Does CP cause constipation?

Male pelvic pain, prostatitis, IC
ThisSucks!

Does CP cause constipation?

Post by ThisSucks! »

I know it can cause IBS, but often I feel constipated...Is this normal??

TS
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webslave
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Post by webslave »

Constipation is not related to CP/CPPS. Some people have IBS and diarrhoea (there does seem to be a relationship there, and one study supports it), some have constipation, but so do many normal people.

You may find one of your medications is causing it. Try a stool softener and more fluids.
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Post by ThisSucks! »

you don't waste any time do ya?? :lol:

thanks
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Post by alprost »

My physio mentioned that if you have pelvic floor muscle spasm, these muscles cannot relax as they normally would during the process of defecation, possibly resulting in constipation. I've noticed a big improvement in this area (particularly in the diamater of my stools, although that is probably more info than you need!) since undergoing myofascial release.
This is not Medical advice - Consult your Doctor!

Age:39. Age at onset:31. Symptoms prior to treatment: Golf ball in rectum, severe urinary frequency (2-3x/hr; 5-10x/night); weak stream; painful ejaculation; coccygeal pain; tip of penis pain; general pelvic pain on left; testicular pain; supra-pubic pain. Current | Symptoms: Urinary frequency 1x every 2-3 hrs and 1-2 x a night; mild pelvic pain on left hand side (all symptoms still improving!)
Helped by: Trigger point release; avoiding exercise; pelvic floor relaxation; Neurontin decreased bladder sensitivity somewhat. Worsened by: Exercise; frequent ejaculation; ibuprofen irritates bladder. Made no difference: Diet; biofeedback; quercetin; Steroid anti-inflammatories; Elavil.

****UPDATE*** I am now able to sit again at work all day, and can perform moderate aerobic exersise again for the first time in 8 years!!!

Please read:
viewtopic.php?f=37&t=808&p=3954
viewtopic.php?f=7&t=239&p=1158
viewtopic.php?f=37&t=248&p=1214
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Post by webslave »

alprost wrote:I've noticed a big improvement in this area (particularly in the diameter of my stools
Interesting data point :wink2:
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Post by Richard.N »

particularly in the diamater of my stools
I'm glad you've mentioned that Al. My stool diameter on Elavil has reduced considerably BTW.
Richard

Age: 39. | Onset Age: 30. Onset Date: January 2002. Symptoms (back then): Supra-pubic pain, back pain, urinary frequency, urgency and difficulty, weak stream, nocturia, (and variously) chronic fatigue, IBS. Current symptoms: more frequent than normal, but pretty much under control. Current amelioration: Xatral 10mg, Mirtazapine 30mg. | Worsened By: Stress, binge drinking, strained bowel movements, bloating, sitting on hard surfaces, jogging, and regularly - THE WINTER!

I'm not a medical expert. My comment is opinion. See your medical professional.
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Post by ThisSucks! »

alprost wrote:My physio mentioned that if you have pelvic floor muscle spasm, these muscles cannot relax as they normally would during the process of defecation, possibly resulting in constipation. I've noticed a big improvement in this area (particularly in the diamater of my stools, although that is probably more info than you need!) since undergoing myofascial release.
Hehe, thanks for the info...

Probly a stupid question, but what is myofascial release??
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Post by alprost »

ThisSucks! wrote: Probly a stupid question, but what is myofascial release??
'Myofascial' refers to the skeletal muscle and the connective tissue which surrounds it. The muscles of the pelvic floor are in a state of chronic spasm/tension in a significant number of chronic prostatitis / chronic pelvic pain syndrome patients, and myofascial release involves releasing this tension.

I think it works in the following way: The therapist applies pressure to a tight band of muscle which is in a state of spasm; this then causes a lot of pain in that muscle; in an attempt to 'get away' from the painful stimulus there is a reflex relaxation (release) in the muscle - I think it involves the golgi tendon organ reflex; however, when it relaxes and lengthens, the therapists finger 'follows' the muscle to its new position and applies more pressure; there is then another reflex relaxation of the muscle and therefore the muscle lengthens and returns towards it's normal length.

I'm no expert, and I would recommend purchasing the book 'A Headace in the pelvis' if you want to learn more about this: https://ucpps.men/the-wise-anderson-protocol

I had severe pelvic floor muscle spasm, and have improved around 80% by following a similar course of treatment to the one described in the book.
This is not Medical advice - Consult your Doctor!

Age:39. Age at onset:31. Symptoms prior to treatment: Golf ball in rectum, severe urinary frequency (2-3x/hr; 5-10x/night); weak stream; painful ejaculation; coccygeal pain; tip of penis pain; general pelvic pain on left; testicular pain; supra-pubic pain. Current | Symptoms: Urinary frequency 1x every 2-3 hrs and 1-2 x a night; mild pelvic pain on left hand side (all symptoms still improving!)
Helped by: Trigger point release; avoiding exercise; pelvic floor relaxation; Neurontin decreased bladder sensitivity somewhat. Worsened by: Exercise; frequent ejaculation; ibuprofen irritates bladder. Made no difference: Diet; biofeedback; quercetin; Steroid anti-inflammatories; Elavil.

****UPDATE*** I am now able to sit again at work all day, and can perform moderate aerobic exersise again for the first time in 8 years!!!

Please read:
viewtopic.php?f=37&t=808&p=3954
viewtopic.php?f=7&t=239&p=1158
viewtopic.php?f=37&t=248&p=1214