Dennis Taylor's Posts - Prostatitis Forum & Social Network2024-03-29T08:15:06ZDennis Taylorhttp://prostatitis.ning.com/profile/DennisTaylorhttp://storage.ning.com/topology/rest/1.0/file/get/303157292?profile=RESIZE_48X48&width=48&height=48&crop=1%3A1http://prostatitis.ning.com/profiles/blog/feed?user=06819vbcxjvpl&xn_auth=noBowel Movements and CPtag:prostatitis.ning.com,2011-11-08:2201951:BlogPost:278402011-11-08T19:21:38.000ZDennis Taylorhttp://prostatitis.ning.com/profile/DennisTaylor
<p>Has anyone with CP had painful bowel movements associated with it? Also, has it gone away after the surgery?</p>
<p>Has anyone with CP had painful bowel movements associated with it? Also, has it gone away after the surgery?</p>Chronic Prostatitistag:prostatitis.ning.com,2011-10-13:2201951:BlogPost:260322011-10-13T18:03:44.000ZDennis Taylorhttp://prostatitis.ning.com/profile/DennisTaylor
I just became a member on this site and have reviewed some of the information on the site. I had chronic prostatitis when I was in my late 30's and several anti-biotics were tried with zero effect. I had the problem for about 2-1/2 years when in about a 2 day period, it just cleared up by itself. Now almost 20 years later, I've gotten it again after a 3 month bout with epidydimitis. I was on Cipro for 30 days. So, for about 7 months in total I've had some kind of prostate pain with no other…
I just became a member on this site and have reviewed some of the information on the site. I had chronic prostatitis when I was in my late 30's and several anti-biotics were tried with zero effect. I had the problem for about 2-1/2 years when in about a 2 day period, it just cleared up by itself. Now almost 20 years later, I've gotten it again after a 3 month bout with epidydimitis. I was on Cipro for 30 days. So, for about 7 months in total I've had some kind of prostate pain with no other symptoms other than a bit of fatigue. I'm guessing ,from what I've read here, that there is no magic bullet and I just have to wait for it to get better just like last time. Does this pretty well sum up most people's problem? In other words, for those of us with CP, there is nothing out there.