made me feel a whole lot worse.

I've had a swab and urine samples taken (both clear! Rolling Eyes ) Initially I thought I had cystitus or thrush...but the treatments didn't work. Been on anti-biotics....nowt! Caneston cream.....rubbish and makes burning worse. Went to doc again yesterday...he had a look (Lovely...pass the bag for my head) Was sore in some points but looked at me and said 'Even though the swabs are clear I'm going to treat you for thrush again because thats what it looks like'. So got a pessary thing to try and he's shoved me on anti-depressants. I can bet you a tenner right now, I'll be back in two weeks. I was dying to say....WHATS VULVODYNIA, but why should I? He's the bloody doctor and it's a crime that this isn't more well known.

I can just about put a pair of baggyish jeans on.....but it looks like I can wave the skinnys goodbye.

What a biatch!!

*Cat*

Posts : 1
Join date : 2010-09-02
Age : 42
Location : Swindon, UK

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Post  Sebby (Admin) Thu Sep 02, 2010 9:09 pm


Hi Cat..Welcome to the forum!

Firstly I would say you need to be careful about the overuse of thrush creams as they have been linked to making vulvodynia worse as well as long term use of antibiotics. If I do get thrush I take the oral pil.

I pretty much had to diagnose myself and just had that confirmed by the gynea..u will be suprised to learn how many drs have not even heard of Vulvodynia!

At the moment I am using Co-codermol 15mg x 2 tablets when the pain is bad as I am currently wating for a nerve block injection.

Ask to be refered to a Vulva clinic, not just a gynea...you want a consultant who has treated Vulva pain before. Most GPs know little to nothing about this condition.

The girls on here give great advice! They told me to also get refered to a Pain clinic and I did..there I met the first dr who not only knew what Vulvodynia was but had also treated women with the condition!

As for clothes, myself and most of us live in leggings! I thank God they are in fashion! I wont wear jeans at all!

I have also been advised too see a women's physical therapist as there are treatments regarding bio-feedback and pelvic floor exercises that are suppossed to help.

There are a lot of avenues to go down but keep fighting and keep in touch

Godbless

Sebby (Admin)
xxx

Sebby (Admin)
Sebby (Admin)
Admin

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Age : 43
Location : London UK

https://vulvodyniasupport.forumotion.net

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Post  jules Fri Sep 03, 2010 5:29 am

Hi Cat,

Welcome and sorry reading our stories make you sad. That's how i felt when i first surfed the web to research Vulvodynia. I'm with Sebby. I would not use any more creams. I have read studies that show creams can actually make the nerves more sensitive. What you all call Thrush, we call a Yeast infection in the U.S. I was treated for over two months for a yeast infection and i didn't ever have a positive pap smear for yeast. My doctors just didn't know what else to treat me for. When i used at least 9 different creams over a period of time, my symptoms got way worse. I would agree to only use oral medication if you do, in fact, truly have thrush (yeast infection). I had a doc who had been a doc for nearly 30 years. He treated me several months for something i didn't even have. You are going to want to rule out any skin condition. That can be done by having a biopsy of your skin taken and/or by seeing a dermatologist of the Vulva area. Your UK friends can help you navigate the UK system. I am usually lost when i read their stories..ha ha..not really. You should get to a vulvar specialist. also, note: gynocologist do not know how to treat women for pain. a pain clinic or family doctor can do a better job. you want a pain pill w/ opiates...if you plan to take some. i have had much success w/ the medication Neurontin and Lyrica. some of the gals there are on Amitriptyline. we all have different results with different meds. Dont' give up hope. there is a lot you can do. Some of us are doing physically therapy, nerve blocks, botox etc. you have a lot of options. But, you do need to rule out other things as well. keep in touch. you are all sounds asleep and i am getting ready to go to bed in the U.S. Good night! and Good morning to you!

jules

Posts : 225
Join date : 2010-03-17

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Post  Sarah001 Fri Sep 03, 2010 12:38 pm

Hi Cat and welcome. I'm with Julie and Sebby I'd avoid thrush creams if you can, I found they made my skin much worse. You sound alot like me thinking it might be a UTI or thrush but turning out to be neither, that's exactly how mine started and antibiotics took away a little bit of the UTI type pain but nothing else. It often starts out of nowhere.

The reason GPs don't often use the term vulvodynia is because it's not really a diagnosis as such, the word just means "pain in the vulva". If you're not happy with your GP pop along to your GU clinic and get them to examine you, they will swab for everything and probably send you away with a tube of hydrocortisone cream as a first course of action and if that doesn't work they can refer you to a dermatologist so you don't need to keep wasting time going to the GP who will keep treating for thrush when that isn't the problem (mine did that too). If you want to try hydrocortisone before you go to the GU clinic just buy some from the chemist then you can save time by having already used it. It should work in a week if it's going to.

The GU clinic can also prescribe you pain relief and if that works they can write to your doctor (with your permission) to get those medications put on repeat prescription.

If you want to try pelvic floor retraining (there's a huge link between a high resting tone of the pelvic floor and vulvar pain) it's better to ring some Women's Health Physios privately, there aren't many on the NHS so you'd wait months to see one that way and as you only need to go in once a month it isn't hugely expensive to pay for it yourself (about £35 a month). You need one that uses a biofeedback machine so they can test what your pelvic floor is doing and teach you how to get it working correctly.

If you have sore skin oestrogen treatments have worked for some women so that's another option to help the skin along but definitely do something, you're very new to the problem and the earlier it's treated the better the outcome so draw up a plan of action so you keep trying things.
Sarah001
Sarah001

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Post  Mouse Thu Sep 09, 2010 12:59 am

Hi Cat,

I'm also new and have only been on this adventure since I had surgery down there in February.

The gynaecologist who preformed my surgery had no clue what I had or what to do about it! She treated like I was a freak and left me hanging for months while I got more despondent and depressed.

Then I got mad...!!! Have you heard of the saying "And that's when the fight started". I researched and found out what I thought I had and got busy trying to find answers. Anyhoo very long story short I found a specialist in vulval pain in another city, flew there for a day (on my own ahhhh had to wear my big girl pants that day) and was diagnosed immediately. I think I love her, if it was appropriate I would have hugged her... but that would have created another awkward problem Laughing She told me most people she sees have been told they are mad at some point.

So my lovely, as other people have said find a vulval pain specialist. There should be a clinic at any major hospital. They do this thing all the time so don't be embarrassed either. Find a pain clinic also. I have a therapist who helps me make sense of this shizzer and that's really helpful as well. xx. late for work now!

Mouse

Posts : 303
Join date : 2010-09-09
Location : New Zealand

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