|
|
Reply
| |
hello,
My name is Terra,I am new to the site and am very interested in getting to know the other members on here. I have had RSD in my left leg for 3 years now, I feel it would be nice to talk to people who actually understand what I am going through and to be able to sympathize with them as well. I look forward very much to getting to know everyone on here. |
|
First
Previous
2-5 of 5
Next
Last
|
Reply
| |
hi there, I too have rsd in my legs only now, thanks to my great doctor who started ECT about a year ago. I actually had it in all four limbs, feet, ankles....... It was getting to the point that I could no longer manage a few stairs, or somedays not even leave bed. I got very depressed,, so the doctor decided to try Cymbalta. Oh what a mess that was. If you are bipolar, do not use Cymbalta. I was in the hospital 3 weeks. Not good. To see me now you could never tell I had RSD unless you spoke to me. I am able to ride my bike, lift weights, go fishing, things I thought were gone for sure. I still take meds, but not like I was, 31 pills a day. Good things do happen to people, yet some people won't take the step to get there. Best wishes, Sylvia |
|
Reply
| | From: lgs131 | Sent: 7/6/2008 2:20 PM |
Tomorrow my son will try transcanial direct current stimulation which is similar to ECT except they use a current 1000 times weaker than in ECT. He needs to have it done every day for a week and they say it takes 2-3 weeks to know whether it has made a difference. They are now doing a study on it at Beth Israel in NYC. If you have RSD in one limb, you can be part of the study. My son has it in 4 limbs and so does not qualify for the study but can have it as a clinical patient (we have to pay). I contacted WC to see whether they will pay but they will not pay for anything experimental so I have to see tomorrow just how new this is. I will update you on the outcome. ECT seems much more drastic and much more expensive so I hope this smaller current works. Sylvia, did your insurance pay for the ECT? Linda |
|
Reply
| |
Linda, Yes my insurance covers the ECT. Your son qualifies to have disability and Medicare. It's a Federal Law to deny SDI to anyone suffering from RSD. I have Medicare as my primary, then my husbands Blue Shield as my secondary. If you need any more info. in this direction, please let me know. I hope he does real well with his treatments. It is a true miracle the way it works. Sylvia |
|
First
Previous
2-5 of 5
Next
Last
|
|
|