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Hello I am new to this blog but not new to urinary and fecal incontinence as well as cervical prolapse and general pelvic floor dysfunction. My 1st child was born in 2002 and second in 2004. I had small tears and a small episiotomy but other that that, they were normal vaginal births. As I expected I had stress urinary incontinence but didn't think anything of it.
I was a busy mom of two small children so I am not sure when all the other issues started. The first issue that bothered me enough to seek help was pelvic pain while menstruating. My gynecologist explained that I was suffering from cervical prolapse and in 2008 we scheduled a hysterectomy.
Since I was in my early 20's I have suffered from IBS due to stress and anxiety so I have always have had issues with diarrhea. The fact that I was leaking some when my bowels where loose didn't alarm me too much but I did seek help to decrease the diarrhea. The leakage turned into urgency fecal incontinence and I found a colorectal surgeon that through she could help. Come to find out, I had a 30% tear in my external sphincter. In 2013, my Interstim was implanted and gave me about a 50% relief at first.
In 2014, my fecal incontinence started getting worse, I thought it was due to the stress I was under going through a divorce. Then in 2015 a new symptom started, fecal incontinence during sex. If you thing that having a full bowel movement in public is horrendous, imagine dating for the 1st time after 20 years and becoming incontinent during intimacy. I immediately went to my gynecologist, (my colorectal surgeon was now out of network) who determined that my vaginal/rectal wall was extremely thin causing rectal prolapse. The feces would collect in the prolapse and was being pushed out during sex. I had vaginal reconstructive surgery to build up the wall. This surgery did not help at all. My boyfriend (now husband) was wonderful and we have found what works for us.
The incontinence has continued to get worse. I found a new colorectal surgeon, who suggested pelvic floor physical therapy. I have very little muscle function and am unable to Kegel. The exercises and biofeedback used in PT did not help. In 3 weeks I will be going back to my surgeon. The next step is another ultrasound and pudendal nerve test. Then my options are sphicteroplasty, stoma or continue to live in diapers and fear of people knowing that I have had an accident. Sphincteroplasty is basically out since I hear that the success is short lived and if I fail the pudendal nerve test, it will not help anyway.
I need input from others who know what I live with everyday. Your comments are requested.
I was a busy mom of two small children so I am not sure when all the other issues started. The first issue that bothered me enough to seek help was pelvic pain while menstruating. My gynecologist explained that I was suffering from cervical prolapse and in 2008 we scheduled a hysterectomy.
Since I was in my early 20's I have suffered from IBS due to stress and anxiety so I have always have had issues with diarrhea. The fact that I was leaking some when my bowels where loose didn't alarm me too much but I did seek help to decrease the diarrhea. The leakage turned into urgency fecal incontinence and I found a colorectal surgeon that through she could help. Come to find out, I had a 30% tear in my external sphincter. In 2013, my Interstim was implanted and gave me about a 50% relief at first.
In 2014, my fecal incontinence started getting worse, I thought it was due to the stress I was under going through a divorce. Then in 2015 a new symptom started, fecal incontinence during sex. If you thing that having a full bowel movement in public is horrendous, imagine dating for the 1st time after 20 years and becoming incontinent during intimacy. I immediately went to my gynecologist, (my colorectal surgeon was now out of network) who determined that my vaginal/rectal wall was extremely thin causing rectal prolapse. The feces would collect in the prolapse and was being pushed out during sex. I had vaginal reconstructive surgery to build up the wall. This surgery did not help at all. My boyfriend (now husband) was wonderful and we have found what works for us.
The incontinence has continued to get worse. I found a new colorectal surgeon, who suggested pelvic floor physical therapy. I have very little muscle function and am unable to Kegel. The exercises and biofeedback used in PT did not help. In 3 weeks I will be going back to my surgeon. The next step is another ultrasound and pudendal nerve test. Then my options are sphicteroplasty, stoma or continue to live in diapers and fear of people knowing that I have had an accident. Sphincteroplasty is basically out since I hear that the success is short lived and if I fail the pudendal nerve test, it will not help anyway.
I need input from others who know what I live with everyday. Your comments are requested.