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

    Were u able to get off the amitriptyline? Im afraid ill come off it and itl come back?
    • Posted

      I too was afraid to come off it in case the pain came back. Long after I was pain free o started having discusssions with my GP about weening me off it but then I got hot flushes and night sweats due to menopause and amitriptyline helps with sleeping through the night sweats (many women turn to HRT because of lack of sleep) so my GP said because my body had adapted to the amitriptyline I may as well stay in it to help with sleeping during menopause. It seems to be working - I sleep well through the night. I only know I have night sweats because they wake my hubby up! So far I have not needed HRT. Just managing on the amitriptyline and using oestrogen cream for vaginal dryness. My GP did say there was no reason why I shouldn’t stay on amitriptyline for the rest of my life. Not sure I want to do that though ....
  • Posted

    Sorry I see u said u are still on it. Do u feel u areget pain free because of that or ur actually fully healed
    • Posted

      I think that I am pain free because I am fully healed. Amitriptyline alone never cured me, I needed the acupuncture for that. The amitriptyline helped me sleep and made me able to function better on a day to day basis. It was once I started the acupuncture that I really saw improvements after each session.
  • Posted

    Anyone else suffering from internal soreness too? 

    Swabs all came back negative.

    In agony today to the point I had to leave work sad sitting down is even agony! But yesterday no pain at all! 

    Still waiting on my womens health physio appt. 

    Hope everyone else is coping ok today xx

    • Posted

      I feel for you Hay, I really do. I was in such terrible burning pain at the beginning it felt like the whole area was on fire. Sitting was out of the question. Although I am better now the fear of that pain means that I rarely sit normally even now - I work mainly from home and sit on a donut shaped cushion (hole in the middle) designed for women who have just given birth. I also sit on one in the car. I am so afraid that it may come back, this condition that I never knew existed until 5 years ago.
    • Posted

      Its the worst 😢 lost so much confidence 

      I have ordered one of those pillows too, so hopefully that will offer some relief. 

      Dr put me in amitriptyline so keeping my fingers crossed 🤞🏼

      Also found this on  cvvd.org relating hypertonic pelvic floor muscles to vulvodynia. Hope the info is helpful to someone xxxx

      ‘This condition, also called levator ani syndrome or (and previously called vaginismus) is a common cause vestibulodynia (pain of the vestibule) and dyspareunia (painful sex). In this condition, the muscles that compose the floor of the pelvis and which come together in the back part of the vestibule (the pubococcygeus, puborectalis and transverse perineal muscles) become tight and tender. When these muscles are tight, less blood flows through them providing less oxygen to cells and resulting in a build up of lactic acid. The lactic acid causes the sensations of burning, rawness, throbbing, stabbing and aching so many women experience. In addition, it causes severe tenderness and redness of the vestibule near the perineum. . Women with pelvic floor dysfunction often also have urinary symptoms such as frequency, urgency and incomplete emptying of the bladder. In addition, constipation, hemorrhoids and rectal fissures (tears in the anal area) are common. Finally, women may also have low back and/or hip pain.’

    • Posted

      That is interesting Hay, and I think it applies to some of the women on here.  The website also looked interesting. I’m pleased to see that someone is working to help us!
    • Posted

      seems like thats the case for me although i have no redness and no issued with insertion or penetration. Does anyone have any sharp sensations when they walk ? Like little stabs. I dont really have burning anymore. 
    • Posted

      I get a whole range a pain from just a dull ache, pain, soreness, raw feeling, sometimes a stabbing sensation. 

    • Posted

      Hi Hay, how are you getting on with your pillow?  I too have a donut pillow and honestly I just can't cope without it.  It is invaluable, mine is disguised with a lovely tartan cover so it really looks like a normal pillow, which enables me to take it out everywhere, in the car, to restaurants, friends houses, etc.  I just tell people I have a bad back!!  It is so comfy to sit on, and I just can't cope without it, hope yours brings you the same relief.

    • Posted

      hi katie im just reading this thread ... I also have had penetration and it has been ok.. ! but its the general feeling of the skin inside the labia majora - prickly like and swaps from one side to the other. clothing seems to irritate mine and sitting for long periods or in certain positions ?! how are you going with it now ?

  • Posted

    Yes i used to also. amitryptaline stopped alot of it and pt . When is your pt session? You should be back to normal after a few months of pt smile
    • Posted

      How many mg of amitriptyline  were you on?

      Still waiting for my appt I cant wait to start!! I really hope this makes a difference. 

    • Posted

      It definately will. Im on 25mg of ami about three months now. That plus pt are a match made in heaven. Youll defo recover. How long have u had it and how old are u do u mind me asking. Also if u wanna pm me ur name I can add u on fb and we can pm message. Only if u want to x
    • Posted

      Hey Katie, im not on facebook unfortunately 🙁 im on instagram if you have that?

      Its good to know the amitriptyline is working for you, gives me hope! 

      I have been suffering i would say for about 6 years and im nearly 30. 

      My GP only prescibed me 10mg but i guess i need to go slowly and then increase and the side effects dont sound fun xxx

    • Posted

      Yes its important to start on 10mg I am 27 only have this since summer. But almost recovered. How have u jot had treatment for it untill now ? Yes im on insta. Pm me ur name x
    • Posted

      Glad your almost there 🙂

      I think i got told so many times its dermatitis so everything i tried made it worse and i kind of thought i just had to live with it. 

      This recent flare up though has been the breaking point where i thought i need to take this into my own hands. 

      I will pm you now x

    • Posted

      Hi katie!

      So glad to hear you are recovering

      Just like you, I just started off with 10mg of amitriptyline , how long before you went upto 25mg and when did you start to feel relief ?

      I started physcial thereapy as well,

      What did they do for you? And how many sessions did you go to?

      Glad this thread is growing!

      Good luck girls, we will beat this

    • Posted

      I was on 50mg a day. My dermatology consultant said I needed to be on 50-75mg. Because I git side effects I had to increase it slowly by 5mg every 2 weeks to allow my body to adapt.
    • Posted

      Started off on ten then a week later 15 then 20 week after then 25. Started to notice a decrease in pain within 2 weeks id say. In Physical therepy they manually release the tight muscles vaginally and rectally and externally and they massage sore spots to desensitize the nerves. They also address your diet. Let me know how you get on.
    • Posted

      How do you feel now Katie?

      After being on them for a week, I was starting to feel better and normal.. but now I feel the pain again and am still on 10mg... 

      Did you have ups and downs with the pain?

      I thought it would consistently be better once I started taking the amitriptyline everyday. 

    • Posted

      Your body will adapt to the amitriptyline. 10mg is not enough to deal with that level of pain. You need to be on 50-75mg.

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