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Looking for a friend IRL; LA/OC

Tue Jul 18, 2017 2:51 am by crypticcalico

Hello!

I am hoping to find a friend in the LA/OC area that I can meet up with in person. I live in Long Beach, California and I am willing to drive a bit to meet. The only person that I've told about this is my doctor(s) and someone who couldn't wrap their brain around it. It would be nice to be able to talk to someone else who understands.

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Constant pain, I want to die.

Fri Jun 02, 2017 4:29 am by Meggiemay

I posted on here a few years ago but my symptoms went away with the inflammation. I didn't get so lucky this time.

For over three months, i've had terrible rawness, burning, soreness in the urethral/vestibule area and pressure/hypersensitivity in the clitoral area. I've also had some lower abdominal pressure and burning on my butt. I can barely walk! My gyno hasn't been much help. I'm on …

Comments: 20

Owner of vulvodyniSuppoet.com

Wed Jul 19, 2017 10:28 pm by LaurenVV

Hi, I started vulvodyniasupport.com at the age of 28.
I was a leader when there was no help, no forums etc.

As I went on my path, I found acupuncture, herbs and time helped me recover.
Most never do.

I met a wonderful woman named Hanna. She was a patient and became a support leader. She lived in FLoroda.

I have moved on from the support world and found a career that allowed
Me to bring my …

Comments: 0

anyone from southern california in here?

Tue Jul 12, 2011 6:43 pm by Melissa777

Hi Im just wondering if anyone here is from so cal- USA
I am in san diego- but from LA!!!

Comments: 6

Anyone else try Cold Laser therapy/ Low Level Laser Therapy for their vestibulodynia?

Tue Jul 04, 2017 9:01 am by Tired89

Hello everyone. It's been quite a long time since I've posted. I've been extremely depressed and bottling it all up. I've been seeing a pelvic floor therapist (it's only been 4 visits) for my provoked vestibulodynia and the only reason she can get inside of me to do myofascial release and to use the dilators is because I use BLT (benzocaine, lidocaine, tetracaine) ointment on my vestibule prior …

Comments: 2

Clitoris Issues

Tue Apr 28, 2015 8:17 pm by January

I am going crazyyy trying to figure out what's wrong. Please does anyone else have an issue similar to mine? I'm only 22. So, basically when my clit is lightly rubbed, there is no feeling. However, when rubbed vigorously and directly, the burning and tingling sensations shoot down my legs and feet as if coming to the end of an orgasm but with no good feeling leading up. It's so strange. What …

Comments: 1

New member

Sat Mar 18, 2017 7:37 pm by Lisa1627

Hi ladies. I am new to the forum. I have had what I think is vulvodynia caused from hsv 2. So not only do I have the burning vag but the constant feeling of being contagious. I can honestly say that I hate my life and myself right now. There are days when I think I would rather be dead. I tried the amitryptline and it helped but if it's only making my brain think I don't have pain then it's …

Comments: 12

Post Full Vestibulectomy - 5 Years Later - Please Read

Tue May 02, 2017 6:18 pm by jen007

Hi All,

It's been awhile since I've written a new topic on the forum. Wondering if any of the same ladies are still here. I've come back to update you all on my post vestibulectomy results. I can't remember if I've done an update on my current state, so forgive me if this is repeated information... I can't remember how to view my old posts! Anyway, let me get on with my update.

For 4 years post …

Comments: 3

Recovered from Vulvodynia

Thu May 04, 2017 9:42 pm by chancesunny

Hey everyone,

Im a new member on this forum and wanted to share my story so I can help anyone who is feeling helpless. Maybe what worked for me can work for you. I'll try to make this short so you can go get better!

I had vulvodynia for about 3-4 years. In the beginning, it started with pain that I thought was just a yeast infection and then I thought it was a urinary tract infection or …

Comments: 2


Forum now optimized for viewing on your mobile!

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Forum now optimized for viewing on your mobile!

Post  Sebby (Admin) on Sun Feb 27, 2011 12:03 am


Forumotion have now enabled the forum to be optimized for veiwing on your smart phone (andriod, blackberry, Iphone etc)

Its still in process so you can view all posts just not post yourself yet..will anounce as soon as posting is enabled

I have just tried it on my andriod phone and it looks great Smile can't wait for the posting to be enabled


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Re: Forum now optimized for viewing on your mobile!

Post  naomi on Sun Feb 27, 2011 10:59 am

you're a technical whizzkid!!
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Re: Forum now optimized for viewing on your mobile!

Post  Sebby (Admin) on Sun Feb 27, 2011 3:17 pm


Wish I could take the credit! its forumotion, they messaged me in the admin panel bout it..I looks cool on the mobile tho.

I am looking to getting my own domain name for the forum, doesnt cost much per year like a tenner I think..better check that out.

Think it would look more professional to have the address as www.vulvodyniasupportforum.com or net or whatever I can get..People will still be able to access it under the old address..Im wondering now if I can get rid of the Forumotion.com at the top and make the actual forum name bigger.

I may also disable the adds as they get on my nerves and hopefully I should be able to add my own links to the websites I actually want to advertise..

For some reason Google keeps adversting stuff about eating disorders! as well as advertising bloody money grapping sites that I just dont trust

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Re: Forum now optimized for viewing on your mobile!

Post  Sarah001 on Mon Feb 28, 2011 7:57 pm

If you buy a domain name Sebby try 123reg.co.uk they are very reasonable but make sure you opt out of the "who is" section or your name, address and vulvar history will be available for all to see!!
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Re: Forum now optimized for viewing on your mobile!

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