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new member looking for Ballerina and fMichael
hi:
I do not officially have crsd, but I have body wide chronic pain. I am looking to talk to ballerina and/or fmicheal about tDCS etc. I am especially interested in a discussion on the devices. To start out, I did find this nice website: *** please excuse me being a bit blunt -- because one of the most nasty pain inducers for me is touch (mechanical allodynia), so I use voice dictation -- but and up using the keyboard a bit -- and I cannot use a keyboard very much before it is too painful..... |
Welcome to NeuroTalk.
You can find some information at RSD forum: This thread specifically: http://neurotalk.psychcentral.com/thread160980.html |
Hello & Welcome!!
Hello and welcome, happy to see you have come to be with us, it a great place to be. As you can see we have a great number and caring fellow members here, we are a supportive and relaxing place. Have fun looking into the different forums. Our shoulders are here for support in many ways. Check into the following forum: http://neurotalk.psychcentral.com/forum10.html Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. Darlene :hug: |
Darlene:
thanks! That forum will be very informative! |
Hi Voner!
....and Welcome to NT!
You should be able to find those members over on the RSD forum that MrsD gave you the link. Or, you can track them down by using the 'Members List' feature toward the top of the page.....the 3rd option from the left. (when you are at that page, the people search is clear over on the right side) Make yourself at home, there are so many caring and understanding people here! Caring, Rae :grouphug: |
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