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Reflex Sympathetic Dystrophy (RSD) (CRPS) Message Board

Reflex Sympathetic Dystrophy (RSD) (CRPS) Board Index

Hi Drobin, and welcome. This is a great place to come for into, to talk, or to vent when you're having a bad day. Please share your story with us. How long have you had RSD? Where do you have it? Have you found a good PM? Do you have a stim or pain pump? Do tell! I have RSD in both of my upper extremities from a car accident on 12-29-02 (I wasn't at fault at all). So far I have refused the stim and pain pump (I feel it's too early in the progression of my condition, and I am also very fearful of anything that might stimulate my nerves as I've had bad experiences with that in the past). I take oral meds to help control it. I sing the praises of cymbalta for my depression and am in the process of weaning off of Neurontin and am starting to take Lyrica to see if it helps me more (I've been on neurontin for 3 years). I get frequent migraines and severe stress headaches and have had botox injections for them that helped me soooooooooooo much that I want to get the injections again. It's supposed to last for about 3 months but I had relief for 6 months which was GREAT because I found the injections to the back of my head and neck to be rather uncomfortable.

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