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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Old 07-14-2008, 11:58 AM #16
screwballpookie screwballpookie is offline
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Join Date: Jul 2007
Posts: 207
15 yr Member
screwballpookie screwballpookie is offline
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Join Date: Jul 2007
Posts: 207
15 yr Member
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Hey Desi,
Sorry it took so long for me to get back to you, I just all got busy again. I do have Rsd in my hands and arms,but I don't know for sure if it is in my feet. The reason i don't go to another doc is becuz When work comp and i settled out of court Dr. Panozzo is my authoriized doc and what he says goes. He is the only one that work comp will pay for and i can't afford to go to another one because i can't get health insurance. So I have to abide by this doc. He is a really good doc I just don't want to go in and hear that that is what I have. I guess I am just not ready to accept that there is a chance for it to be in my feet. Rsd has taken to much away from me now. The sad thing is now my attorney and I have to open to review because work comp is not holding up to there end of the deal so we have to go after them again. I have to pay for my meds out of pocket and turn the receipts into my attorney to get reimbursed which I am not cuz of work comp. By the time I pay for all my meds I need for a month it costs over $500 for ONE month. It just sucks.I just don't want to deal with hearing it from the doc again. It is very hard.I am trying really hard to keep my chin up but I have a lot of days that I just can't and I just don't know if I am ready to hear from my doc that the rsd has spread to my feet. That is why I am scared.

Sincerely,
Screwballpookie
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Desi (07-19-2008)
 


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