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Old 10-08-2008, 08:37 PM #1
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Red face Hi, I'm new!!
Hi. Found this site looking up SCS. Wanted real opinions and not medical company propaganda!
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Old 10-09-2008, 06:01 AM #2
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Hi and welcome to NeuroTalk!! I'm not sure what SCS is (I tried to google it couldn't find anything) but hopefully someone will come along who is familiar with it and will be able to point you in the right direction.
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Old 10-09-2008, 10:22 AM #3
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Welcome to Neuro Talk glad you found us, like Kitty I am at a lost for what SCS means, i did go over my abbreviation sheet and did not find it. I am hoping someone else will have a link or knowledge of what SCS stands for, again welcome to NT glad you found us
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Old 10-09-2008, 06:26 PM #4
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Hi Gigi and welcome. Glad you found us. If you could let us know what SCS is we can direct you to the correct forum.

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Old 10-09-2008, 06:41 PM #5
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not sure what SCS stands for ... so i don't know what forum to direct you to ... still ... surf around and join in ... there are lots of friendly supportive and helpful people ...again ... welcome gigi to NT
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Old 10-09-2008, 09:14 PM #6
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Red face Sorry!!
Sorry about that, Spinal Cord Stimulator(SCS). If anyone has any personal info, I'd love to hear from you. I'm scheduled to have mine put in Nov. 11th and just wanted some honest opinions.
Thanks
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"Thanks for this!" says:
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Old 10-09-2008, 09:56 PM #7
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Hello gigi may i suggest posting a question in the spinal disorders and back pain forum, you will be likely to get a better answer then here in the welcome forum,, here is the link

http://neurotalk.psychcentral.com/forum22.html

dont hesitate to post questions.
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Old 10-10-2008, 12:11 AM #8
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Hello and welcome to NeuroTalk. Great to see you have come to be with us. Just let us know if we can be of any help.

Again welcome, looking forward to seeing you around.

Darlene
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Old 10-10-2008, 08:13 AM #9
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Hello and Welcome to Neurotalk!!

I myself don't have an SCS but many of my friends with RSD do. Everyone is different and some people swear by them and some people say that they don't work.

Here is the link to the RSD forum, many people there have SCS's so I am sure they will be more than happy to answer any questions that you may have. http://neurotalk.psychcentral.com/forum21.html

I wish you the very best of luck with the SCS and I really hope it helps you, please keep us all updated when you can!!

Alison
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