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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  • Edited

    How about Emuaid. And did you have any internal issues in the vagina?

    • Edited

      I'm not sure about Emuaid so sorry about that.

      The Vulva Clinic @ my local Hospital recommended that I only use Hydromol Ointment externally which I do; it's a good all round moisturiser and soap substitute (it can be purchased on Amazon in different tubes and sizes).

      I use Coconut oil internally (using a medical grade glove so I can avoid introducing any bacteria) and I know Suki will suggest YES Oil base lube.

  • Posted

    Hi Suki_girl

    If i were to write my experiences the story would be similar to yours in all ways except the initial cause was an infection which was secondary to irritation and inflamed vestibula (entrance to vagina). I'm still going through the process of repairing the damaged nerves , 6 months in, and want to thank you for your generous post about this topic. Thank You!

  • Edited

    Syren Intimate Relief Topical Treatment for Vulvodynia is a topical pain relief gel designed for the treatment of vulva pain and for conditions such as vulvodynia. Formulated with ingredients to soothe inflamed nerves, Intimate Relief is potent yet gentle when applied to sensitive areas.

  • Edited

    Hi I'm new here. I'm from Poland. I have vulvodynia since 9 years. I read your post Suki, which give me some hope. I have depression. I tried to take duloxetine, but I lost my appetite at all and I had insomnia. I try to take amitriptyline, but my body skin itches. I can't take any antidepressants because of skin itches. Maybe I should try the newer generation ones? I don't know what to do. I remember that I tried diet no dairy, wheat .. no results. I only stay home, I can't go anywhere. Here in Poland is so hard to find doctor who knows this disease. Everything is expensive - physiotherapy, visits, transport. I try to do my own physiotherapy at home, no results. I haven't noticed anything worsening my vulva symptoms. I just get these symptoms every day for no reason. It has started 9 years ago when I had infection of intimate parts. In 2015 the gynecologist said I have vulvodynia. He prescribed me amitriptyline. I took them half a year, no results. I try to take it now again, but what the hell is wrong with my body skin.. The neurologist doesn't know how to help me. Dermatologist too. I don't know how to cure my diseases.

    • Posted

      Itchy skin was one of the side effects I experienced when I tried to increase my dose, but that settled down after a month or two - it was horrible!

      I've been on Amitriptyline for nearly 15 months' and plan to taper off slowing over the next 3 months as I believe the symptoms I'm now experiencing are perimenopausal; we shall see as I reduce.

      Hydromal ointment has been massively helpful to me externally and coconut oil internally. I found applying an icepack (wrapped in a tea towel) to the area soothing and anxiety reducing; like a comfort blanket I guess lol.

      Stress exacerbated my Vulvodynia at the beginning so I try to relax and exercise each day so stay positive; things will and do get better.

      Read through Suki's original post and try everything detailed. I'm sure she'll respond once she's able to.

      Good luck!

    • Posted

      All these things I've read there are unavaiable in my country - from Hydromol, till Saginil gel. I can't take Amitriptyline. In this year I wasted so much money without any results. I want to try botox and thermolesion in the spine but I must wait for visit in pain clinic. I live in such a small city and it is impossible for me to go for Acupuncture or something like this. Probably next month I'll have biopsy, but it won't change anything, if I found out it's Eczema or something like this. I am devastated. I can't comprehend how an intimate infection can change your life forever.

    • Edited

      Could you try a pharmacy for an ointment solution similar to the ones that have been suggested here...?

      Perhaps look in your local supermarket for Organic Virgin Coconut Oil?

      Keeping a diary of what I have tried and the outcomes in relation to where I was in my monthly cycle was massively beneficial; I'm still updating the spreadsheet.

      Other 'Tricyclic antidepressants' are available for V so it is worth trying a different one to Amitriptyline?

      I believe my V is sensitive skin, stress and hormone related so what has worked for me might not for you, but... try everything like Suki said.

      Stay positive!

    • Edited

      I was at (new) dermatologist and he said my skin problem on my legs might be because of something pressures on a nerve (or several) in the spine or pelvis that's why he things I have itches on legs and all intimate areas. I also have problem with blood circulation in the legs, who knows maybe this problem I have also in in the pelvic areas, but I don't know where to go to check what is wrong with this. I had pelvic magnetic resonance imaging - good results. This pain kills me - all intimate areas, bladder, anus, low back pain. I take everyday rupafine, an antihistamine. At the moment I don't want to take any antidepressants, I must find out what is wrong that I have these symptoms. I use linseed oil and sometimes hyaluronic acid globules. I am not sure you heard about EMLA , it's strong lidocaine. It doesn't help me. I have symptoms from so many years, but this year is the worst ever. I'm sure I want try Botox, I can't wait what doctors will say there in Pain Clinic, but I am afraid I'll disappointed again. Thanks for your nice words, greetings ♥

  • Edited

    I just wanted to come on and give a positive update as it's so important people at the beginning of their journey no there is hope; it just takes time!

    I'm 90% back to normal after approx 15 months' of living with Vulvodynia.

    What has worked for me (if you haven't come across my other posts):

    • Hydromol ointment externally
    • Coconut oil internally
    • Acupuncture
    • Ice pack (wrapped in a tea towel) applied to the area
    • Comfy & loose clothing; ideally no underwear
    • Manual desensitisation
    • Amitriptyline (max dose for me has been 32.5mg)
    • Rest

    Have patience! It takes much time to get better and I found stress, anxiety and generally just being upset only made my V 10x worse! Setbacks did happen (UTI's etc.) but hang in there as it does and will get better!

    • Edited

      Hi WingGirl, thank you so much for your positive update. I think we need to see more such good news relating to vulvodynia on the Internet. There are so many doom and gloom stories that is can only put people in a negative frame of mind for recovery. I am so pleased my advice worked for you and you story, like mine, has shown that if you try multiple things, fund what works for you and stick at it despite the setbacks you can be pain free eventually. I have now been pain free for around 8 years.

    • Posted

      Thank you Suki_girl; you've been a massive help to all of us.

      I'm so happy you are still pain free!

      I'll keep in touch with my progress.

  • Edited

    Does anybody know why some women feel completely relief during period, and other have worst symptoms? What it depends on? From the work of hormones? Does blood supply and relaxation of the pelvis during menstruation affect? During period I have 99% relief. Exactly one day after this, I have bad symptoms like before period.

    • Posted

      This is sort of what happens to me.

      Most of the time I'm pain free during my period and then the pain returns for a few days' after as well as just before my period starts. That is what lead me to believe my hormones play a massive role and that perhaps I'm peri-menopausal as I experiencing other standard symptoms like hot flushing etc.

      Sadly since my positive post I've had a bit of a set back and the tapering of meds is on hold until the new year. I need to focus on getting completely pain free rather than being med free.

      I'm due for a blood test next week followed by a call with my GP to discuss results and the possibility of trying the tropical oestrogen cream. I also need to increase the pelvic floor exercises into my week as I've been a bit lax lately.

      Hopefully I'll have another positive update in a month or two.

    • Posted

      I'm only 30 years old. I can't have menopause yet. I don't have hot outbursts. Only my period lasts 2 days, but it is definitely due to stress. Have you checked your hormone levels? What blood test will you be doing? Basic? How often do you do pelvic floor exercises? Do you do them yourself or at a physical therapist? Of course I'll wait for your positive update. ♥ Take care ! I have visit at Pain Clinic next week. I don't believe that they will help me. My pain level is 10/10.

    • Edited

      I believe the blood test is to check hormone levels so my GP can ascertain my suitability for the tropical Oestrogen cream, but honestly, I'm not entirely sure lol.

      The pelvic floor exercises are from the book Suki mentioned in her original post; I do them at home a few times a week as well as some yoga moves.

      Good luck at your pain clinic appointment.

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