Wondering if you guys could help me out with my disorder, I have been trying to get my doctor to refer me to a urologist but she insists on doing and redoing blood work which has resulted in nothing but ia high liver enzyme.
I have had a aching feeling within my penis for the last 3 weeks now, it subsides sometimes and others its like a extreme ache followed by a shooting pain from the bottom to top of it, there is also a blueish tinge to a certain spot on the top part of the head near the foreskine and a darkening ring of the foreskin to a brown color. It doesnt hurt to urinate all that much, a constant flow, but seems a lot like I am never finished urinating, especially afterwards when I have small bits trickle out afterwards. I have been tested for all the stds and nothing. Could this be a form of CPPS? Any advice would be helpful, thanks in advance, R
pain
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MastCells
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Re: pain
Elevated liver enzymes can be a cause for concern, so it sounds like she's being a conscientious physician. What if any medications are you on, and do you consume much alcohol?RYAN wrote:Wondering if you guys could help me out with my disorder, I have been trying to get my doctor to refer me to a urologist but she insists on doing and redoing blood work which has resulted in nothing but ia high liver enzyme.
It certainly sounds like it could be a form of CPPS. I'm not sure about the skin discoloration.I have had a aching feeling within my penis for the last 3 weeks now, it subsides sometimes and others its like a extreme ache followed by a shooting pain from the bottom to top of it, there is also a blueish tinge to a certain spot on the top part of the head near the foreskine and a darkening ring of the foreskin to a brown color. It doesnt hurt to urinate all that much, a constant flow, but seems a lot like I am never finished urinating, especially afterwards when I have small bits trickle out afterwards. I have been tested for all the stds and nothing. Could this be a form of CPPS?
This is not medical advice. Please consult your physician.
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RYAN
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webslave
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Re: pain
This is not CPPS. chronic prostatitis / chronic pelvic pain syndrome requires at least 6 months of symptoms, and shooting pains are not a feature.RYAN wrote:I have had a aching feeling within my penis for the last 3 weeks now, it subsides sometimes and others its like a extreme ache followed by a shooting pain from the bottom to top of it
Good News! The great ProstaQ is BACK at last! You must try it.
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RYAN
ANY SUGGESTIONS OF WHAT I COULD BE FROM YOUR EXPERIENCE WITH THIS SITE? HAVE READ a lot OF POSTS HERE AND ON NUMEROUS OTHER FORUMS WITH NO CONCLUSIVE EVIDENCE TO SHOW IT IS ANYTHING, ANY TIPS WOULD BE APPRECIATED FOR THINGS I CAN BRING UP TO MY UROLOGIST WHEN I MEET WITH HIM, UNFORTUNATELY IN 2-3 MONTHS DUE TO OUR SUPERB HEALTH CARE
R
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MastCells
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Re: pain
You're right that it can't be classified as chronic prostatitis / chronic pelvic pain syndrome yet, but if he has these same symptoms 6 months from now, can you immediately rule out chronic pelvic pain syndrome as the diagnosis, just because he describes his chronic pelvic pain as "shooting?"webslave wrote:This is not CPPS. chronic prostatitis / chronic pelvic pain syndrome requires at least 6 months of symptoms, and shooting pains are not a feature.
Last edited by MastCells on Fri Jan 21, 2005 11:17 pm, edited 1 time in total.
This is not medical advice. Please consult your physician.
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RYAN
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webslave
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Shooting pains at the very beginning of chronic prostatitis / chronic pelvic pain syndrome are possible, in fact that's what I experienced once or twice during urination (right at the end of micturition). It is not a feature of long-standing CPP, in my reading.
This guy could have a number of things going on, and he's wasting his time here investigating this issue when he is only 3 weeks into symptoms with raised liver enzymes. Trigger point therapy is not appropriate for him at this stage.
This guy could have a number of things going on, and he's wasting his time here investigating this issue when he is only 3 weeks into symptoms with raised liver enzymes. Trigger point therapy is not appropriate for him at this stage.
Good News! The great ProstaQ is BACK at last! You must try it.
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LightningTree
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Shooting pains
Hi there,
Hope you are hanging in there.
During the first six months of my pain, I would sometimes getting shooting pains that, like an electric shock, would run up the left side of my penis. This happened most often when I was doing a particular stretch of my left leg.
This has not happened to me in six months, but my stretching is now more refined and does not include the offending manuever.
As my twin and I both have this condition,and I had shooting pains, I would say that shooting pains cannot rule out CPPS.
But in my humble opinion, I have to agree with others that at the three week mark you cannot rule out infection and should not label yourself with a chronic pain syndrome. Keep following your doctors advice and don't jump to undue conclusions.
Hope you are hanging in there.
During the first six months of my pain, I would sometimes getting shooting pains that, like an electric shock, would run up the left side of my penis. This happened most often when I was doing a particular stretch of my left leg.
This has not happened to me in six months, but my stretching is now more refined and does not include the offending manuever.
As my twin and I both have this condition,and I had shooting pains, I would say that shooting pains cannot rule out CPPS.
But in my humble opinion, I have to agree with others that at the three week mark you cannot rule out infection and should not label yourself with a chronic pain syndrome. Keep following your doctors advice and don't jump to undue conclusions.
This is not medical advice, and I am NOT a doctor of medicine or a related field.
* Age:33 Onset: February 2004.
* 99.9% IMPROVEMENT in 2.5 Years with the first year being the really hard part
* Current Symptoms: Mild irritation of perineal muscles on occasion. Relieved for days at a time by a specific stretch (see below).
* Initial Symptoms: Terrible penile, urethral, rectal, and perineal burning/aching with addition afferent sensations.
* Current Treatments: Deep stretching of the legs and pelvis. Most effective: Deep psoas and levitar ani stretch using the first phase of the "pigeon pose" from Yoga. When a deep pulling is felt in the middle of the pelvis next to the upper rectum, symptoms are completely alleviated for several days.
* Past Treatments Hyperprotection of the perineum for 1.7 years, Walking, Rectal biofeedback, Stanford/Wise-Anderson Protocol, Conditioned deep relaxation practice, Men's Multi-Vitamin and an Extra B-complex pill, all seemed to help.
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RYAN
thanks for the advice people, its very discouraging to try to figure this out as I'm sure all of you know from your own experiences, I will follow my doctor for the time being but knowledge is the key and research on your own must be done to rule out certain things, I just hope that this isn't a form of cancer!!! R
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LightningTree
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i empathise
Hey RYAN,
I understand how you feel. It can be very frustrating to have something so personal and at the 'center' of ones body, (at least I feel like it is) go so horribly wrong in a spirit-numbingly painful way, while doctors kind of mull around with vague diagnoses.
Personally, I've never had much luck with general practicioners, urologists, gastro-enterologists, and the like. I fell between the cracks of their respective fields and ended up being misdiagnosed, for the benefit of their psyches and work process, rather than for the benfit of my health.
Doing your own research is definitely the smart way to go. But keep an open mind to your doctor's advise.
And you never know, we all--doctors and suffers alike--have a lot to learn about the causes of these pain symptoms we share. Someday we may find definitive scientific evidence shedding light on a cause, and my guess is, it will leave everyone going "ooooohhh". No one will have precisely guessed/holistically absorbed the whole picture.
Since I and my twin brother both have CPPS, and got it within 2 years of each other, I tend to believe that its cause is unlikely to be from an invasive organism, but it still could be.
For my own two cents, if you still have symptoms after months of looking for pathogenic causes, try stretching an relaxing. It really helps me a great deal. I wish I could relax to the extent I do when I sleep, sleep makes my symptoms temporarily dissappear. How about you?
And just remember, if it is CPPS, it can get a lot better than it feels right now. I know my symptoms are far less now than they were last year.
hang in there, my pain got much less over time
I understand how you feel. It can be very frustrating to have something so personal and at the 'center' of ones body, (at least I feel like it is) go so horribly wrong in a spirit-numbingly painful way, while doctors kind of mull around with vague diagnoses.
Personally, I've never had much luck with general practicioners, urologists, gastro-enterologists, and the like. I fell between the cracks of their respective fields and ended up being misdiagnosed, for the benefit of their psyches and work process, rather than for the benfit of my health.
Doing your own research is definitely the smart way to go. But keep an open mind to your doctor's advise.
And you never know, we all--doctors and suffers alike--have a lot to learn about the causes of these pain symptoms we share. Someday we may find definitive scientific evidence shedding light on a cause, and my guess is, it will leave everyone going "ooooohhh". No one will have precisely guessed/holistically absorbed the whole picture.
Since I and my twin brother both have CPPS, and got it within 2 years of each other, I tend to believe that its cause is unlikely to be from an invasive organism, but it still could be.
For my own two cents, if you still have symptoms after months of looking for pathogenic causes, try stretching an relaxing. It really helps me a great deal. I wish I could relax to the extent I do when I sleep, sleep makes my symptoms temporarily dissappear. How about you?
And just remember, if it is CPPS, it can get a lot better than it feels right now. I know my symptoms are far less now than they were last year.
hang in there, my pain got much less over time
This is not medical advice, and I am NOT a doctor of medicine or a related field.
* Age:33 Onset: February 2004.
* 99.9% IMPROVEMENT in 2.5 Years with the first year being the really hard part
* Current Symptoms: Mild irritation of perineal muscles on occasion. Relieved for days at a time by a specific stretch (see below).
* Initial Symptoms: Terrible penile, urethral, rectal, and perineal burning/aching with addition afferent sensations.
* Current Treatments: Deep stretching of the legs and pelvis. Most effective: Deep psoas and levitar ani stretch using the first phase of the "pigeon pose" from Yoga. When a deep pulling is felt in the middle of the pelvis next to the upper rectum, symptoms are completely alleviated for several days.
* Past Treatments Hyperprotection of the perineum for 1.7 years, Walking, Rectal biofeedback, Stanford/Wise-Anderson Protocol, Conditioned deep relaxation practice, Men's Multi-Vitamin and an Extra B-complex pill, all seemed to help.
