NeuroTalk Support Groups

NeuroTalk Support Groups (https://www.neurotalk.org/)
-   Reflex Sympathetic Dystrophy (RSD and CRPS) (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/)
-   -   Besides Pain Meds? (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/72572-besides-pain-meds.html)

Lonehunter21 01-20-2009 05:44 PM

Besides Pain Meds?
 
I recently had a follow up app. with my surgon, who operated on my left ankle on Oct of last year. I had ankle reconstruction surgery. I also suffer from RSD, which over the summer calmed down enough surgery became somewhat of an option. Being my only choice I said I wanted to go through with it. Now almost 3 months into it I'm still taking Oxycodon (sp?). I asked for a new script and he gave me this "speach" about still taking the pills and fear of addiction. But he gave me the ok to start PT and with the amount of pain I am still in I felt it was needed for me to get a new script, which I eventually did. He suggest that I get in contact with my neurologist to see if there is anything he can do for me or something else he can have me take instead of a pain killer. I'm sure there are other options out there, I'm just looking for some information to bring to the table for when I eventually seee my neurologist.

MominPainRSD 01-20-2009 06:37 PM

Quote:

Originally Posted by Lonehunter21 (Post 450274)
I recently had a follow up app. with my surgon, who operated on my left ankle on Oct of last year. I had ankle reconstruction surgery. I also suffer from RSD, which over the summer calmed down enough surgery became somewhat of an option. Being my only choice I said I wanted to go through with it. Now almost 3 months into it I'm still taking Oxycodon (sp?). I asked for a new script and he gave me this "speach" about still taking the pills and fear of addiction. But he gave me the ok to start PT and with the amount of pain I am still in I felt it was needed for me to get a new script, which I eventually did. He suggest that I get in contact with my neurologist to see if there is anything he can do for me or something else he can have me take instead of a pain killer. I'm sure there are other options out there, I'm just looking for some information to bring to the table for when I eventually seee my neurologist.

Hi there!! I would request that he refer you to a Pain Specialist.....preferably one that has dealt with cases of RSD before. They are more aware of the degree of pain that RSD causes and may be willing to work out a plan with you to continue your meds to allow you to do PT. Studies have shown that people in genuine pain do NOT tend to abuse their meds.....they simply want relief from the pain. Given that RSD is the most painful of ALL chronic pain conditions, that is a legitimate need.

The neurologist may prescribe you Neurontin or Lyrica.....both of which are good for neurological pain (the jabbing, stabbing, aching, tingling pain that tends to affect those with RSD). That would help you not need so much of your other pain meds, which would be a win win situation all the way around! Please keep in touch and tell us how your appointment goes!!

http://anesthesia.stanford.edu/pain/...%20Options.pdf

I cannot remember if I posted this link before, but it contains some good info. about general treatment of RSD.

Dubious 01-20-2009 10:45 PM

Thanks, "Mom," great article!


All times are GMT -5. The time now is 08:12 PM.

Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 DragonByte Technologies Ltd.