Hi,
So I have suffered a variety of different pain levels over the last 5 years a mix of vaginismus (inside pain) and provoked vulvodynia (outside pain).
I have gone through various different gp & gyno appointments and been signed off as having a perfectly healthy down below which still doesn’t explain my pain or lack of libido.
It was recommended I seeked a physco-sexual therapist, so I found one and am awaiting my appointment. However she did recommend that in the mean time I read a book called ‘when sex hurts – a woman’s guide to banishing sexual pain’ it’s an interesting read and backed with information from this book I convinced my gp to run hormone blood tests (for which I had to come off my contraception pill) and she has prescribed me amitrypteline at a 10mg dose to act as a muscle relaxant.
Since taking the amitrypteline I have managed to enjoy some ‘foreplay’ with my OH which will hopefully work to increase my libido again (fingers crossed) however I am still abstaining from my contraception in case they require more bloods so now the decision I have to make is to either find a non-hormonal contraception or start retaking my old contraception and hope they don’t require further bloods so I am able to test the work of the amitryteline at a 10mg dose before decided if I need to up to 20/25mg which is the max my dr recommended for me to try.
I will also add that I have and still try to persevere with vaginal trainers & a bio feedback Kegal Trainer but haven’t yet seen a noticeable difference. (Perhaps my next step will be to seek a trained physiotherapist after trying the therapist??)
Another book I tried reading was 7 steps to pain free sex, this has some pelvic floor exercises to try as well as intimacy exercises to try with your partner when you are ready to work on re-finding your libido.
I am still trying to learn more about this and other methods to try to solve the route of the pain in hopes to banish it…however it would appear that is can be linked to a lot of different underlying things such as Irritable Bowel Syndrome (which I suffer a bit with), Anxiety/depression, trauma or Auto-Immune diseases.
I have noticed that it is a very unknown thing and that’s because people just don’t talk about it openly…which I’d love to change….I’m just not sure how to go about breaking the taboo as I struggle to talk about it with my OH & drs let alone anyone else!