My amazing Pudendal Neuralgia recovery with Michael Durtnall

Treatment options for UK & Irish members; including VHI & HSE criteria for funding and E112 Applications etc.

Re: My amazing Pudendal Neuralgia recovery with Michael Durt

Postby Marwa B » Fri May 19, 2017 9:36 pm

Hi Violet,

Thanks, hopefully we can return the conversation to a more constructive/progressive angle.

Best of luck to us all in this situation.

Marwa B
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Joined: Thu Apr 20, 2017 3:44 pm

Re: My amazing Pudendal Neuralgia recovery with Michael Durt

Postby Violet M » Sun May 21, 2017 4:37 am

Jason32 wrote:Wow... Uh, I am definitely NOT Ezer. I have the exact same screen name on TMS Wiki- you can read all my posts there, many of which even question mindbody. I have been told so many different things by different Doctors and PT's that I am naturally skeptical of everything. Apparently that's not allowed here.

That's fine, Jason. I never thought you were Ezer -- but for the sake of illustration it is fair to point out that your posts are similar to his. If you are going to be suspicious of other people, you need to understand that other people might be suspicious of you too. You and Alan want us to check out these other posters. How, exactly would you go about doing that -- other than checking IP's?

This forum has probably allowed more skepticism than many similar forums so your statement that we don't allow skepticism just doesn't fly. The reality is though, that if we allow skepticism, some people get mad. If we don't allow it, other people get mad. The moderators are all volunteers here trying to do our best. We are just asking that people be supportive and polite to each other. If that creeps you out, then this is probably the wrong place for you, Jason. I wish you all the best though and hope that the mindbody approach works for you.

PNE since 2002. Started from weightlifting. PNE surgery from Dr. Bautrant, Oct 2004. Pain now is usually a 0 and I can sit for hours on certain chairs. No longer take medication for PNE. Can work full time and do "The Firm" exercise program. 99% cured from PGAD. PNE surgery was right for me but it might not be for you. Do your research.
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Violet M
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