How I cured my vulvodynia

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I see so many posts on here about constant or provoked vulva pain that I thought it might be useful if I explained vulvodynia and how I cured mine. Vulvodynia literally means vulvar pain and is a condition of the nerves in that area. The nerves have become hyperactive and hypersensitive due to trauma which can be chemical or physical in source or due to infection. I think mine was due to persistent thrush infection and the many remedies I tried to cure it, including home remedies such as bathing in a bath with some cider vinegar in - that made my soreness much worse (chemical trauma). Vulvodynia can cause itching, sore or burning sensation and this can be continuous or provoked (only happens when the area is touched). The nerves are so hypersensitive they register touch as pain and the usual way to diagnose it is to touch around the vulvar area with a cotton bud and where the touch registers as pain then that is the affected area. It can involve the whole of the vulvar area or can be in a horseshoe shape toward the posterior (which may also involve the perineum) or the anterior or can be offset to one side. The pain is a form of chronic neuropathic pain because it stems from nerve damage as opposed to nociceptive pain which is caused by tissue damage. Neuropathic pain can be very hard to get rid of. It took me 1.5 years of determination and the occasional disappointing set back to cure my vulvodynia. Probably more like 2 years to get back to normal.

Ok, ready for a long story about how I cured my vulvodynia:-

First I saw a gynaecologist. He took a biopsy of the painful area and confirmed no diseases or cancer. He put me on amitriptyline and steroid cream. These slowly worked for a while and made me comfortable enough to have a long overdue smear test. I had the smear test and the pain came back full force - back to square 1. By that time I had used the steroid cream for as long as is recommended and had stopped it (long term use not recommended). However, desperate to get rid of the pain I tired it again, but this time the cream stung me and made the pain worse. The gynaecologist gave me lynocaine cream to numb the area, but that stung me and made me worse. Nothing was working and in the end the gynae said that he could not cure me he could just help me managed the pain. Well, I wasn't going to put up with that for the rest of my life. So I did some investigating to find someone else who could help me and found a dermatologist consultant in Oxford who specialised in vulva pain. I also found some medication on the internet, made in Italy which is a gel is specifically for treating vulvodynia. It calms down the overactive and hypersensitive nerves. Saginil gel  - you can order it direct from the suppliers, epitech, on their website. You can do this because it is not classed as a medicine because it is made of natural plant-based ingredients. It is expensive, as is the post from Italy, but I am so pleased I bought it because it was the only thing my skin could tolerate there and it did make a difference - it reduced the pain so that it was bearable and I could function better with daily life.

i saw the dermatologist and she told me all the things that she had found worked to get rid of the pain, but nerve pain is difficult to get rid of so she suggested I try them all and stick at it. i was surprised because, appears from upping the amitriptyline dose to 50-70mg a day (I was on 20), the rest of the things were what you would class alternative, or natural, cures. They were: western acupuncture, physiotherapy, chiropraction and manual desensitisation. Now, different things work for different people because there are different causes for the vulvodynia: infection, physical or chemical trauma, hormones, trapped nerve in back. I knew mine was caused by repeated and persistent thrush and the various treatments I tried to get rid of it (including cider vinegar - ouch! No!). So I didn't see a chiropractor because is didn't thing it stemmed from a pelvic nerve problem, however, from what you describe, yours might. I did do yoga exercises that free trapped pelvic nerves. I bought a book on pelvic floor exercises and did those, rather than see a physio. I did the manual desensitisation - this is where you stroke yourself very lightly in the painful area, using non-irritating lubricant (I used oil based lube by yes, or coconut oil), just once the first day. Then each day you gradually build up the strokes in number and pressure. The idea is that you are retraining the nerves to register touch as touch and not pain. So, massage yourself there just enough so as not to cause lasting pain afterwards. I built it up until I could do 100 strokes of fairly good pressure, then I moved into inserting a finger, then two, then the tip of my husband's penis and then gradually out him in a little further each time, until I could get most of him in, then starting moving with him in, again gradually building it up each time. I also found a GP that also ran a Western acupuncture clinic. Western means that they leave the meddles in and pass electricity through them. That was what really worked for me - each time I went I just got better and better. Apparently the amitriptyline and the acupuncture work well together to dampen down those hyperactive and oversensitive nerves. I upped the amitriptyline to 50mg as day, very gradually by 5mg every 1 or 2 weeks because it caused side effects so my body needed to adapt to each increase. 

Finally, there are the changes to how you live. No tight clothes, no sex (until you are ready), no exercise (I gradually built that up too but walking just a short distance and gradually increasing it - never do an amount that cause she lasting pain). Go knicker free if you can - I work mainly from home so was able to go around with no knickers on and baggy jogging bottoms or a skirt. Sitting also caused problems (I work at a computer) so I got a ring shoved cushion form woman to use after they have given birth and sat in that so that there was no pressure at all on the sensitive area (dame for driving the car). Coconut oil was soothing (raw, cold pressed, organic coconut oil) so I applied that externally and internally with a clean finger after every time I went to the loo (I carried a little pot in my hand bag so I could apply it while out and about with an organic, pesticide and bleach free cotton pad). No scented products on that area, in fact I didn't wash there at all, I used coconut oil to clean the area and when showered I used organic, nasty chemical free and scent free body wash and shampoo and conditioner (because stuff runs down). I also washed my clothes in scent free, kind-to-skin laundry detergent and conditioner. Toilet paper has bleach in it, so I got some tissues that were bleach free and used those to wipe after doing a wee.

The key is to be persistent, try everything, gradually build things up, stick with what works, be determined, don't give in. The consultant dermatologist was very impressed with me because I was so determined and didn't give into urges. She said she had many women who just got fed up with how long it was taking and just went for a long walk / bike ride / horse ride or had sex and put themselves back at square one again. It does take a long time - it took me 1.5 years of all that stuff in my message above to get to being pain free. Even now, 5 years later, I still apply coconut oil after every time I go to the toilet, use tonnes of oil based lube during intercourse, go around the house wear no knickers. I don't want it to come back. I am also still on 50mg amitriptyline a day. At first I was afraid to come off it because the consultant dermatologist told me, you may be pain free, but if you come off it too soon, the pain can come back. So it is best to wait a few months after being pain free. Then menopause set in and I got hot flushes and my GP told me to stay on the  amitriptyline because it helps with hot flushes. My body has adapted to it now. I hope to reduce the dose sometime (gradually, by 5mg very 2 weeks, just like I built it up). I still do pelvic floor exercises - the book I got was called 7 steps to pain-free sex by Claudia Amherd. It is mainly about vaginismus, but the exercises apply to vulvodynia too - just don't do them sitting on a juggling ball (ouch) do them standing up first, then lying down, as it advises in the book. Gradually build up the exercises, doing more and more each time. Again, don't do so much that it causes an increase in pain or lasting pain - cut back if that happens.

Also, you need to get some organic, chemical free sanitary towels for when you have your period (no tampons). 

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  • Posted

    Hi Suki,

    This has been so interesting to read. I have had unprovoked vulvodynia for over 4years, I have seen a Woman’s Health Physio, Osteopath, Deep Tissue Massage, Vulval pain  Dermatologist and I am now having acupuncture and Gua sha, I have just had my 5th session and have seen some improvement all though not as much as I would like to have. I am wondering how many acupuncture’s you have had? and if you have reduced your amitriptyline yet? , I took this in the early days and did not get on with it, I then took Gabapentin which I stopped taking 1 month ago and I am finding that I have more good days than bad which is good. I find myself getting really impatient and I just wish there was more knowledge of this condition in the medical world. 

    • Posted

      Four years 🙈🙈 sorry to hear that. I am seeing a physio and getting better. What did physio say to you was ur pelvic floor the cause of ur symptoms?

    • Posted

      She said I had some knots in my pelvic floor which she did massage on and gave me stretches.  I was having tingling/prickling In my lower back, hips and tops of legs too so she wrote to my Gp asking him to refer me for an MRI as she thought it might be something to do with my back, which he refused to do. Bad I know! I then went to see an osteopath who found my pelvis was out of line and a disc bulge. He corrected my pelvis and relieved the disc bulge which helped a little. Although he did say it takes a while for the nerves to recover. There is no more he can do for me which is why I started acupuncture and I am going back to the Gp on Tuesday to ask again for an MRI as I feel like I’ve spent enough of my own money now and it’s time for them to give me something back. Hope it goes well with your physio. I might even see them again in the future 
    • Posted

      HI Katie. Nerves do take a long time to heal. I fell from a kitchen surface I was standing on while painting the kitchen wall and landed on my knees on the hard floor. The next day I couldn’t raise my right leg without shooting pains down my leg. My foot gave me so much pain in the night that I couldn’t sleep. An MRI showed no disc damage in my back so the consultant thought that when I landed my vertebrae had slammed together and brushed the nerve. It took around a year of physio to be pain free.

      Anyway, back to vulvodynia. My acupuncturist told me I’d need 10 sessions every 2 weeks. I had the 10 and then gradually increased the time between sessions to a month, then stopped. I can’t remember exactly how many I had but it was a few over the 10. It might be worth trying amitriptyline or nortriptyline or sinething similar too as it can work in unison with the acupuncture to heal the nerves.

    • Posted

      Hi Suki,

      Thank you for your reply. Gosh a Year is a long time for them to heal isn’t it. Re the acupuncture I have had 5 now the lady thinks I should have 2 more and then she will review it, I have been going every week and have noticed gradual improvement and seem to have more good days than bad now which is good compared to how I was a year ago.  I will consider going monthly when my weekly treatments have finished and I will consider the amitriptyline again. I really hope that one day some proper research will be done and an easy cure will be found a I am sure their are more women out there with this condition than what is documented. I hope remain well and thank you again for sharing your remedies.

    • Posted

      Hi again Suki,

      I have started wearing looser clothes too as I was reluctant to giving up my jeans. Do you think by wearing looser clothes gives the nerves better chance of healing? 

    • Posted

      The reason there is no cure is because the word vulvodynia just means pain in the vulva so its the same as headache. Unless you treat the cause or whatever is keeping the condition going there is no one size fits all treatment. For one person it might be allergy reasons for another it might be hormones for another it might b muscles for another it might be overactive nerves after an infection that needs to calm down. So its just trial and error. A multimodal approach I guess. Physio for me is turning out to be whats helping as she identified its the tight muscles in my pelvic floor and all over pelvs tthat is compressing the nerves. Came after an infection and years of anxiety. Amitryptaline is also helping it along.
    • Posted

      Looser clothes are a must. Anything pressing on those nerves will aggravate them. But I can assure you that it will not be forever. I can wear shimmy jeans now. Still wear loose clothes and no knickers around the house though.
    • Posted

      I have read an estimate of 13% of women living in the USA have vulvodynia at some time in their lives.
    • Posted

      That's a high percentage.  Most people and friends I have told of my condition have never heard of it.  I suspect women just don't talk about it, probably through embarrassment.  Must admit I too has never heard of it until November.  I agree loose clothing does help.  I can't wear my jeans any longer either, but just wear leggings or skirts.  I find also that panti liners aggravate it too, so just wear knickers that get wet with all the creams and Vagifem I use but that's a small price to pay, just keep changing several times a day.

    • Posted

      That’s good to know. I love wearing my PJ’s when I’m at home but I will definitely leave the jeans out for now. 
    • Posted

      I agree most women probably just suffer and don’t talk about it. I feel very sorry for those who do not have access to all the resources that We do that can help.

      If I had to go out I’d wear underpants but with all the oils I used the oil would soak through. Just took care not to wear any materials that the oil showed through. Oil stains don’t wash out with the skin-kind, nasty chemicals free, unscented laundry liquid and conditioner I use.

  • Posted

    A couple of my friends told me about their problems with vulvodynia after I told them about mine.  Two other ladies got total relief from changing their diet, one was like me sensitive to solanacea, while the other lady got her GP to do a skin allergy test and it turns out she couldn't eat citrus without getting problems. The acid in citrus (and tomatoes) was what set hers off each time. 

    I look back at the days when I was trying desperately to find a cure without knowing the cause, and shudder.  I never have any problem with it now that I no longer eat my trigger foods.  

    Minamii

    • Posted

      I’m so pleased you found your cure. Because I am vegan I eat a lot of tomatoes and peppers and fruit. It seems that foods were not my cause. But it is interesting that a food allergy can cause vulvodynia and I now add that to my list of causes when I am telling people about vulvodynia.

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