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Old 06-29-2011, 09:13 PM
Lorraine Shade Lorraine Shade is offline
New Member
 
Join Date: Jun 2011
Location: PA
Posts: 5
10 yr Member
Lorraine Shade Lorraine Shade is offline
New Member
 
Join Date: Jun 2011
Location: PA
Posts: 5
10 yr Member
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Quote:
Originally Posted by Paininthefoot11 View Post
I am new to this horrible syndrome.
My question is what physicial therapy are you doing for RDS/CPRS?
Are you going to PT? What is the therapist doing for you?
Are you doing things at home?

I just need some suggestions as what to expect/what to ask for.
Thanks for all your input.
I have RSD in both feet and now it spread to my hands and arms. I go to pain management and get injections. I also swim and lift weights. Pool therapy is the best. I go to DR. Schwartzman in Phila PA. he is well known nationally and internationally. Lidocaine infusions are supposed to be really helpful. The big problem is getting the insurance to pay for it, since it is considered in the experimental stage. Another DR. suggested Ketamine infusions, which I am seriously considering since I am out of work because I just had my leg reconstructed. My right leg is all metal from my knee up to my hip. I wake up in pain every day; but I try and keep a good attitude. I can't wait to go back to work, it takes my mind off of it. The big thing is to find a good DR. that knows about RSD and has some empathy, and really understands the disease.
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