I am a 69 yr. old male. Had 2 TURP surgeries within last 2 years. 1st one was a total hack job and that's when my CPPS symptoms began. Had a 2nd TURP 9 months later that turned out very good as far as urgency and stream improvement but still pain that moved about in pelvic area from sacrum area, perennial area, penis, hips, bladder. 6 months after 2nd TURP had double Inguinal hernia repair. No improvement to CPPS symptoms though. Dr. put me on regemine of Oxycodone. Urologist recommended I read book: Headache in the pelvis by DR's Wise and Anderson of the Stanford Clinic. Book is a valuable source of information that describes "exactly" what CPPS is and symptoms. Signed up for 6 day CPPS seminar this month Aug. 2014. In the meantime, been going to a Physio Therapist in Bellingham WA. that specializes in Core/Pelvic therapy, MPT Elizabeth Hampton, EXCELLENT Therapist and highly recommend as she understands thoroughly about CPPS and addresses ways to help with myiofacial release and trigger point therapy. If you are a sufferer, I recommend HIGHLY you spend the money and time to at least read the book by Dr. Wise and Anderson and I completely understand how terrible having CPPS is and sympathize with all that have it. You're not alone. There are about 20k of us males that are diagnosed with Chronic non bacterial prostatitis that take antibiotics that DO NOT address the problem. PLEASE do yourself a favor and check this information out. I am posting as a victim of a botched surgery with 1st TURP that triggered this horrible condition and HOPE you get yourselves back on a program of recovery. God bless and good luck to all.
I too have the same kind of problem. I think I have IBS because I'm always constipated, and I have constant abdominal and back pain along with pain in the pelvic area. The doctor diagnosed me with CPPS but not sure on the IBS part. Did a bladder test and I was found to be completely emptying out my bladder after urination but it didnt feel like it. I think I have a kidney problem because I keep getting dull achy pains where the kidney is located on the left side of the back.
I know it's been a LONG time since you first posted this, but my situation is similar to yours....thinking you have something major but docs not finding anything. It is scary, but the longer I go I think it may be CPPS. I too have IBS and I don't think it's by chance that you and I are experiencing the same thing. If you get this and want to talk more, just respond to my post and we can talk further and see how much more common symptoms we have.
Good luck!
Anyone? I'm particualrly concerned about the varicoele in the right testicle which I believe is much rarer than the left hand side. Would this and possible thickening of the spermatic cord indicate a problem with the iguinal canal?