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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
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06-14-2012, 06:07 PM | #1 | ||
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Junior Member
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Hi guys, I had SCS surgery in December 11.my CRPS is in my left foot.I am still having severe pain around the surgery sites.Cant do much of anything.Still on crutches and in wheelchair.I would love to hear of fellow scs implant people.Im in UK and had my scs surgery at The Walton Centre .my neuro nurse check up is in August...any advice etc ?
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06-14-2012, 06:20 PM | #2 | |||
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lynn
You may want to post your thread on the scs/pain pump site. But in the meantime is there any ozzing or color change to the incisions? You may want to contact your dr. and tell them you are still in pain. You should not be having this much pain. 6 months out. Best of luck!
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. GOD help me be faithful in the midst of my suffering. Alt1268 |
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06-14-2012, 06:33 PM | #3 | ||
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Quote:
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06-14-2012, 06:41 PM | #4 | |||
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Co-Administrator
Community Support Team
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Here ya go Lyn,
SCS is a sub forum under Medications & Treatments SCS & Pain Pumps - http://neurotalk.psychcentral.com/forum118.html
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06-14-2012, 07:06 PM | #5 | ||
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Thanks. Im sure I will figure all the foruns out within the next 10 yrs..I need a HUGE arrow pointing to where I need to be. ,grins. Purrs n Smiles.
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