My urologist subscribed an estrogen ring, for less pain for sexual relations with my man. I.m just assuming this is the reason, I'm not sure. It was alright for about 3 months. When I changed it for the next session, within 3 weeks I had to take it out it was so painful I couldn't stand it. I was wondering if anyone else has had any experience with this ring.
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I have used a ring since 03 and have had no problems.TREATMENT: PRN lidocaine/heparin Home Instillations since 2004
My Helpful Hints for Home Instillation: http://www.ic-network.com/forum/show...985#post309985
Institute of Female Pelvic Medicine (J. Dell, My MD) http://www.mypelvicmedicine.com/index.asp
Thank you for allowing me to share my experiences and offer support. Your physician is the only one to give you medical advice. I hope sharing the information from this site will help you and your physician develop successful management of your IC.
I post to encourage and offer total support for rescue instillations.
Find me on facebook: L. Clark Thomas
Louann
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I had a ring a few years ago and I thought it was irritating so I took it out. The last doc gave me cream, but I kept forgettin g to use it. So another doc has represcribed the ring because it is less of a dosage than the cream and more consistent. I haven't inserted it yet. Sort of nervous.I got IC in 1970! I was not diagnosed until 1991. I've tried many drugs and therapies but I tend to only resort to drugs when in a flare because when I am not in a flare (from being good on diet), I suffer only from small bladder volume (like about 7 ozs.) and peeing will relieve the discomfort. When I am feeling relatively normal, I say to myself I am glad I am not on a drug. When I am in a flare, I say, why am I not on a drug! I've recently have been trying to solve my connective issue problems in general. I look to diet and herbs mostly unless it gets really bad. I still think there is great hope for each individual finding a path to healing and there are many.
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