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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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Hi everybody! sorry I haven't been on in a long time...i have been in a bad place, really depressed and feeling hopeless. The pain clinic that I really don't want to go to is being pushed in my face. Worker's comp is making me feel like if I don't do it that I have no other options. Lots of you have gotten more stable without going to pain clinics...what do you all do?
I talked to a lawyer and they said to see what they had to say....then I could take that plan to a different place and get it done. They didn't give me a clear plan. i am confused and lost. My fiance JJ doesn't want me to go because I would have to leave home for around a month....coming home on the weekends only. They want me to go to a place to get off all narcotics and get on some med that starts with an S. I asked what I would do about flair-ups and they had no answers. Any advice? They also said that the narcotics are what made my rsd spread to all limbs.....anyone else heard of this. I know that there have been postings on it before but I missed those. Anyone have any research to back this? All the rsd sites I have seen don't say anything about this making it spread. sorry to come out and ask for help after I have been out for so long...but I need you guys. Thanks.... Lots of love and hoping that you all have been doing better! Jennelle |
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