Thu May 10, 2018 9:43 am by Rosie21
Sat Aug 01, 2015 4:17 pm by Fielder
I'm a newbie. I live in the UK.
I'm trying to work out the best cushion to get for my vulvodynia. I suspect that I could have pudendal nerve involvement (the aching and burning pain is from vagina to clitoris) and I have rectocele and some tailbone pain too.
I have seen some good reports on older threads regarding the Putnams pressure relief cushions....with some ladies …
Fri Mar 08, 2019 10:57 pm by Persevere1990
I posted on here back in March 2017 having just got a diagnosis of vulvodynia after a few months of relentless and acute pain. I was desperate, I was hurting, I was scared I would never know life without pain there again.
I tried creams, acupuncture, numbing gels, frozen pads, baths with various internet recommended concoctions- convinced myself I had lichen sclerosus, herpes, thrush- …
Thu Feb 21, 2019 5:49 am by Jet227
Thu Feb 28, 2019 11:33 pm by PANDORA123
Fri Feb 08, 2019 7:35 pm by rl2091
I'm wondering if anyone has any experience with the MonaLisa Touch treatment for Vulvodynia? My pain started when I went on HRT(pill) for anxiety mainly and my pain abruntly stopped when I stopped HRT. However, when I started on the HRT patch (at my dr's suggestion), the pain returned and has never left. That was 7 years ago. I found MonaLisa Touch on the internet purely by accident …
Tue Jan 08, 2019 3:55 pm by flissyg
I’m so glad I’ve found a place where there are others who understand how I feel!
So this is my story:-
I’m 36, and 4 months ago, whilst innocently sitting in bed reading I experienced a very sharp stabbing pain in my clitoris. It last only a few minutes and then subsided as quickly as it came on. It put it down to “one of those things”. The following morning I woke up …
Wed Dec 05, 2018 3:26 pm by Cin124
About three months ago, I started having vaginal and vulval itching. Then, about two months ago, my vulva started to feel painful and look swollen, so I went to the doctor. I was tested for herpes, chlamydia, and gonorrhea which all came back negative. I also had to do a vaginal swab test and the only thing that came back positive was yeast infection. I was prescribed hydrozole …
Wed Jan 09, 2019 9:09 pm by Jma990o
So ok I'm 24 I've been having this problem for over two years seen quite a few doctors and obgyns alike and nobody will take me seriously I have had a few utis and yeast infections and even bv once and this all started after one of the utis …
I have FINALLY confirmed the date for my Vestibulectomy and it is happening next week at Chase Farm hospital in London. Although I'm super excited I'm also extremely anxious and nervous. I know that I will have a 'partial' vestibulectomy but my doctors have not told me how much that will be removed down there?? Reading through all the discussions here at this forum it seems like you all knew which parts that was removed (for example from point 2-10 or 4-8 and so on...). I have NO idea between which points they will remove my skin. When I had my second opinion my doctor draw on a piece of paper the area that would be removed and it looked like it could be from point 3 to 9 however I'm so worried as I feel my pain is from 2-10 at least....don't want the surgeon to take 'to little' and the pain will remain....
Now to the question: did you get the opportunity to meet/discuss with the surgeon on the day of the surgery? or did you just see a nurse and anesthesiologist?
I feel like I really need to know what will be removed prior to the surgery!!
Anyone who had vestibulectomy through NHS in England and can tell me how the procedure looks like? from the point of arrival to the hospital till the point when you leave?
Thank you so much <3
- Posts : 4
Join date : 2018-07-02