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Vulvodynia

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Hi I am new to this site, I have been suffering with vulvodynia for

over a year now, it gets so bad that I have to sit on ice and take some

Darvocet, I just started taking Neurontin and I have not felt any

difference yet can any one tell me if they had any luck with Neurontin

and how long it takes to work, I am sooo depressed about this some days

I just lay on the couch and cry....so please any advice would be

greatly appreciated...thanks Jen

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Jen, many of us have cried many tears...but please know that there is HOPE! What are your symptoms and what have you used for help besides Ice and pain meds? I encourage you to look through our files, links and database on the homepage when you feel up to it. Hang in there and Welcome to the group! ;) ~Chelle

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>

> Jen, many of us have cried many tears...but please know that there

is HOPE!

>

> What are your symptoms and what have you used for help besides

Ice and pain meds? I encourage you to look through our files, links

and database on the homepage when you feel up to it.

>

> Hang in there and Welcome to the group! ;) ~Chelle

>

Hi Chelle, Thanks for responding, I have been taking Neurontin I am

finally up to a 1000 mg for about 2 days now with no improvement, I

am not sure how long before you see any improvement,I also tried

premarin cream but seemed to make things worst so I stopped... my

symptoms are mostly burning in the vestibule area but are now

spreading out to my outer labia and sometime my ananl area, so I am

convinced I have some sort of nerve damgage, I was diagnosed with

Lichen simplex chronicus 2 years ago but that has pretty much under

control but I think that and that recurring yeast infections that use

to have before I changed my diet caused my vulvodynia, I jsut want

some improvement right now it is even hard to sit without pain it is

very discouraging........Thank you so much , Jen

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If you had LS at one time – you still may not have any visible

symptoms, but LS does just cause pain. I use a dab of CLBOB twice a week just

for pain (I have LS also), and I also use 5% Lidocaine gel twice a day. If you

have any anti-anxiety meds like valium, that also might help.

nne

From: VulvarDisorders

[mailto:VulvarDisorders ] On Behalf Of jen9952

Sent: Saturday, May 10, 2008 7:06 PM

To: VulvarDisorders

Subject: Re: Vulvodynia

>

> Jen, many of us have cried many tears...but please know that there

is HOPE!

>

> What are your symptoms and what have you used for help besides

Ice and pain meds? I encourage you to look through our files, links

and database on the homepage when you feel up to it.

>

> Hang in there and Welcome to the group! ;) ~Chelle

>

Hi Chelle, Thanks for responding, I have been taking Neurontin I am

finally up to a 1000 mg for about 2 days now with no improvement, I

am not sure how long before you see any improvement,I also tried

premarin cream but seemed to make things worst so I stopped... my

symptoms are mostly burning in the vestibule area but are now

spreading out to my outer labia and sometime my ananl area, so I am

convinced I have some sort of nerve damgage, I was diagnosed with

Lichen simplex chronicus 2 years ago but that has pretty much under

control but I think that and that recurring yeast infections that use

to have before I changed my diet caused my vulvodynia, I jsut want

some improvement right now it is even hard to sit without pain it is

very discouraging........Thank you so much , Jen

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nne, I had lichen simplex chronicus that is a form of

dermatitis, I do use Clobetasol 2x a week but the Lichen simplex was

in one tiny area, now the pain is all over even on the labia majora,

I guess it could be caused by the lichen simplex, but the doctor

seems to think it is nerve damage, I have heard that Lyrica works

better than Neorontin but I am not sure, have you ever tried

Lyrica??? and I would really like to now what kind of shots you

recieve??? is it cortisone?? I will try anything to get this under

control.....

Thnak you so very much

Jen

> >

> > Jen, many of us have cried many tears...but please know that

there

> is HOPE!

> >

> > What are your symptoms and what have you used for help besides

> Ice and pain meds? I encourage you to look through our files, links

> and database on the homepage when you feel up to it.

> >

> > Hang in there and Welcome to the group! ;) ~Chelle

> >

> Hi Chelle, Thanks for responding, I have been taking Neurontin I am

> finally up to a 1000 mg for about 2 days now with no improvement, I

> am not sure how long before you see any improvement,I also tried

> premarin cream but seemed to make things worst so I stopped... my

> symptoms are mostly burning in the vestibule area but are now

> spreading out to my outer labia and sometime my ananl area, so I am

> convinced I have some sort of nerve damgage, I was diagnosed with

> Lichen simplex chronicus 2 years ago but that has pretty much under

> control but I think that and that recurring yeast infections that

use

> to have before I changed my diet caused my vulvodynia, I jsut want

> some improvement right now it is even hard to sit without pain it

is

> very discouraging........Thank you so much , Jen

>

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Jen... just a thought...

The steroids esp. the Clob is a class one in potency.. extremely strong... and believe me overuse of that can destroy or fry those nerves too and of course it doesn't stay just where you apply it, it seeps. (Went up to my tail bone to give me blisters there it was so bad, I'm a back sleeper.).

So it's just a thought hon and I've no idea for how long you've used it.. and would agree that twice a week doesn't seem like much... but it depends on how long (say if it's been 6 months?) 'I'd' surely give it a second thought that it might be that. For what it's worth hon.

Also have you added the Estrace or estradiol? Believe me there's nothing better to restore that tissue than that, esp. with lichen simplex as it is for any V pain if the issue is the tissue & damage there.

hugsDee

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>

> Hi Dee, I have been using the Clobetasol well over a year and it

worked great for the first 6 months or so now I have pain not just in

the vestibule but all over even on my labia majora.

M doctor did prescribed estrace cream but my insurance would not

cover it so I got premarin cream, but she told me to insert it up in

the vagina for 2 weeks then 2x a week, but it did burn and made my

labia majora inflammed, I have no idea why...but hat is my luck so I

havent used it since..

So how often do you apply the estrace cream to the inflammed tissue??

and how long before yoy see results???

Thank you very much

Jen

>

> Jen... just a thought...

>

> The steroids esp. the Clob is a class one in potency.. extremely

strong... and believe me overuse of that can destroy or fry those

nerves too and of course it doesn't stay just where you apply it, it

seeps. (Went up to my tail bone to give me blisters there it was so

bad, I'm a back sleeper.).

>

> So it's just a thought hon and I've no idea for how long you've

used it.. and would agree that twice a week doesn't seem like much...

but it depends on how long (say if it's been 6 months?) 'I'd' surely

give it a second thought that it might be that. For what it's worth

hon.

>

> Also have you added the Estrace or estradiol? Believe me there's

nothing better to restore that tissue than that, esp. with lichen

simplex as it is for any V pain if the issue is the tissue & damage

there.

>

> hugs

> Dee

>

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