Log in

I forgot my password

Latest topics
» Can you guys tell me your experiences with diflucan/Fluconazole?
Today at 1:29 am by ryn207

» So frustrating!!
Today at 1:25 am by ryn207

» Looking for suggestions or encouragement
Today at 1:19 am by ryn207

» Looking for a friend..... and new problems
Yesterday at 10:00 pm by VVSSufferer

» Vestibulectomy recovery question!
Sun Jan 14, 2018 11:37 pm by Kezz

» Prescription creams that work!
Sun Jan 14, 2018 4:46 am by Mintaherb

» Struggling
Sun Jan 14, 2018 4:29 am by Mintaherb

» Went Away and Came Back
Sat Jan 13, 2018 10:56 am by mary jane

» Amitriptyline given for vulvodyina pain
Sat Jan 13, 2018 1:39 am by ryn207

So frustrating!!

Thu Jan 04, 2018 1:15 am by Hannah77

Well I'm back in pain after 7 years of pain free days.
I was diagnosed with vulvodynia when I was 17. I suffered for three years with horrible burning all day, painful sex with my boyfriend and just pure misery Sad I went into a spontaneous remission when I was 20. I'm still not sure how the pain stopped but all the sudden I could go an entire day without thinking of my vagina, sex started to …

Comments: 3

Looking for suggestions or encouragement

Sat Jan 13, 2018 12:10 am by ryn207

Hi there. I'm 25 and have been dealing with this for over a year and a half and I'm really starting to lose hope this will ever stop.

In July of 2016 I had a yeast infection. When Monistat didn't work I went to my gynecologist who prescribed Diflucan. When the itching didn't stop she retested me and found that my yeast infection was gone, but I now had a bacterial infection. After taking the …

Comments: 4

Looking for a friend..... and new problems

Sat Jan 06, 2018 11:38 pm by infinitelywondering

Hi everyone,

I hope you're doing well.

I hate to say this, but I feel beaten down and terribly alone. I had a vestibulectomy surgery about 6 months ago and I was absolutely praying it would work. It didn't.

6 months later and here I am, sitting on my bedroom floor crying my eyes out because I know I'll never be able to have painfree sex. I don't know what to do and just need a friend Sad



Comments: 5

Amitriptyline given for vulvodyina pain

Tue Oct 24, 2017 2:46 pm by katycrawford

Hi there,

After years of being misdiagnosed etc as most women have on this forum I have finally been diagnosed with vulvodynia (yay) and have been given the lowest dose of an antidepressant called Amitriptyline. Has anyone been on this before and has any positive (or negative) news to give me? Im feeling down already and I've only been taking it for a few days, I don't have much hope of it …

Comments: 11

7 years later and life looks bleak :(

Wed Dec 06, 2017 2:50 am by RainyShay77

So 7 years ago I had a case of BV...the antibiotic caused a horrible yeast infection which took 5 months to 'get rid of'. During this time I had allergic reactions to 2 of the yeast infection creams which magnified the pain. Over the past 7 years I've tried multiple rounds of physical therapy (they only slightly helped), chiropractic, nerve blocks, medications to target nerve pain (amitriptyline, …

Comments: 7

Newly diagnosed - and prescribed amitriptyline cream/physio/psychology

Sun Jan 07, 2018 9:38 am by sophiarp

Hi everyone,

I'm so happy to have stumbled across this forum. I have just been diagnosed and am really struggling emotionally. It's nice to find this forum and feel a little less alone.

I've been prescribed amitriptyline cream. Has anyone had success with this? I was happy to have avoided the amitriptyline tablets. I'm also participating in physio and have been told I need to see a psychologist …

Comments: 2

Somebody please help me...

Fri Nov 24, 2017 8:05 am by Andlag

Hey everyone,

since I started being sexually active i often experienced burning in my vagina which was often worse during sex /around the time of my period or when using lubricants. I was never able to use tampons because the one time i tried putting them in it felt like acid was poured on my skin. Fast forward to 2 months ago when I got a UTI and an allergic reaction in my vagina. I thought it …

Comments: 11

Amtriptyline, baclofen, gabapentin cream for provoked vestibuldynia

Mon Nov 20, 2017 8:15 pm by WVR00

Hello,
Has anyone had success with this cream in helping their vulvodynia? How long has it taken to help? I’ve had some success with it, but not completely better. I’ve been on it for a month. I️ was hoping to hear from some ladies who have had major success with this cream. I’m hoping for some encouragement here. This condition is so frustrating. I’m lucky enough to have access to two …

Comments: 1

New diagnosis, any advice whilst I wait for a specialist

Wed Oct 25, 2017 1:47 pm by Julesyjules

Hi,

I'm new here and wanted to ask for some advice whilst I wait to see a specialist nurse.

After urinary problems which lasted 7 weeks, I finally saw a urologist, who on examination discovered significant inflammation and called in a gynaecologist, who diagnosed vestibulitis. They referred me to a nurse who specialises in vulvar skin issues. That was 5 weeks ago, and I'm still waiting for the …

Comments: 1


Interesting study

View previous topic View next topic Go down

Interesting study

Post  mary jane on Sat Jun 03, 2017 2:16 pm

I found this study .... I am thinking more and more that V is a brain "malfunction" of some sort, like a shortcircuit or "error" ...

"The researchers tested 17 women with vulvodynia and 23 similar women without pain at 23 sites throughout the vulva and at the deltoid muscle, the shin and the thumbnail to assess pain tolerance. They found the women with vulvodynia had lower tolerance at all sites than the women without vulvodynia.

“Vulvodynia used to be considered a psychological problem or a sexual disorder, and was not treated as a medical problem. Now we know vulvodynia is likely a neuropathic disorder in which the nerves in the area are hypersensitive. We found women with vulvodynia were hypersensitive at the vulva, not only in areas that were clinically tender, but in surrounding areas as well, and at areas not thought to be tender at all – the deltoid, shins and thumb. This study shows there are neurological differences that are not psychosomatic,” says study author Barbara D. Reed, M.D., professor of family medicine at the U-M Medical School.

Vulvodynia causes chronic and potentially severe pain at the outer genital region, or vulva. Currently, few doctors are familiar with vulvar pain disorders, and many women with intense pain are misdiagnosed for years with chronic yeast infections or psychological problems. Women with more mild pain or whose pain comes and goes often think some degree of pain in that area is normal and don’t tell their doctors about it.

In this study, the researchers used a specially designed air-spring device that attaches to a cotton swab to apply a range of pressure to the vulva and nearby areas. This device, a vulvodolorimeter, was designed by the researchers for this study so that varying pressures could be applied at different angles. The Q-tip test used to diagnose vulvodynia did not cause pressure severe enough at the thighs for any woman to rate as painful, but the vulvodolorimeter allowed researchers to apply enough pressure to determine a pain threshold for most women."

Overall increased pain sensitivity has been linked to other pain syndromes such as tension headaches, temporomandibular disorder (TMJ) and low back pain, suggesting a generalized and central underlying cause. The researchers suggest the local irritation in vulvodynia may cause neurological changes that alter the body’s central pain processing, resulting in hypersensitivity to pain throughout the body. Another possibility is that these women have widespread tenderness that predisposes them to vulvodynia.

The idea of a central cause of the pain suggests treatment should be aimed at the entire body, not just the vulvar region – for example, antidepressants, aerobic exercise or cognitive behavioral therapy.

The researchers have applied for a grant to further study sensory processing among women with vulvodynia, including their responses to heat or cold and their brain activity.

“This improved understanding of the neuropathic changes present in women with vulvodynia will allow us to better design studies to treat and manage this disorder,” Reed says. “It will also provide women with vulvodynia the information they need to better understand what is happening in their nervous system, and to know that this is an authentic, treatable disorder.”

The study was funded from the National Institutes of Health and the U.S. Army. In addition to Reed, study authors were Hope Haefner, M.D., associate professor of obstetrics and gynecology; Daniel Clauw, M.D., professor of rheumatology; Richard Gracely, Ph.D., professor of rheumatology and neurology; and Jutta Giesecke, M.D., and Thorsten Giesecke, M.D., research fellows. "


source: http://www.news-medical.net/news/2004/07/13/3295.aspx
avatar
mary jane

Posts : 328
Join date : 2013-10-05
Location : UK

View user profile

Back to top Go down

View previous topic View next topic Back to top

- Similar topics

 
Permissions in this forum:
You cannot reply to topics in this forum