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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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t.D.C.S. Update Could remission be within my reach and your's too?

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Old 08-01-2012, 11:02 AM #1
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Default HELP URGENTLY NEEDED - Ballerina's electrode placement protocols
Hi everybody,
Can anyone remind me what Ballerina's electrode placement protocols are?
I don't feel too good and it's a trawl through this mammoth thread.
She had luck with tinnitus, which is my area of need, using a pain protocol.
I would be terribly grateful for the help.
Also, anybody in touch with Ballerina, where's she posting now? If you speak
to her send her my best regards, thanks.

Wishing you all good health.

Nick
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Last edited by nick allen; 08-01-2012 at 03:00 PM.
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Old 08-02-2012, 01:04 AM #2
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Quote:
Originally Posted by nick allen View Post
Hi everybody,
Can anyone remind me what Ballerina's electrode placement protocols are?
I don't feel too good and it's a trawl through this mammoth thread.
She had luck with tinnitus, which is my area of need, using a pain protocol.
I would be terribly grateful for the help.
Also, anybody in touch with Ballerina, where's she posting now? If you speak
to her send her my best regards, thanks.

Wishing you all good health.

Nick
Hi,

I tried locating the info about tinnitus but the only post I saw off hand
ballerina mentioned, was page 1 of the TDCS thread, she said after one
week of treating twice a day the tinnintus had vanished. I do recall
another member had mentioned tinnitus as well but cannot recall who
that was. I could be wrong but perhaps CRP James. Have you tried
any of the protocols yet, if so which one.

I haven't heard from ballerina I hope she is alright.
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nick allen (08-03-2012)
Old 08-02-2012, 02:14 AM #3
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Quote:
Originally Posted by nick allen View Post
Hi everybody,
Can anyone remind me what Ballerina's electrode placement protocols are?
I don't feel too good and it's a trawl through this mammoth thread.
She had luck with tinnitus, which is my area of need, using a pain protocol.
I would be terribly grateful for the help.
Also, anybody in touch with Ballerina, where's she posting now? If you speak
to her send her my best regards, thanks.

Wishing you all good health.

Nick
Hi again Nick,

An additional response. You might go to Doc Fugedy's website
www.transcrainialbrainstimulation.com. Look under the condition
of tinnitus. He has some protocols listed there. Hope this helps
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Old 08-04-2012, 02:21 PM #4
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Default Sorry if I missed this
Didn't go thru entire thread so if info was posted, forgive me but my question is, I already own a TENS device (BNS 40) that my dentist prescribed for TMJ. Can this be used as A tDCS device simply by placing the electrodes on my head as opposed to my jaw?
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Old 08-04-2012, 04:30 PM #5
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Didn't go thru entire thread so if info was posted, forgive me but my question is, I already own a TENS device (BNS 40) that my dentist prescribed for TMJ. Can this be used as A tDCS device simply by placing the electrodes on my head as opposed to my jaw?
Hi,

That would be a no, but a tens unit can be used in conjunction with
a tdcs unit. Best wishes.
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Old 08-04-2012, 10:20 PM #6
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Default no luck
I am having absolutely no luck, No change in pain -NOTHING_ I am currently using a tens on my back as well as the tDCS

Deb
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Old 08-05-2012, 01:11 AM #7
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I haven't been allowed many treatment options so I haven't tried TDCS but I use my tens unit often.. though not directly on RSD area I do find that if I use it on surrounding area the spasms stop for brief periods. also I use it on my back and neck to treat for rediculopathy... it helps that with in turn is another minor relief. but like you all know minor relief is the difference of staying in bed forever or lightly living your life.
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Old 08-05-2012, 11:57 AM #8
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I am having absolutely no luck, No change in pain -NOTHING_ I am currently using a tens on my back as well as the tDCS

Deb
Hi.

Debbie I am so sorry to hear you are not finding relief with the new protocal
adding the tens unit with TDCS
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Old 08-08-2012, 04:45 PM #9
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Default Tdcs
I bought a phoresor II auto PM 800 from ebay and am having trouble with the electrodes. The machine came with built in alligator clip style electrodes that do not appear to be able to be changed. I tried clipping them to the amrex sponge electrodes but they wouldn't stay. I also tried clipping them directly plain sponges but that wouldn't work either. Does anyone have any suggestions for me? Sorry if I am missing something obvious.
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Old 08-08-2012, 07:54 PM #10
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I am having absolutely no luck, No change in pain -NOTHING_ I am currently using a tens on my back as well as the tDCS

Deb
I am very very sorry to hear this. I was hoping so badly that you would see some improvement by now. How many protocols have you tried? What has Dr. Fugedy said about your progress (or lack there of)? I really hope you find something that helps...
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