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SCS & Pain Pumps For spinal cord stimulator (SCS) and pain pump discussions. |
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#1 | |||
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Junior Member
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Fine tuning is due Monday. Surprisingly, to me at least, as the incision site is healing, the program is changing. One of the two programs has somehow changed in frequency and pulse duration, even though that option is apparently not enabled on my stimulator. The manual states the option is available so I may ask that it actually be enabled. I think I like the idea of being llke to change the frequency and duration of the pulse. As an aside, I wear very strong hearing aids, which I asked my audiologist to let me program myself. Best aids I have ever had! From what I have seen so far, however, I am not ready to program the stimulator, although the prospect is intriguing. |
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#2 | |||
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Grand Magnate
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KOMA! Wow, I remember listening to that when I was a teenager - milleniums ago! At that time it was the ONLY good station we had available here in Toto-Land (Kansas). Boy, that brings back memories ![]() |
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#3 | ||
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New Member
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I am 56 years old, and have had "back trouble" since I was a child. I had scoliosis in my cervical and thoracic spine, and had a fusion when I was 11 years old. My doctors told me that I would be completely fine after I finished puberty. They said that once I finished growing, my bone wouldn't curve anymore. They were totally wrong, though knowledge of scoliosis has advanced at an unbelievable rate since 1966...My cervical and thoracic spine are wonderful today, but my lumbar is in rough shape. I now have a 70 degree curve! I fhave been on all kinds of pain med cocktails, but nothing works longer than a couple of days. I want to ask all you SCS people to tell me everything about it! What is the procedure like? How long does it take,and how painful is it? How long does the procedure take? Do you feel immediate relief What is the recovery like? What is it like wearing that belt and "recharging" yourself? It sounds a little weird to me...Please just tell mee verything you know about your experience, good or bad. I would just like t o be informed of what is coming my way. Thanks, everybody. Good luck to you, Silverfox! |
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#4 | |||
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Grand Magnate
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I'm sorry for these issues that are affecting your quality of life. Hopefully the SCS will offer you an effective form of pain control. Oh yes, there are many many questions that come to mind when presented with this thing. There's alot of info and testimonies here to read thru that you will benefit greatly from. Stick around! We're a great bunch and the support here is fantastic. It's great to have you! Rae ![]() |
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#5 | ||
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Junior Member (formerly Vivster)
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Glad you are healing well, and finding some programs that work for you!!
![]() Vivian |
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#6 | |||
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#7 | ||
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Junior Member
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Welcome Lizzylou~~I also was a stalker and just recently became a member of this site. I am 52 and have had alot of cervical and lumbar problems that ended with a 3 fusions. Anyway I found this site in hoping that I would get support and get my questions answered before seeing my neurosurgeon. I've been dealing with this pain for the last 10 years and I don't know how everyone else feels but I feel that my family and friends get tired of hearing about all of the aches and pains that I have---even tho they ask and seemed interested. You can ask all the questions here and everyone feels the same aches and pains as you do. That's one thing in common that we have--I don't know how great that is but at least we can vent our fustrations here!! Good luck to you
And now to end on hopefully a postiive note--I am scheduled for the SCS implant on January 3rd. Of course couldn't get it in before the end of the year for the insurance--hahaha I guess I shouldn't worry I will meet my deductible right away this year. IS that a GOOD thing or a BAD thing??? ![]() |
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#8 | |||
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Grand Magnate
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Well, I take the blame for that because I dragged my feet so long to get this thing ![]() Rae ![]() |
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"Thanks for this!" says: | Mark56 (12-22-2011) |
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