I've had pretty substantial prostate inflammation and have never had any detectable PSA levels.
Substantial prostate inflammation and you NEVER had detectable PSA levels? Well then if mine is 0.5, I wonder what that means for someone my age. Guess I'll just have to ask and find out. Was your PSA level tested during an active bout of inflammation?
Well, I did kegels vefore bed last night, and not even overtrained, only like 20-30. Today, hard flaccid I guess could be called substantially bad, due to the fact that when I lay down, it IS giving me relief, but nowhere near as much as I usually get. It was actually still entirely hard for about a minute after laying down today, which NEVER happens. On top of this, on my way home from college, I felt this recurring pain in my perineum, really close to the anus or actually on the anus itself (whatever muscle/muscles that are associated with that are...)
I definetely know that pelvic floor therapy or trigger point message would not cure this condition, especially because I get that hourglass shape in my penis sometimes, which would be a structural problem with the penis. But maybe I could find some relief of the HF by getting pelvic trigger point message or something?
Hello guys I have some news.
Firstly i could not see my doctor right now so he referred me to another doctor. I met the doctor, very competent. She did not say i had nothing, she took it seriously. She said that i will probably need a surgery because there is something obstructing the blood to the penis. She thinks that i might have loosen something because of constipation. I told her i had hemoroids and other strange symptoms around this area and she said it was normal because everything is connected there.
So she put me to pass a abdominal ultrasound and will refer me to an urologist if i need to pass more test before the surgery (if surgery is needed).
I am going to keep you guys updated. Good day
So how many of you plan on going back to PE after we get better? (if the reason why your injury forum was caused by PE) Haha i think i'l be good once i'm all healed, at least for a while. I read that a few injured people actually do very light PE in order to re-stretch all the constriction/congestion and have seen more positive results to healing. I guess sort of like a physical therapy sort of thing...? Seems way too risky, not worth it to me. I suppose it doesn't help to be unaware of exactly what the problem is that's restricting blood flow and ultimately leading all of us to hard flaccid.
So how many of you plan on going back to PE after we get better? (if the reason why your injury forum was caused by PE) Haha i think i'l be good once i'm all healed, at least for a while. I read that a few injured people actually do very light PE in order to re-stretch all the constriction/congestion and have seen more positive results to healing. I guess sort of like a physical therapy sort of thing...? Seems way too risky, not worth it to me. I suppose it doesn't help to be unaware of exactly what the problem is that's restricting blood flow and ultimately leading all of us to hard flaccid.
I never did any kind of PE to begin with, but I'd be wary of doing it with hard flaccid at all. That tissue is meant to have some blood in it and be soft. Stretching it out when it doesn't just can't be a good thing. I had a uro appointment a few weeks ago and the guy grabbed my penis head and pulled it like a foot from my body while it was hard flaccid. It pretty much was in shooting pain after that for a good solid week straight. I think if anyone recovers from this they should thank their lucky stars and walk away from any questionable penis activity forever. Do you know how elated I would be to wake up tomorrow and see my normal penis again?! The thought of someone getting that feeling and then damaging it again with something they could totally avoid is pretty infuriating. To each their own though. It's your penis, or it was anyway.![]()
Hey guys,
Just got back from my appt. I had the exact same test Obitoo had with the exact same protocol. Done at the same lab with the same tech. lol.
So it showed with the waveform sensors that I had very little to no blood flow standing up whilst things were normal when lying down. When he did the ultrasound, my blood flow "spikes" (forgot the technical term) were a lot more pronounced when lying down and when standing, although present, were very very minimal. The color flow on the screen also looked a lot less prominent.
He reiterated the same thing obi did about the wand frequency needing to be higher to get a better picture of the arteries. He reccomended I find a place with a higher frequency to really get in there and get a better look.
I directed him to our website and also gave him a handout obi suggested to me regarding a non invasive test for measuring iliac artery blockages. He was not confident enough to perform that test at the time but he said he would check out the website and do some further research. Seemed like a really good guy.
I want to take these results to my next uro appt. and see if I can get more testing to get to the bottom of this blood flow issue. Will keep everyone updated.
does anyone else have testicle symptoms as well?? i can apply alot of pressure on my balls without feeling pain...I discovered this when doing a self examination in the shower...they are way less sensitive
when i stand up my penis changes its firmness and size, so does my brothers, so does my dad... so u guys are telling me we are all suffering from some disorder?
anxiety causes adrenaline.

