This topic contains 3 replies, has 1 voice, and was last updated by  Roberto 3 years, 1 month ago.

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    “I would encourage you guys if your interested to google The wise-anderson protocol, Chronicprostatis.com(which unfortunately costs some money to join;however if this is your real issue its a goldmine of info), and research Chronic pelvic pain syndrome…I cant speak scientifically about the relationship between hpa dysfunction and CPPS, Im just a patient who is trying to recover a bit after having lived this nitemare for 5 years. It seems that its something that can be triggered by chronic stress, medications, infections, etc.. All I know is I share a lot of symptoms with finasteride sufferers although Ive never taken the stuff. Physical therapy is the main treatment; however its a disease that according to what Im reading needs to be attacked from many angles. Anyways, I dont want to derail the OP’s thread, but I hope Ive given you guys a good start on researching this if you think it might be your problem”.

    this mirror finasteride just like SE mirrors it .

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    yeah. CPPS can be mistaken for prostatitis.

    I’m thinking about trying to find some form of physical therapy to fight this. CPPS causes some form of hard flaccid.



    I’ve read some sufferers saying the Wise-Anderson protocoll is a scam.

    Have you managed to treat this horrible syndrome?



    I wonder if there is a connection between when you are sitting in front of the PC for 13 years in a garden type plastic chair?

    What I think is that my PC muscle can’t relax throughout the day.

    I started exercising,cycling.It’s good but it’s mostly sitting.

    Decided to walk up to the local mountain everyday and spend at least walking 2 hours in town here and there and see if it’s help my ED & soft glans syndrome,CPPS.

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