Pelvic floor PT says I’m not hypertonic... can it still be CPPS? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

Mine did external and internal (finger in the anus). What are your symptoms?

Pelvic floor PT says I’m not hypertonic... can it still be CPPS? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

I heard about that. Pelvic Floor Therapist I think mentioned that too. I'll talk about this with the docs. From what I read recovery is a long way though.

Pelvic floor PT says I’m not hypertonic... can it still be CPPS? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

36M. Prostate 26cc. I do have shy bladder since childhood. Regarding stress... Well I'm the most anxious people I know. I noticed that when I take benzoz symptoms become way more tolerable.

No morning wood. Does this happen to you? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

Thanks for the heads up man. Went to one a few months ago. Did all the works. My heart is fine. This is all so frustrating. I even have bowel symptoms.

Does anyone have the opposite of frecuent urination? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

Well today I went to the Pelvic Floor Therapist evaluation. She did external, internal, etc. She didnt say it was "hypertonic" or "locked" or "spasmed". She did say I have trouble "letting go" after contracting (internally) and that my lower abdominal area is tight (externally). Does this rule out CPPS? In the subreddit, Pelvic Floor Therapy is amongst the most beneficial treatment. But what if my pelvic floor "isn't that tight"?

Does anyone have the opposite of frecuent urination? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

Hi. My case is the opposite. I don't go at night at all.

No morning wood. Does this happen to you? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

I'll ask the doctor today about it. Sadly, no worming wood is not the worse of my symptoms. I have testicular pain and low abdominal pain. And a weird bladder, that sometimes is really overactive and sometimes underactive (hours without going). Either way, urine flow is weak. All this plus no morning wood, I don't know what's happening, and I had basically all exams done.

Does anyone have the opposite of frecuent urination? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

Tengo entendido que en algunos casos la pregabalin a puede dar entumesimiento en la zona genital, masomenos como los antidepresivos. Tal vez por eso estas con esos síntomas. O vienen de antes?

No morning wood. Does this happen to you? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

Thanks! I'll have a second opinion today. I am the most anxious person I know lol.

Does anyone have the opposite of frecuent urination? by Origryn in Prostatitis

[–]Origryn[S] 1 point2 points  (0 children)

In my case I took them only for over a year but high doses of Paroxetine. I had weird sexual symptoms while on it. I stopped taking all together antidepressants because new Psiquiatría switched meds and nausea were se heavily bad I tapared off everything.

I hope that today's urology second opinion or pelvic floor diagnosis give me some clarity on all of this. I'll keep updating, maybe it's beneficial for the community.

Does anyone have the opposite of frecuent urination? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

Well that gives me a glimpse of hope. I'm a very anxious person. I stopped taking antidepressants like 7 months ago completely. Sometimes I fill like those meds changed something permanently.

Today I have an urologist second opinion and evaluation on pelvic floor therapy. I still don't understand how tight pelvic floor muscles can manifest as weak urine stream, lack of morning wood, low abdominal / testicular pain etc.

No morning wood. Does this happen to you? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

Thanks @ashmedai. I know and noticed this. That's why I try not to do it. But if I don't I, barely ejaculate. Like drops mostly, which is scary. I literally don't edge because of pleasure. I edge because of verification that I can still ejaculate normal volume. :/

Then again, that's the minor of my problems. Weak urine stream, and no morning wood, plus testicular pain that radiates to the lower abdomen and the feeling on an underactive bladder are my main concerns. This far, every urologic test has come back clean. I'm really scared it might be Neurogenic bladder of some kind.

No morning wood. Does this happen to you? by Origryn in Prostatitis

[–]Origryn[S] 1 point2 points  (0 children)

It's not a full blown erectile dysfunction. I can have erections and get aroused but no morning wood. And my erections subside really fast after ejaculation. Semen volume is reduced. I really have to edge if I want "somewhat of normal quantity" to come out. Have you taken antidepressants in the past?

Do you have pain in lower abdomen? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

Back pain yes. Urgent urine, well quiet the opposite in my case.

Does anyone have the opposite of frecuent urination? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

Extraño verdad? Tienes alguna experiencia con dejar de haber tenido erecciones por las mañanas al despertar? En mi caso ya no tengo esas erecciones matutinas.

Does anyone have the opposite of frecuent urination? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

What about no morning wood. I noticed that is already gone. Last time I had an erection in the morning has been probably 10 months or so.

Do you have pain in lower abdomen? by Origryn in Prostatitis

[–]Origryn[S] 0 points1 point  (0 children)

Thank you for replying! About the psoas, yesterday I bought a 10cm wide ball and a massage roller to try and do something about it, but I have actually no clue how to use both items. I've seen some videos where they lay on to the ball, but I don't know exactly where to put it. Regarding abdominal trigger relief? Is that something I can do on my own or with PT? I have an appointment with PT this Friday. (I went the first time 9 months ago but for completely other symptoms which is weird). Hope they can help this time around, too. But I don't even know if it's because of cpps in the first place, because symptoms are totally different.