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New Here too
Hi, I was diagnosed with Rsd/Crps in November 2011. I have had aggressive treatments and after several months of agony, I actually feel like my condition is improving some. I am looking for fellow sufferers who have lived with this condition for a long time and would like to get some tips on what has worked for them over the years, as from what I have researched it is probably going to be with me for the rest of my life as no known cure. Nice to meet all of you.
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Welcome to Neuro Talk!! :welcome_sign: Great to meet you and look forward to getting to know you! I have posted the link to the Reflex Sympathetic Dystrophy (RSD and CRPS) forum below...hope you are able to find answers to your question and also meet others who have the same diagnosis...:hug:
http://neurotalk.psychcentral.com/index.php http://i275.photobucket.com/albums/j...allwelcome.gif |
Hi there, just wanted to add my welcome!
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Greetings!!
cholmes67,
:Wave-Hello: Hello and welcome each of you to NeuroTalk. Happy to see you have come to be with us. Here are a great number of dear friends to listen when you are in need of ears. Please let us know how we can help you out. You will find out we are supportive and relaxing place. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you. :smileypray: Darlene :hug: |
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