Chronic Pain members - Welcome, please introduce yourself

Hi,
I am a 48 year old lady who fell while ice skating in 2019.I basically put out my arm to stop fall and broke my wrist .I live in Ireland.I broke my wrist but had extreme pain straight away .I have been diagnosed with CRPS of my left arm and have had every treatment possible.Covid delayed a lot of my treatment.I had an Intellis SCS implanted 3 weeks ago.I had no trial .I am trying to find anyone with a similar SCS with arm CRPS .As I am trying to figure out this device Medtronic lady basically left it for me to setup.So just saw this forum and wondered if anyone had similar CRPS of arm and an Intellis SCS.

Hi, my name is Marina. Recently I was diagnosed with pudendal nerve neuralgia. I would like to connect with patients with this condition. thank you

Welcome @galwaygirl, There are a few discussions on the Medtronic spinal cord stimulators that might be helpful.

-- Has anyone tried the HF10 Spinal Cord Stimulation Device?:
https://connect.mayoclinic.org/discussion/hf-10-spinal-cord-stimulation-device-relieves-back-and-leg-pain/
-- Spinal cord stimulation: Will Nevro help when Medtronic didn't?:
https://connect.mayoclinic.org/discussion/nevro/
Sorry to hear the Medtronic rep left the device for you to setup. The manufacturer's website might have some helpful information on the setup and use.
-- https://www.medtronic.com/us-en/healthcare-professionals/products/neurological/spinal-cord-stimulation-systems/intellis-platform.html

Have you seen this YouTube video on the stimulator use and setup? https://youtu.be/Xr-lEtiRy4o

Welcome Marina @mgeasland, There is a discussion on pudendal nerve neuralgia where you can read through the posts and connect with other members with the condition.

-- Anyone out there diagnosed with Pudendal Neuralgia?:
https://connect.mayoclinic.org/discussion/anyone-out-there-diagnosed-with-pudendal-neuralgia/
Did your doctor suggest any treatment or options?

Oh my, that is not the "Medtronic Model" of patient care. You are going to need to be your own advocate to get the service and care you need.

It is the responsibility of their tech to help you get the machine set up and operating optimally. Please contact her, and work your way up through their customer service to get the help you need. They may need to assign a next-level technician if this is not the usual use of the device. If necessary, get your doctor involved.

Do you have contact information for the technician? If not, look into the material they gave you about the device to find it.
Sue

Were you able to have this corrected? If so, how?

Thanks for reply it good to have a forum to chat. I have no direct contact.I can leave message for her to contact me.But I did think it was not good enough .Will get my gp involved. It all so new for me.I found recovery harder than I thought it would be.They don’t really prepare for how long to recover.Wound site hurts when I drive with 3 young school age kids have to be able to pickups.But have to get husband to do for time being.

Thanks yes have searched the web thoroughly and found all that information.However my questions are really to do with Intensity and speed settings.Like it really hard to figure out where to start.Just thought if had someone else’s experience on Intellis with CRPS arm might get some help.

I have had several meetings w/ the thech and the doctor. The results have not been noteworthy.

Hi all... I have atypical trigeminal neuralgia and fibromyalgia, as well as depression and anxiety disorders. I've been on disability for many years. I'm in my 40's and I live on the west coast . I rode the opiate roller-coaster ride all the way thru rehab (a couple of times) and am currently begrudgingly and not effectively treating my pain with suboxone and deep breathing, the finest Western medicine has to offer.... Lol....may add some crystals and sage burning to round out my medical care... the system is so very broken