does anyone had an implanted pain pump?
does anyone had an implanted pain pump?
Do any of you know anyone who has an implanted pain pump for this condition and is it working out for them. I did a trial with bacolflin and it made the private area feel all engorged just like you were going to have a tooth pulled out.Not a good feeling I am looking for someone who has a pump that is using an opiate in the pump. Anyone beside Amanda with a successful stim for that matter.
Re: does anyone had an implanted pain pump?
The only person I ever remember posting good success with a pain pump was Barbi from the old forum. She loved it but I remember her doc had to place the catheter several times before getting it right. I don't know how many docs would have the patience to do that until they got it right.
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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Re: does anyone had an implanted pain pump?
I remember writing back and forth with "Peg" or "Peggy" from the other forum and she had a pain pump. I think it worked for a while but then her tolerance for the meds went up so high and her doctors didn't want to increase them anymore and she said it had become ineffective and maybe even had it removed This is to the best of my memory and it has been a while since we corresponded.
PN started 2004 from fall. Surgery with Filler Nov. 2006, Dr. Campbell April 2007. Pain decreased by 85% in 2008 (rectal and sitting pain resolved completely), pain returned in 12/13. Pain reduced significantly beginning around 11/23.
Re: does anyone had an implanted pain pump?
When i spoke to my two pain specialists one in Ireland and in belgium they regarded a pain pump as a last resort to pain management....the intolerance of pain medications and resulting dependance of medication makes this treatment the final resort. We did have a member who had many contraindiations in the form of absess's etc int he site of the pain pump. The whole idea is to reduce the medication useage and thats why Stimulation is a preferred option before a pain pump.
PNE started 2003 following Vaginal Hysterectomy, pelvic floor repair and right oophorectomy; eventually after many tests had BilateralTG surgery Nantes 2004; following this tried many other treatments including 7 day epidural, ketamin infusions to no avail; Trialed and was implanted with a Neurostimulator in 2007- Dr Van Buyten Belgium, this has enabled me to manage my pain much better.