Dr Peters talk about PN(E) besides other conditions. I found it very interesting.
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Here is the link:
http://www.blogtalkradio.com/pelvicmess ... -peters-md
I've had two pain doctors tell me to trial a SCS before I go through with TG decompression! They say it's too risky and the outcomes are too poor to be worth it. I understand their point of view. They are pain management doctors...they spend their life taking care of failed surgeries, but I'm only 30 surely I should try surgery before I go down the neuromodulation path. What if I was one of the 80%-100% cured ones? Then I'd be stuck with an implantable device that most likely did not take away my pain and could eventually stop working. Thanks for your input Amanda.Amanda wrote: The great thing about Neuromodulation is that it is "med free" and it is normally used from a physicians point of view as the last resort.
To use it before possible recovering surgery would be pointless; to try the surgery is the first option for any physician as neuromodulation is not designed to be a cure but a sympathetic response from the body to assist in the response from pain signals from the brain.
This is what I picked up on in the radioblog link Laura posted. Also he said in the blog that it was removable and that it could be replaced if it went wrong. And somewhere in there I'm sure he said that it made sense to go for minimally invasive surgery before major PNE decompression. But the blog is an hour long and I can't doublecheck that at the moment.Faith wrote:I've had two pain doctors tell me to trial a SCS before I go through with TG decompression!