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Old 12-31-2011, 01:32 PM #1
Joydee Joydee is offline
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Join Date: May 2011
Posts: 92
10 yr Member
Joydee Joydee is offline
Junior Member
 
Join Date: May 2011
Posts: 92
10 yr Member
Smile New Member

Hi everyone,

I had signed up several months ago but only now introducing myself. In late
2008 my adult daughter developed CRPS after a survery to shorten the length of bone in the right arm and additional surgery on the riight hand.

Like many individuals on this site she has had several procedures done
without success. Over these months since I have been registered I
have been so moved by the suffering individuals have gone through as well
as the courage and hope displayed.

Recently I have become interested in TDCS. I am so grateful for the comments made by members fmichael and ballerina to name a few. It
was posts made by ballerina who is such an inspiration, had led me to
contact Atlanta pain center which is one of three centers providing TDCS
treatments. I intend to have a followup call after the holidays.

It is my understanding should sucess with treatments take place, for those
individuals like my daughter who lives hundreds of miles away, should
she have the capacity to do so, due to the ease home treatments, assistance could be given toward obtaining the device and instructions.

I would appreciate any iinput form other members reagarding the merits of
TDCS as well as home use.

Sincerely
Joydee
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Old 12-31-2011, 03:45 PM #2
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Rrae Rrae is offline
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Join Date: Nov 2009
Location: i thought it was in my left pocket
Posts: 4,117
10 yr Member
Rrae Rrae is offline
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Join Date: Nov 2009
Location: i thought it was in my left pocket
Posts: 4,117
10 yr Member
Laugh Hello Joydee!

It's wonderful that you are here at NT!

I'm sorry about your daughter's struggle with this nasty condition. You sound familiar with several of the folks at the RSD/CRPS forum, so this would be a great question to post over there.
You will be embraced with care and understanding. There's alot of good info as well. Check out the top section of that forum called the 'Sticky's'.

I wish you the best and hope for improvement in your daughter's quality of life as we enter into a brand New Year...

Caring,
Rae

...........................
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Old 12-31-2011, 08:29 PM #3
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Abbie Abbie is offline
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Join Date: Oct 2006
Location: In a DARK corner.... not looking for a way out.
Posts: 5,526
15 yr Member
Abbie Abbie is offline
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Join Date: Oct 2006
Location: In a DARK corner.... not looking for a way out.
Posts: 5,526
15 yr Member
Smile Hello and Welcome!

Hello JoyDee and WELCOME to NeuroTalk!

I see that you are finding your way around!

I too have RSD...8+yrs.

I believe there has to be something out there somewhere for us. Just remember that no two of us are affected the same by RSD and no two of us react the same to medications or treatments.

I hope your daughter finds relief soon.

Please feel free to roam around and join around anywhere!!

If you have any questions or need any assistance please don't hesitate to ask. Someone will always be around shortly to help in any way that we are able.

I look forward to seeing you around the board.

Abbie
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Old 01-02-2012, 01:45 AM #4
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Darlene Darlene is offline
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Location: Once a Texan, always a Texan.
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Darlene Darlene is offline
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Join Date: Sep 2006
Location: Once a Texan, always a Texan.
Posts: 11,976
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Wink Nice to meet you!!


Happy to see you have come to be with us, it a wonderful place to come, hello and Welcome. As you can see we have a great number and caring fellow members here, just let us know how we can assist, you will see we are a supportive and relaxing place. Have fun looking into the different forums. Our shoulders are here for support in many ways.

Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.

Darlene
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"Life without God is like an unsharpened pencil -- it has no point.
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