 |
 | Home | Contact Us | FAQ | Search & Site Map | Link to Us |
 | Sign In | Join | Other 45 Sites in Network |
Medical Forum / Diseases and Disorders / Prostatitis / December 2005Best website for prostatitis
I read this group for a while, but I found a better place at http://www.chronicprostatitis.com/forum good luck all $20 to register?!?!?!?! what the hell kind of highway robbery is that? > $20 to register?!?!?!?! > > what the hell kind of highway robbery is that? My urologist cost me $4500 and didn't help me at all. Do the math. I think it's a bargain. Most urologists, and doctors in general, prime objective is to make money. They will often do what's easiest for them and whatever gets you out of their face the quickest, so they can see their next patient. Usually their lack of caring is obvious by their disinterested facial expressions, non responses to questions, etc. I spent over $6,000 on my prostatitis / cpps illness over the last 14 months for no reason. I'm finished with doctors. Lately I've started taking saw palmetto, cernilton and cranberry supplements, along with rooibos tea a couple times a day for the quercitin. I have less pain and more money in the bank. > Most urologists, and doctors in general, prime objective is to make > money. They will often do what's easiest for them and whatever gets you [quoted text clipped - 7 lines] > supplements, along with rooibos tea a couple times a day for the > quercitin. I have less pain and more money in the bank. ITA, my urologist seems to think treatment should start with a microwave procedure even though I got him to admit that my symptoms don't seem to indicate there would be much chance of it doing the trick. It was only because I had to take doxycycline as an anti malarial for a trip to the amazon that I found that gave me a lot of relief. He begrudgingly prescribed it for a couple of months at a higher dosage and I've been in pretty good shape for three months afterwards now. > Most urologists, and doctors in general, prime objective is to make > money. They will often do what's easiest for them and whatever gets > you out of their face the quickest, so they can see their next > patient. Usually their lack of caring is obvious by their > disinterested facial expressions, non responses to questions, etc. And don't you love it when they start blatantly yawning when they're talking to you, and I have even seen a few start closing their eyes when I was giving them my history, or some other info. I have spent over a million dollars going to over 75 doctors in my life and I have very little to show for it. It is very sad, and the medical world has become a joke in many aspects, and you can learn more by doing your own research...Pete I > spent over $6,000 on my prostatitis / cpps illness over the last 14 > months for no reason. I'm finished with doctors. > > Lately I've started taking saw palmetto, cernilton and cranberry > supplements, along with rooibos tea a couple times a day for the > quercitin. I have less pain and more money in the bank. > I read this group for a while, but I found a better place at > http://www.chronicprostatitis.com/forum > > good luck all Who are you trying to kid HubbaBubba. Changing your ID does not hide the fact that you show up here from time to time to promote your commercial website. Stay at your own forum and leave this one in peace. >> I read this group for a while, but I found a better place at >> http://www.chronicprostatitis.com/forum [quoted text clipped - 4 lines] > fact that you show up here from time to time to promote your commercial > website. Stay at your own forum and leave this one in peace. What the hell is wrong with that website? It is not a commercial website at all and the people who run it know a lot about the condition (more than most doctors). >>> I read this group for a while, but I found a better place at >>> http://www.chronicprostatitis.com/forum [quoted text clipped - 8 lines] > at all and the people who run it know a lot about the condition (more than > most doctors). NO RESPONSE, NC? Here's a link to some useful info I just found: http://www.cancer.prostate-help.org/capropsa.htm >>>> I read this group for a while, but I found a better place at >>>> http://www.chronicprostatitis.com/forum [quoted text clipped - 10 lines] > > NO RESPONSE, NC? Still no response from NC. Is he a coward? > >>>> I read this group for a while, but I found a better place at > >>>> http://www.chronicprostatitis.com/forum [quoted text clipped - 12 lines] > > Still no response from NC. Is he a coward? Usenet has lots of forums and you will get a lot of crap along with some good stuff. I prefer open forums where I can make my own judgement as to whether or not the post is worth reading. I don't need some self appointed censor making those decisions for me. That's the problem with prostatitis.com. If he doesn't lile you or disagrees with your post, it won't be seen by anyone. > Usenet has lots of forums and you will get a lot of crap along with > some good stuff. I prefer open forums where I can make my own > judgement as to whether or not the post is worth reading. I don't > need some self appointed censor making those decisions for me. That's > the problem with prostatitis.com. If he doesn't lile you or disagrees > with your post, it won't be seen by anyone. This forum is also censored. Not that it's worth it, with the few posts it gets. > "HubbaBubba" <HubbaBubba@iinet.net.au> wrote in message > I read this group for a while, but I found a better place at > http://www.chronicprostatitis.com/forum > good luck all Looking at the crap postings on this newsgroup, I cannot understand why anyone still posts here. Anyone who is serious about prostatitis and CPPS is over at http://www.chronicprostatitis.com/forum You know what I love. When I had CPPS 5 years ago and when the chronicprostatitis website was getting off the ground, it was formed in a response to moderated information coming from www.prostatitis.org. Ken tried to create these moderated groups that really allowed some dodgy characters to get their snake oil across. Like those two idiots in the philippines. The instigator of it all, the dreaded Anon, would jump on anyone who even suggested any type of commercial transaction. Now I see they asking for a $20 joining fee. So now they want money and they moderate the posts so only a specific viewpoint can get accross (sorry nature of moderation). How ironic is all that. By the way, Quercetin cured me. 4 years trouble free. > You know what I love. > [quoted text clipped - 13 lines] > > By the way, Quercetin cured me. 4 years trouble free. This newsgroup here is free, but just look at the value of the "information". Guys like Fatty Mawson who have been here for years, posting some new "cure" every few weeks, misleading poor guys just for fun, just for sh.ts and giggles. So if you want to pay peanuts, you get monkeys. If you think that http://www.chronicprostatitis.com/forum/ is not worth the small fee to join, a fee that is used to keep the site afloat, go back to your uro for more antibiotics. I hear $20 will get you a long way on that route ... might even pay for the fuel and parking for the trip. LOL! |
Reply to this Message |
 Sign In
 Join
 My Latest Posts My Monitored Threads My Blog My Photo Gallery My Profile My Homepage Start New Thread Enable EMail Alerts Rate this Thread
|
©2008 Advenet LLC Privacy Policy - Terms of Use
This website includes both content owned or controlled by Advenet as well as content owned or controlled by third parties.