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Spinal Cord stimulator battery pain

Chronic Pain | Last Active: 1 day ago | Replies (42)

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Profile picture for alexandercrps @alexandercrps

@cman55 Thanks again for the info. One important thing I have learned is that ice, even though it might feel as if it makes things better, it actually makes things worse. If she experiences burning in one or more of her extremities, this certainly suggests nerve damage. Furthermore nerve damage often leads to vasoconstriction, ie your nerves that normally control blood flow is now comprised. The limb basically gets chocked from its blood flow which makes the limb feel like it is burning but the affected limb is actually stone cold. Ice on
the limb may likely actually increase pain and make things worse; ice furter exasperates the said vaso constriction and I learned this the hard way. I used ice bags constantly in the beginning of my crps journey and it only made things worse. Ironically heat works better for nerve damaged limbs, at least this is my experience.
Lastly, I did understand that your wife had regular leads on her scs. I would still be sceptical to getting paddle leads especially given how poorly she is responding to the regular leads. It is also, as you know, a lot more invasive as they chip off a piece of bone to connect the leads…I understand that your docs want to try this route, I just worry about the torture and post op pain she’ll have to deal with and I just find it hard to believe that paddles is the fix to her issues. Have ya’ll discussed intrathecal pain pumps? If the scs fails she might be a good candidate for it. I’m sure you have looked into it..I havw both an Abbott SCS and a Medtronics pain pump so feel free to dm me or ask any questions you might have. I appreciate how stressful this situation is for you both and if there is anything I can do to
help then I am happy to.
Stay safe and I send you my best wishes

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Replies to "@cman55 Thanks again for the info. One important thing I have learned is that ice, even..."

@alexandercrps Thanks for your thoughts on this. Is using ice being counterproductive just for the condition you have? She hasn't been diagnosed with that condition. How were you diagnosed with that? What specialty did the diagnosis?
We have heard many times when trying to get a appointment "the Doctor doesn't treat that". They try to herd us to Pain Management. I want a Doctor the can diagnose her exact issue at the source. What I keep getting is no Doctor willing to except that challenge for whatever reason. To me that is just logic, they ignore that thinking.
We have a new Abbott Rep/Tech that so far wants her to contact her when she has an issue. The Rep/Tech is starting all over again from scratch attempting to get her better relief. I'm somewhat skeptical, but the rep seems sincere, so we are giving it another chance. She suggested new settings last night that allowed her to get some relief, and it helped relieve the pain. Extended relief would be nice, even 50%. We will see if we can get there. If it has been misuse of the SCS until now that would be the best case.
Maybe the first tech just wasn't the right one for her. We also have an appointment with the Surgeon that put her SCS in, as well as a Neurosurgeon at a different clinic to talk about her condition. No idea if we will be encouraged or discouraged talking with this new doctor. As for the laminectomy for paddles we really don't want to do that, or another surgery for an implant again if it can be avoided. As for the pump that would be a last resort that she doesn't want to do. We would need to learn much more detail about it.
Thanks for the info I'll certainly consider it, and it may be helpful for me to research, and ask the Doctors about it.