Vulvodynia Support
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» Hope to all my suffering ladies
Physiotherapy and Botox EmptyFri Oct 23, 2020 12:04 am by ringostarr26

» Please tell me this can get better
Physiotherapy and Botox EmptySat Jul 18, 2020 7:38 pm by sammykramer

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

» How I cured my Vulvodynia!
Physiotherapy and Botox EmptySat Dec 07, 2019 11:54 am by Millie

» 7 months since the diagnosis
Physiotherapy and Botox EmptyWed Aug 14, 2019 2:38 am by agtoronto

» Gabapentin Gel. or other topical creams
Physiotherapy and Botox EmptySat Jun 15, 2019 5:22 pm by mary jane

» IMPORTANT FOR UK SUFFERERS
Physiotherapy and Botox EmptySat Jun 15, 2019 5:21 pm by mary jane

» Help New Diagnosis
Physiotherapy and Botox 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!
Physiotherapy and Botox 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


Physiotherapy and Botox

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Post  cba321 Wed Oct 03, 2012 12:29 pm

I have always had vulvadynia since starting to have sex. Pain is usually only present with touch or penetration. Have tried various treatments such as biofeedback, psychotherapy, Endep medication, low oxalate diet, antifungal medication and had various tests including thin prep (multiple and all clear), blood tests (no STDs) ultrasounds (all clear) and an MRI (all fine except prominent vascularlity along the pudendal nerve and bulky pelvic floor muscles on the right side even post botox).

Two months ago I had botox injections to my pelvic floor muscles and am doing 30 minutes of exercises with dilatators every day and seeing the Physiotherapist every three weeks. Botox has worked very well, for the first time I can actually stretch the muscle and give me some form of fighting chance to stretch the muscle out before the botox wears off in the next few months, in the hope that the muscle retains some of the stretch

I have recently confided in a few friends but they offer limited to no support, I don't think they understand how damaging this is to my self esteem and my potential relationship future. I haven't entered into a relationship in a long time, because I just can't handle the stress of it all.

Has anyone done Botox with exercises? I'm getting to the larger sized dilatators and the pain is returning somewhat, it was almost totally absent with the smaller dilatators. Previous to Botox the pain was INSANE, even with the smallest dilator.




cba321

Posts : 69
Join date : 2012-07-14

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Post  Rose86 Thu Mar 21, 2013 10:06 am

Hi! I was wondering if you had any success with the botox? Did you have localised provoked VV? I do and I'm considering trying it. Thanks!

Rose86

Posts : 51
Join date : 2011-06-23

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Post  cba321 Thu Mar 21, 2013 12:15 pm

Hi,

Yes I have provoked localised V, I am coming up to 8ish months post botox and I can use the largest dialator with no muscle pain now but I believe the botox is still working on my muscle. Currently I am only left with the neuropathic pain/sensitivity around the vulva and burning. The true test will be when it has worn off and if the muscle can still remain stretched. You need to do a lot of stretches and daily, so it is hard work and expensive! For the moment it has been worth it. Botox doesn't work for everyone and also depends on the skill of the person injecting you on how it will work. I also see a chiro, general physio on top of a pelvic physio, light touch myofacsial massage, exercise physiologist for specific exercises to normalise both sides of body and psychologist - trying to give my poor pelvic floor muscles a better home to go to when they are eventually revived after botox Razz


cba321

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