VVS and Mirena IUD
Oct. 1st, 2007 09:04 am![[identity profile]](https://www.dreamwidth.org/img/silk/identity/openid.png)
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Some back story....
A while ago I posted regarding pain during sex and since then I have been told that I have vulvar vestibulitis. As a treatment, I was given a topical cream to apply, however after about a month using that I discontinued use because I felt it wasn't working. At my next doctors appointment the nurse said that it looked like I had a mild case of BV so I had treatment for that as well...I don't go back to the doctor until november so I can't be sure that it's completely gone. This past saturday I started physical therapy for my pelvic floor muscles with a urogynecologist...I'm hoping that will provide some results. I was talking with the physical therapist regarding the supposed connection between HBC and various vagina-related issues such as vvs, vulvodynia and others and she enforced the fact that studies seem to allude to the connection, but never anything specifically conclusive.
I stopped taking HBC about a month ago to test for myself if my symptoms would change. I was on LoEstrin 24. So far, I haven't really had the opportunity to find out if there is any less pain during intercourse. I've been contemplating and IUD for a while and I'm leaning much more towards the Mirena than the Paraguard because I know I would not be happy with my decision if it resulted in heavier, more painful periods.
Anyway, I guess that the main question I wanted to ask was whether or not anyone here with vvs, vulvodynia, etc. has gotten the Mirena IUC after being diagnosed and whether or not it helped, hindered, or nothing changed with their symptoms. I'm wondering if the hormones in the Mirena are low enough to not cause a problem and I'm just trying to get a feeling of what I could potentially expect...or perhaps change my mind and go with a copper IUD.
Sorry for the long post, and thanks!
A while ago I posted regarding pain during sex and since then I have been told that I have vulvar vestibulitis. As a treatment, I was given a topical cream to apply, however after about a month using that I discontinued use because I felt it wasn't working. At my next doctors appointment the nurse said that it looked like I had a mild case of BV so I had treatment for that as well...I don't go back to the doctor until november so I can't be sure that it's completely gone. This past saturday I started physical therapy for my pelvic floor muscles with a urogynecologist...I'm hoping that will provide some results. I was talking with the physical therapist regarding the supposed connection between HBC and various vagina-related issues such as vvs, vulvodynia and others and she enforced the fact that studies seem to allude to the connection, but never anything specifically conclusive.
I stopped taking HBC about a month ago to test for myself if my symptoms would change. I was on LoEstrin 24. So far, I haven't really had the opportunity to find out if there is any less pain during intercourse. I've been contemplating and IUD for a while and I'm leaning much more towards the Mirena than the Paraguard because I know I would not be happy with my decision if it resulted in heavier, more painful periods.
Anyway, I guess that the main question I wanted to ask was whether or not anyone here with vvs, vulvodynia, etc. has gotten the Mirena IUC after being diagnosed and whether or not it helped, hindered, or nothing changed with their symptoms. I'm wondering if the hormones in the Mirena are low enough to not cause a problem and I'm just trying to get a feeling of what I could potentially expect...or perhaps change my mind and go with a copper IUD.
Sorry for the long post, and thanks!
no subject
Date: 2007-10-01 01:48 pm (UTC)But I do have a copper IUD. I thought the periods wouldn't be a big deal, because my periods were never all that heavy or crampy before. But for me, it did turn out to be a big deal. My periods are VERY heavy and VERY painful.
I chose the copper over Mirena because I was trying to see what impacts HBC was having on my depression. So in that sense, I still think it was a good choice for me. But I sort of blew off the seriousness of the heavier/painful period side effect...I wish I'd been more prepared for what that would mean for me.
Of course, YMMV. A lot of women don't have problems like I have.
Good luck with whatever you choose! :)
no subject
Date: 2007-10-01 05:20 pm (UTC)no subject
Date: 2007-10-01 07:31 pm (UTC)I noticed I felt tons better off birth control, but unfortunately, I was then diagnosed with endo and put on menstrual suppression for awhile. I can't wait to get off it. I used FAM for awhile, and I found my pain was next to nil during fertile days.. it seemed like everything just opened up and wanted sex! It was nothing less than amazing. It took about two cycles for my libido and lubrication to get back up and my pain to decrease.
I personally think that if hormones are the problem, it's either all or nothing. I felt the best I have in years using non-hormonal birth control. :)
no subject
Date: 2007-10-02 06:26 pm (UTC)I'm glad to hear that things are going better for you.
no subject
Date: 2007-10-02 04:40 pm (UTC)Also, I'd recommend checking out [Unknown site tag] if you haven't already.
no subject
Date: 2007-10-02 04:40 pm (UTC)no subject
Date: 2007-10-02 06:28 pm (UTC)I've been going to a Vulvar Clinic at a Women and Infants hospital near me and so far they've been really helpful. Much better than the gynos I went that told me that they could see nothing wrong so they didn't know how to explain my pain. I've also just started physical therapy, so I'm hoping that provides some results.
no subject
Date: 2007-10-02 06:34 pm (UTC)Capsaicin (http://en.wikipedia.org/wiki/Capsaicin) is the active ingredient in hot peppers. It's available by prescription; you can get creams OTC, but they're made for arthritis and usually contain vulvar irritants. MIne was compounded for me by a mail-order pharmacy after my doctor called in the script. It burns like hell (I sit on ice when I use it), but it helps tremendously, and after four years, I'm finally having pain-free sex again.
I hope PT helps; it's shown to be one of the most useful things for VVS. And I'm sorry you've had to deal with bad gynos.
no subject
Date: 2007-10-02 05:40 pm (UTC)