Hi, everyone.
 

My name is Denise and I was led to this community through an internet search. I have a 16 year old daughter who was diagnosed with RSD @ 3 years ago. (Her doctor now chooses to call this AMPS - Amplified Musculoskeletal Pain Syndrome). It's been a brutal 3 years for my daughter and those who love her, but I'm happy to report that, with treatment, she is currently sooo much better than before. We're hoping that she'll be released by the doctor this coming April. :) I'm here to gather as much information - and to offer as much support and hope - as possible.

Blessings to all!

WELCOME

may to follow with helpful
suggestions
hope she finds relief
in anyway possible
SORRY
no cure for RSD
this my DOCTOR instructs

MERRY CHRISTMAS

someone who cares

Nice to meet you!!
 

Denise,

:Wave-Hello: It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place.

That is such great news for her and her family. Give her a great big hug for us. If want to click in on the following forum, there are a group of friends to share with.

http://neurotalk.psychcentral.com/forum21.html

Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray:

:hug:

Hello Denise!
 

Welcome to NT! :hug:

You've found a wonderful place for support and understanding!
Make yourself right at home! Look through the forums and post anywhere you feel inclined. People here are easy to talk to in this down-to-earth atmosphere.

I hope you can find some answers for you daughter. It's great that you came here looking on her behalf. The RSD forum is absolutely full of great people and lots of support!

Just holler if you have any questions or need help in finding your way around. You'll find a friend around every corner!

It's great to have you!

Rae
:grouphug: