St. Jude and question on Spinal Cord Stimulators (SCS)

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leftie1
New Member


Date Joined Jul 2010
Total Posts : 10
   Posted 7/15/2010 11:05 AM (GMT -7)   
Is anyone using the St. Jude SCS. This is what my dr. is wanting me to use. I go to the drs. on Mon. to discuss the SCS. St Jude will also be there. I want to get all the info before I go. What is the difference between the different kinds of SCS. Thanks, this is my 2nd time on this forum and it is great. Thanks to all of you for your input. Alot of people can benefit from ya'll. Thanks,

Leftie1

Post Edited By Moderator (Chutz) : 7/16/2010 12:21:21 AM (GMT-6)


Chutz
Veteran Member


Date Joined Jan 2005
Total Posts : 9090
   Posted 7/15/2010 11:20 PM (GMT -7)   
Hi Lefti!

I think I found the topic you were asking about in your other post. I added to your title so others with spinal cord stimulators will come by and offer you suggestions.

Good luck,
Chutz
If you're going through hell, keep going.

Winston Churchill

(\_/)
(o.o)
(> <) Co-Moderator Fibromyalgia & Chronic Pain Forums
Fibromyalgia, PTSD, UC, Diabetic on insulin, collapsed disk, arthritis scattered around and a few other delights.


Mrs. Dani
Veteran Member


Date Joined Jun 2009
Total Posts : 2787
   Posted 7/16/2010 8:02 AM (GMT -7)   
 
 
  Dear Left,
 
     Good morning! I hope you are having a nice morning so far. It sure is a georgous morning out here in New Mexico.
 
    I do not have a SCS myself, all I use is one of the little external devices but I think I can put together some links to help you with all your questions.
 
Forum Topics about SCS  ~~~>
 
 
Information about SCS ~~>
 
 
     I hope that helps a little. More so, I hope you can get enough relief to get some much needed rest.
 
*hugg*
  dani
 
TWO roads diverged in a yellow wood
And sorry I could not travel both
And be one traveler, long I stood
 
Chronic Pain Moderator

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