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Medications & Treatments For discussion about medications and treatments for any disease or health condition, including issues of medication toxicity. |
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Guest
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I was then sent to a Pain Management clinic and this Dr..(this is the guy who implanted my SCS) said that he wasnt a fan of Lyrica and over the next few months he 'weaned' me off them......I will say my head wasnt as woozie and I was started to make sense again, (well sense for me ![]() He then put me on lots of different meds over the coming months, ie Ketamin infusions, Lidocaine, Amitryptrelene, Zydol, Tramadol, Lidoderm patches, Rhizotomy...the list goes on....all still leaving me with the same pain, burning, tingling etc....so my last resort is SCS!!!! I do hope you get the relief you are looking for soon. Rae the fact that you are now using Lyrica etc, is that an indication that your SCS isnt working for you or isnt working enough? ![]() |
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"Thanks for this!" says: | Rrae (08-22-2010) |
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Grand Magnate
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I'm glad you asked this because i certainly don't want to mislead!! The SCS is doing WONDERS for me!! It has taken approximately 75% of the level 8 pain away! ![]() The reason I'm doing this Neurontin trial is to try to get away from the Lortab I take for the breakthru pain and the 25% that the SCS doesn't get to cover. I'm not taking Lyrica (like you, it was a very bad experience.....and this was 2 years ago......way before I had my SCS implant) I'm just simply wanting to see if Neurontin (which i hear so much about in helping with the burning neuropathy) will help bridge the window of my original pain and what the SCS doesn't cover... It's been 2 wks now on Neurontin and I actually think I'm seeing something change (for the better).....I'll give it more time to see for sure The SCS has been doing exactly what they said it would! I'm SO VERY grateful for this! I hope it lasts!! Thanks Jackie, you're great! Rae ![]() |
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