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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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#1 | |||
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James, I have asked several times before not to be included on this list! I am having VERY successful results from both my cervical and thoracic stimulators. They had to change out the percutaneous leads for paddle leads in my thoracic SCS. This is not what I call a failure. To me, that "revision" was not a big deal, it was necessary and produces better results. I have NOT experienced spread because of them either.
I will not try tDCS, it's not for me. I cannot tolerate any of the medications or PT (or medication in the blocks any longer). SCS saved me! It gave me use of my hands and arm, so for now I continue to work because of SCS...that is success!! Nanc Last edited by Chemar; 05-03-2012 at 11:43 AM. Reason: quoted list was removed |
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#2 | |||
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Administrator
Community Support Team
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CRPSJames and/or ballerina (I am not sure who originated this list)
Please note that it is absolutely NOT OK to make lists and post them here about people's condition or their success or failure with any treatment That is a complete violation of their privacy! and, as one member has already mentioned, possibly erroneous info! If members want to post about their own treatment, that is fine, but you cannot make these lists and post them here
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~Chemar~ * . * . These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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#3 | ||
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Quote:
I can't speak to a list today since I did not see it or post it. In the past I posted in response to a question on how to locate posts about spinal cord stimulator revisions, spreads and or failures. I did a cursory search, only back several months and only mentioned those who posted their responses in those exact categories. I did not think that someone's post on a public forum about their response to a treatment was private information, only that which was sent in a private message. I only used the descriptions of the posters themselves with the reader being able to decide for themselves after reading someone's story that the risk of spread, etc. is worth it to them. I know many posters have listed my posted comments regarding my own reaction to treatments in addition to listing my name to look up exactly what I experienced, including treatments that have had side effects. I was not asked permission first. It would probably be helpful for all of us to know how to post and share this kind of information in a manner that encourages open discussion and self advocacy. Thanks Chemar! |
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#4 | |||
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Quote:
Nanc |
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#5 | |||
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Administrator
Community Support Team
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ballerina
the only time it is ok to quote another poster is on the actual thread where they have posted and using the quote button...it is not even ok to copy someone's post from one thread to another. Only members themselves have the authority to post about themselves...no one else is supposed to copy their posts or compile lists about them or anything else like that without their permission, and that permission would have to come from them to us, not just to you. Those lists you are posting are also somewhat in violation of our guidelines on using posts by members here to conduct "research"
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~Chemar~ * . * . These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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"Thanks for this!" says: | ballerina (05-03-2012) |
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#6 | ||
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But it is ok for someone to list me and suggest reading a particular post to learn more about my reaction to a particular treatment?????? I am unclear how using the search button to look up treatment outcomes constitutes "research." Do you mean it is OK to do that but it cannot be shared or posted? Thanks Chemar! |
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#7 | |||
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Senior Member
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I would like to know this too because I know I have suggested on a number of occassions that people check out the tDCS thread to read about ballerina's experience (and my own too but ballerina's story was particularly inspiring and is what led me to the treatment). If this is not okay I will not do it again. And if it's not okay with YOU ballerina I also will stop and I'm sorry if I ever overstepped. I always link to the thread though rather than relating the specifics of what you have posted. Just would like to check to make sure I am not doing something which violates anyone's privacy.
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#8 | |||
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Administrator
Community Support Team
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Quote:
I hope that clarifies and do remember, while these forums are publicly viewable, the site is privately owned with guidelines and Terms of Use which every member agrees to abide by when they register here.
__________________
~Chemar~ * . * . These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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