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

    No Im in the United States and yes I am gonna start the search for good specialists. Gonna ask my doctor if she recommends anyone specifically as she seems to be educated or know about Vulvodynia. I will also mention increasing the medication dosage but I have only taken it a little over a week so i feel she would want me to try this dosage for a bit longer, I have a follow up in 3 weeks so I will mention it then. I have been kinda lucky in the fact that the symptoms have never gotten to the point where I cant sit, walk or wear clothing so i have still been doing all that however it is very mentally draining and as soon as i got home from work all i wanted to do was lay down and not move to no feel anything. I will keep yall updated on any progress or changes that happen. So glad i can talk to people that understand what im going through.

    • Posted

      I had something new come up today. After taking the amitriptyline for over a week the symptoms have decreased quite a bit , I would say discomfort level has been at a 1 or 2 instead of 5 or 6 like usual. After many months of not having intercourse i decided to do it today and I was able to enjoy it no pain , however after i noticed lots of swelling to mu left vulva area where i normally feel most of my discomfort and it is really red on that whole inner vulva area. I dont feel pain right now. Just wondering if anyone else has experienced this and if i should go see a doctor tomorrow ?

  • Posted

    Any problem is curable, we just need to take the right steps and follow the right guidance.

    • Posted

      Yes indeed. But finding the right guidance is a problem, especially with women's issues, it seems, e.g. vulvodynia, endometriosis, pelvic pain, vaginal atrophy. Getting a correct diagnosis for these things is a major undertaking in itself.

  • Posted

    hello! my Dr. say recently that i have vulvodinya.. so it was so depressive... sorry for my english ... please suky_girl let me know how can i send to

    you a private mesage ... i felt me so lonely i want to make to you some questions about it.

    thank you.

    • Posted

      I would really like to help but this site no longer allows private messaging and I tried to give you an alternative way in my previous message bit that got deleted by the moderator. You will have to ask your questions here I'm afraid.

  • Posted

    Hi i was diagnosed with vulvodynia two years ago ive tried pelvic floor therapy biofeedback compound numbing creams organic balms muscle relaxing suppositories currently on Lyrica ice packs while driving and sleeping cant hardly bare underwear im at my wits end my quality of life is so diminished i dont know what to try next

  • Posted

    i sm slso trying acupuncture

    • Posted

      You are doing the right thing by wearing no underpants. Have you tried sitting on a donut cushion (round with a hole in the middle). Keeping going with the acupuncture, keep going with pelvic floor exercises. You could try yoga positions to free up the pelvic nerves and manual desensitisation to retrain the nerves. Most importantly - are you on amitriptyline (or an equivalent drug)? Amitriptyline is a must.

    • Posted

      I am on Lyrica. I will try the yoga positions. And yes, I am currently using the bottom half of a cushioned toilet seat to sit on. Everything else I've tried seems to squish the area together making it worse. This seems to be a bit better. I've emailed the company in Italy re: the gel to see if I can get it shipped here. I'm awaiting their response. You are so helpful. Thank you from the bottom of my heart.

  • Posted

    Good evening,

    Is anyone still active in this discussion? I have some questions regarding hormones and amitriptyline (to name a few), and how they impact Vulvodynia.

    I'm still suffering and have been since the end of June.

    If anyone wants to reach out on here or by message I'd appreciate it very much!

    Thank you.

    • Posted

      Hi I'm still here! what were your questions? How much amitriptyline are you on now? What else have you tried - physio, manual desensitisation, acupuncture?

  • Posted

    Hello all!

    desperately battling a vaginal condition, its been three weeks. it started off as a sensation like i am being poked by little needles. progressed to bad itching. gp put me on thrush medication, nothing helped. all swabs came back negative. referred me to a gynaec, but appointment is in jan 2022 and it november 21 yet.

    i was getting so much better but 3 days back it came back. its again needle sting sensation. i was trying to do my research when i stumbled upon this thread.

    i had something similar back in 2016 when i was pregnant with my second child. at that time it all continued for 5 weeks and disappeared miraculously once in gave birth.

    never thought it could be vulvodynia. i am using coconut oil atm. today got dermol 500, will try that as well.

    my questions are:

    1. shall i ring my gp and discuss this vulvodynia thing with her? i have been seen by gp to check for any dermalogical changes down there but nothing.
    2. shall i wait for gynaec appointment which seems far away, or shall i go and see a private gynaec?
    3. can i start researching about accupuncture and physiotherapy stuff?

    i am very scared after reading all of the things here.

    • Posted

      if there is no infection and no dermatological changes it sounds very much like vulvodynia. The sooner you start working to cure it the better. You could see a private gynae to get a formal diagnosis - you need to find one who specialises in vulva conditions or you can start doing all the things that people have found to work on here. You will need to be prescribed amitriptyline and that could be from a gynae or your GP. I was lucky to have a GP who had seen many patients with vulvodynia before but she wanted a diagnosis from a gynae first.

    • Posted

      thats what i was thinking. i should start working on it asap. i have a gp appointment in two days but i have a hunch she is not going to prescribe me something like amitriptyline without a gynaec consult. i am trying to find a private gynaec who specialises in vulval diseases. i am trying to

      find a western accupuncturist near me as well. i just hope i find light at the end of the tunnel

      a bit sooner. thank you for taking time out to

      reply.

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