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 did you try dialators. Have been reading up on this and seems could help.

    Thanks

    • Posted

      yes, I used those but only once I had gone through the manual desensitisation process. Then I used them to prepare myself for sex.

  • Posted

    Hi @Suki_girl, thanks for sharing your experience. I have had vulvodynia for 14 years and have tried many of the same things you have but I've not managed to be as persistent! I actually wanted to ask you about the persistent thrush you mentioned. I have had thrush for 5 months now and its driving me nuts and really aggravating the vulvodynia. How did you get rid of yours in the end?

    Thanks

    Laura

    • Edited

      I did the special diet (i can name it because they will delete my post) - no sugar or carbs at all for 2 weeks, then gradually reintroducing natural sugars (fruit) but never eating added sugar for years. I also took anti-fungal suppliments e.g garlic, pre and pro biotics, caprylic acid, rosemary, thyme, oregano oil extract, etc. the frequency of infections gradually decreased (every 4 months, then every 6, then every 12, etc, until i haven't had it for years). It is important to stop the infections because those will aggravate the vulvodynia.

    • Posted

      Thanks very much for the info. I think I will try the diet. Were you on antifungal medication at the same time? I'm on Itraconazole at the moment and I'm also taking probiotics.

      Thanks again,

      Laura

    • Posted

      No, the anti-fungals either weren't working or the thrush had gone and turned into vulvodynia. So, I just did the diet and supplements for a long time. The dermatologist I saw told me that if I did get thrush again I had to take 100mg fluconazole every day for a week and that did seem to work on the odd occasion I did get it (usually when I got too hot).

    • Posted

      Ok, I'll see how I get on with the diet and the supplements. Thanks so much for your help.

      Laura

  • Posted

    hi all just wanted to share that during lock down and the stress of it has seen my Vulvadynia re emerge after nearly a year clear . i started taking ibuprofen every 4 hours and using lidocaine every 4 hours . After a few days it went away so i stopped using them . it came straight back . ive restarted and am finding that most of the day im pain free . some days when i get close to the next dose it gets uncomfortable but soon as i take the doses it settles back down . ive been able to walk every day to help my mental health and whilst i dont want to use the medication its working

  • Posted

    Hi, everyone! New things happened in my life so i wanted to tell you about it! Till now i went to 3 well- known doctors from a big city for my vulva pain (i sense pain at the slightest touch), but 2 of them knew nothing about vulvodynia and 1 one them told me vulvodynia means pain only when you're trying to have sex. Five months have passed since my last gyneacological exam and a week ago i decided to go to another doctor from a small city because there was something strange with my vaginal discharge. My test results showed that i have candida and klebsiella caused by my chronic constipation. Since i was there with her talking about my treatment, i asked her about my vulvar pain, if it could be vulvodynia and i was shock to hear that she knew what vulvodynia is and that's what i have but she won't give me a treatment for it until i don't treat my infection. She told me that candida and klebsiella can cause vulvodynia, that those infection led to my vulvar pain. Now i'm waiting for my menstruation to pass to start my treatment and hopefully this new doctor can help me. I'm a bit worried because when i asked her if it's difficult to treat vulvodynia she said "no", but so many women have problems with this condition that i don't know what to think anymore. And there is another problem, that every time i'm taking medication for something my problem with constipation is getting worse, even antibiotics are causing me severe constipation. I really don't know what to do anymore, i just want to wake up from this nightmare.

  • Posted

    just read this as starting my journey with vulvodynia. its such wonderful advise. I was a bit sceptical of using amitriptyline but a physio i saw last week encouraged me and reading this has made me feel positive. My dermatologist said to use instigell which is licodaine based so will give that a go. I have noted you used something else from Italy. Its good to hear there is light at the end of the tunnel with persistance. Think mine started with thrush too. Im saving this as such great advise x

    • Posted

      Thank you. I am still pain free. Do take amitriptyline and I really recommend western acupuncture and manual desensitisation. These things work together in damping down the over activity and over sensitivity of the nerves that have been traumatised by the thrush. The saginil gel I used contains natural plant derived ingredients which work against the inflammation of the tissues in that area. The repeated thrush infection has also caused the body to overdo it's natural inflammatory response. I tried instigel and it really stung and made me worse. For me, that area of skin became highly sensitive and most products stung and made me worse, except natural oils and the saginil gel.

  • Posted

    Thank you Suki for this very long but very interesting recount of a problem that affects so many women. Well done for acting in a determined sensible way......your information will go a long way to help others.

  • Posted

    hey, i would be so interested to speak to you about where you went and who you were seen by in oxford.. i have suffered for over ten years now and seen many different "specialists" and tried many different drugs etc. nothing has worked and safe to say im desperate... im struggling to be happy and to know where to go for help next. 😦 thankyou in advance , melissa

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