Thread: Thoughts on SCS
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Old 08-28-2012, 12:32 PM
anon21816
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anon21816
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Smile Hi Moira

Glad you joined us on here its a great place for getting lots and lots of information and also for feeling 'at home'

I too have a SCS , since August 2010, and I wouldnt change it either. It does take a while to get used to it. Originally I thought I wasnt getting much benefit from it, but now 2 years on people have remarked how much better I look and I definitely feel so much better in myself. It does help me with Failed Back Syndrome and neuropathic pain in both legs.........Like Rrae said at times the stimulation does drive me a bit loopy but then I just turn it way down. Im still on reduced medication and Lidocaine patches and I find the combination of the lot help me a great deal.....

Im sure loads more will come on here and give you lots of useful advice. Do start a new thread also and then you will be able to just pop in and out of it at your leisure.....

Take care

Jackie
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"Thanks for this!" says:
eva5667faliure (09-05-2012), Mark56 (08-29-2012), Rrae (08-28-2012)