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 10-11-2012, 09:49 AM #25
Hampster63 Hampster63 is offline
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Join Date: Apr 2012
Location: Long Island, NY
Posts: 32
10 yr Member
Hampster63 Hampster63 is offline
Junior Member
 
Join Date: Apr 2012
Location: Long Island, NY
Posts: 32
10 yr Member
Default All fellow tDCS users

So happy to see we haven't lost touch. It just seemed like no one was using tDCS so we had no info to respond to. I'm happy to see people are still using and hoping for some sort of improvement. I live alone and take care of my grandson only 2 days a week so if there were any noticeable changes I was not aware of there is no one to tell me there is a change. I still to this day do not notice any improvement. Last response with Dr Fugedy was 2 wks ago and he's waiting for something from WHEREVER? lol to this because I've heard 2 diff locations and both involve Europe. So take it with a grain of salt. Which is what I did. If I ever hear from him again I'll be surprised. Take a lesson.
When I use the unit I have 2 rubber head bands one for each pad specially when trying to do this by yourself with only 2 hands it is difficult. One band holds over the ear and one holds over the eye then I use a 3" ace bandage that I cut with velcro at one end. It works perfect to hold it all together once the pads are in place. So right now I'm not doing anything since no other protocol is available at this point. So you just hang in limbo. So to anyone else using tDCS please be happy with any help it may be to you. To those of us it has not helped we'll just keep praying for some other treatment to come along that we can put our hopes into. Hang in there everyone and always know we are all pulling for some each other. Much Luv to All.
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fmichael (10-13-2012), Joydee (10-13-2012)
 


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