Discussions that mention vicodin

Reflex Sympathetic Dystrophy (RSD) (CRPS) board


Hi Dietcoke:

I am from the DFW area also. I have had RSD for a little over 6 months now. Sure wish I could find a support group in our area. If you know of one let me know.

What treatments have you had so far? I have had 5 blocks and PT for 6 months now. I am on neurontin, zoloft, ambien and vicodin right now. I am scheduled for a consult for a SCS??? Not sure what I will do about this. I am still trying to get as much info on the SCS as I can and I am really afraid about having it???

Anyway.....hope you are having low pain days.

Nana
Quote from rsdnana:
Hi Dietcoke:

I am from the DFW area also. I have had RSD for a little over 6 months now. Sure wish I could find a support group in our area. If you know of one let me know.

What treatments have you had so far? I have had 5 blocks and PT for 6 months now. I am on neurontin, zoloft, ambien and vicodin right now. I am scheduled for a consult for a SCS??? Not sure what I will do about this. I am still trying to get as much info on the SCS as I can and I am really afraid about having it???

Anyway.....hope you are having low pain days.

Nana


There is a group in Plano that is strictly composed of people with RSD, and the info on them is below:

The RSD/CRPS Association of North Texas
For Sufferers of Reflex Sympathetic Dystrophy, A Chronic Pain Illness, their Families and Friends.

Meets every Friday from 10:00AM to 11:00AM at Columbia Hospital, Plano TX. For Further Information contact:
Jo Nell Fulwiler at 972-596-2955, Dr. David Hanks at 972-596-5960,
Lynda El-Mandouh at 972-406-1549
Becki Moore 972-644-5262


My treatment is too long to post and people probably would not believe it if I posted it. EXAMPLE: I've been to Mayo and Scott & White. I've seen 35 doctors (no joke). Literally, it would take me 2 hours to list the various "blocks" I have had, and if I did list them, you would all think I was an outright lunatic (and, perhaps you would be right).

Maybe I am insane. :(