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beth_ingram
01-25-2001, 05:16 PM
Has anyone had the staged trial for the Interstim? I had it done three days ago and am seeing some success. My problem was pelvic floor dysfunction and IC. Figure I'll have to wait another day or two to get rid of surgery aches to see if the PFD symptoms are gone -- don't notice any right now. Anybody else with these problems who had the Interstim? Thanks.

DebbieB
01-27-2001, 02:43 AM
Hi Beth:
I have PFD and I have IC as well ...
I did not have the staged trial, but I did have the trial before I got the InterStim Implant..
There is others on the board that did the staged, but I do not know if they had PFD,I hope some will post for you..
I had the InterStim Implant for almost two years now, been doing just wonderful with it and I am blessed each and everyday of life ..
I am different asI had my bladder muscle just die overnight and was unable to pee for two years and half,and had to self cath.
When I had the Implant turn on,a hour later I was able to pee on my own ..
It was just a wonderful experience too!!
I do not have anymore problem with PFD so far..
As I tell everyone on this board, we all so different in how we all handle the InterStim as well.
Good luck and keep us posted on how you are doing, we are all here for you Beth , if you have any more question ok.

Hugs Debbie

CaroleW
01-27-2001, 07:06 AM
Hi Beth, I had the staged implant on July 31 last year. I had it in for 5 weeks but saw no improvement. They tried every setting they could (the Medtronic rep) and still no luck. I am currently considering botox blocks of the pudendal nerve. Dr Richard Schmidt (who told me he invented the interstim) is the one who will do it. He is not on Blue Cross at present and we are waiting for him to get back on the list. Good luck, Carole Williams

tigger_gal
05-14-2005, 02:30 PM
I thoguht this was a WONDERFUL interstim success story to bring back to surface... I am sitting bored outta my mind and gonig thru old posts...
hugs
Brat

DebbieB
05-15-2005, 08:18 AM
Hi Brat;

I must clarify some thing that I typed on the message above ...
I DO have IC and was diagnosed in 1996 by having a cystoscopic with hydro and also a biopsy of my bladder..
I am sorry but I guess I should of poof read what I had type that day... :headbang: :headbang:


Debbie

tigger_gal
05-15-2005, 09:48 AM
thats ok .... We all make some major typo's here and there.. I knew you had IC... I didn't give it a second thoguht :) but glad you clarified it fo the others :)
Brat

emilyrose197377
06-05-2005, 11:52 AM
Does anyone know if interstim help urinary retention neurogenic bladder that causes ic?

thanks
Kim

patricia1
06-06-2005, 03:44 AM
Kim I have the Interstim. I do not know if it will help if you have retention...Interstim is for freq and urgency. It send pulse to the sacral nerves to help cut the feeling down of having to go to the bathroom all of the time. If you are having problems with not be able to feel the need to go to the bathroom I am not sure that this would work for you. As cuts down on the feeling of having to go all the time. Make sure you do your homework and talk to other patients that you dr has done this on....Maybe someone else will come along and know more...

emilyrose197377
06-06-2005, 03:45 AM
Thanks patricia

nsmith4366
03-16-2007, 12:45 PM
I had urinary retention and NOT IC - and I had PFD with spasms. I've had the interstim 1 year, no longer need to use catheter, no more PFD and the spasms are decreasing. My bladder still ACTS like it has IC (which is why I'm on the IC diet) but will take many years to heal (nerve damage) from growing to hold 26oz of urine before I got the interstim. The interstim only CURED MY PAIN BECAUSE I had pelvic pain due to urinary retention and spasms...not IC.