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Hello everybody, After having re-watched Dr. Antolack's videos about PNE (I had downloaded them wayback when they were available for download on Prostatitis.org), I re-concluded that this PNE thing exactly discribes my problem better than I could myself (symptoms etc). Now, I live in Montreal and would like to be evaluated and ultimately treated for this condition. How do I go about this? Is there anyone in Montreal or not too far from it that I could consult? Mr Ken Smith, any ideas? Thanks in advance

Hello everybody, After having re-watched Dr. Antolack's videos about PNE (I had downloaded them wayback when they were available for download on Prostatitis.org), I re-concluded that this PNE thing exactly discribes my problem better than I could myself (symptoms etc). Now, I live in Montreal and would like to be evaluated and ultimately treated for this condition. How do I go about this? Is there anyone in Montreal or not too far from it that I could consult? Mr Ken Smith, any ideas? Thanks in advance I spoke to Antolak late last year.  He's at the Mayo in Minn.  He's conducting a study, or was, anyway.  I'm sure he still is.  Minn. isn't THAT far from Montreal. Antolak sounded like a serious man.  We spoke for 10 minutes.  I declined his invite, and he told me I'd likely have this problem until the day I die. We had a good laugh.

Anthony & Sabrina < This e-mail address is being protected from spam bots, you need JavaScript enabled to view it wrote in message <news:%ovL7.5878$ This e-mail address is being protected from spam bots, you need JavaScript enabled to view it Hello everybody, After having re-watched Dr. Antolack's videos about PNE (I had downloaded them wayback when they were available for download on Prostatitis.org), I re-concluded that this PNE thing exactly discribes my problem better than I could myself (symptoms etc). Now, I live in Montreal and would like to be evaluated and ultimately treated for this condition. How do I go about this? Is there anyone in Montreal or not too far from it that I could consult? Mr Ken Smith, any ideas? Thanks in advance I spoke to Antolak late last year.  He's at the Mayo in Minn.  He's conducting a study, or was, anyway.  I'm sure he still is.  Minn. isn't THAT far from Montreal. Antolak sounded like a serious man.  We spoke for 10 minutes.  I declined his invite, and he told me I'd likely have this problem until the day I die. We had a good laugh. I hear there is a an enhanced MRI for pudendal nerve,it can be done only in California in Los Angelos.Apparently there are another 2 places in the world where it can be done,I just hope there is one in Europe. I have yet to hear that anyone has been benefited by the injection. There are 5 americans who had the surgery for entrapment. Basically everything started like this: In the 1980-s a British doctor became interested in pudendal nerve. French doctors followed it in France,and then in 1998 (I think) an american doctor went to france to have the surgery.Antolak went with him to have a look and then he started treating people in US for it. Another test for pudendal nerve it's called pudendal nerve distal modulatency.