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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Old 01-31-2012, 03:30 PM #1
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shello,

Welcome to the group is nice to have you. Sorry to hear you have this horrible disease. You will find this is a great place with kind people who are willing to give a lot helpful information. Feel free to ask questions, rant or rave or just participate.

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Originally Posted by shello View Post
Hi there,

I've had CRPS in the leg/foot since 2010, I have CRPS Type 2 from nerve damage. I've just joined to hopefully learn and share with others about CRPS and hopefully gain a better understanding of this syndrome. Look forward to talking and sharing.

Shello
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GOD help me be faithful in the midst of my suffering. Alt1268
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shello (02-01-2012)
Old 01-31-2012, 05:24 PM #2
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Welcome to Neurotalk! Sorry that you have CRPS...it is a nasty thing. I've had it since 2009, though I have type I. This is a great place to get support and advice and to just connect with others who have this condition. It has made such a huge difference in my life connecting with the people on here and finally feeling like I am not alone. As Alt said...feel free to ask questions or even just vent. This is a good place filled with very suportive and understanding people who can really relate to what you go through on a daily basis with this monster.
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Old 01-31-2012, 07:38 PM #3
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Shello, welcome to the forum! Sorry to meet you under these circumstances. Yes, a great place to learn, support others, and vent!

I have had CRPS in the foot since 2008, a complication of a (routine?) surgery.

No wonder you have to sign so much paperwork before you go under the knife!! HA.

Sense of humor is critical in dealing with this thing. Keep your chin up!
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Old 02-01-2012, 06:14 AM #4
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Just saying welcome and sorry you face this too. This is a very warm and educated community and I hope you benefit from it too.
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Old 02-03-2012, 01:07 PM #5
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Welcome tp the site. I joined recently and it's been a great help.Hope you make lots of friends and get the support you need. At least most of you guys are in a country that understands the disease. UK is a bit backward!
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