[magecharlie]

Looking for fellow pudendal nerve or SI joint dysfunction folks....

Anyone? For your sake I truly hope not.

MageCharlie

[Mark56]

However I am on the cusp of introducing a brand new line of items specifically worked out with those who suffer Tarlov Cyst in mind. A lead of one of the Tarlov Cyst foundations tried a prototype and her words were so very helpful, the most meaningful being "fantastic." For she has not been able to sit for many years without excrutiating pain. Since her issue is in the groin area, and I suspect yours well may be too, our Generation II, when it comes out, will not cure a thing, but it helps.

No this is not hype, just truth I share, you may ask Jenna, who has been here from time to time what she thinks, for she used it from Ireland to San Diego.

Nevertheless, I will pray for you dear Mage,
Mark56

[Packingheat]

Hi, I am a 41 year old male who has suffered for 2-1/2 years with pelvic floor dysfunction due to a work related injury that workmans comp is fighting. I recently went on short term disability and five weeks later my employer is terminating me. At least they agreed to continue my health insurance until my SCS trial and final implant if necessary. This is a CYA action due to my workmans comp lawsuit. I suffer lack of sensation in the last region any male would want and suffer another devastating disfunction that they don't make a pill for. The lack of endorphins and oxytocin in my system for this time period has me a basket case. The SCS will target the sacral nerves and pudendal nerve at a region in the middle of my back. I should have my trial within a month. I have at least been pain free due to a series of caudal epiderals over the course of about 14 months. I hope your dysfunction is not similar to mine. I will report back how the SCS works for me.

[Rrae]

Welcome Aboard!

I am so very sorry to hear of your circumstances.....and the work comp to boot. I know it can be a long drawn out process. I hope you have someone advocating on your behalf?
This forum is a great place to be for support and information. I hope you stick around and let us know when the trial implant will be.
There's plenty to read here and feel free to ask anything you'd like. We'll do our best to help any way we can.

Also, there is a forum here at Neurotalk specific to Work Comp. I know there is tons of info there. Here's the shortcut link to get you there:
http://neurotalk.psychcentral.com/fo...aysprune=&f=30

So glad you found us!

Caring,
Rae