So I've posted on here a bunch of times about my completely lifeless penis (no feeling, no morning wood, basically zero sensitivity, just flops around lifeless and all) along with soreness and sometimes pain around my taint (perineum). I've been directed that it's more than likely CPPS from an overactive Pelvic floor. I was seeing a Physio for a while for internal massages and such and idk if that was really getting anywhere. The Physio referred me to see a urologist (have seen a handful in the past and they all said my penis looked okay which is complete BS because I literally cannot feel my penis and can barely get an erection) but this urologist that my physio recommended that I see was apparently familiar with CPPS/ Pelvic floor issues. I saw this urologist and he basically said Hard Flaccid is not a thing and he said to continue to see the physio and prescribed me some muscle relaxants to take before bed to calm down my overactive pelvic floor muscles. He also wants me to go see a Neurologist because he's sure it's not a blood flow issue.
My question is this, has anyone seen a Neurologist for this issue? If so what have they found/gained from it? Did it help?
I'm so fucking tired of not seeing a light at the end of the road. It's been over 6 years and things seem to have gotten worse. I'm willing to try anything... Anything. I'm lost. I'm desperate. Life is meaningless and depression is hitting hard as my mind tells me this is permanent and I'll never regain feeling in my penis. Help... Please...
My question is this, has anyone seen a Neurologist for this issue? If so what have they found/gained from it? Did it help?
I'm so fucking tired of not seeing a light at the end of the road. It's been over 6 years and things seem to have gotten worse. I'm willing to try anything... Anything. I'm lost. I'm desperate. Life is meaningless and depression is hitting hard as my mind tells me this is permanent and I'll never regain feeling in my penis. Help... Please...
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