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 12-19-2013, 12:57 PM #1
murgir murgir is offline
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murgir murgir is offline
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Default Great article very worth reading

http://www.rsds.org/4/stories/_keven_mosely.html
This article really made me feel better. I have not posted this but on Monday my doctor (Neurologist) said I was getting better and actually said I am releasing you. In my mind I though we all are better some days but brushed that thought away and thought ,,, He is a very smart man and knows more about conditions than I do. My hand would only sweat occasionally, color has been better, occasional pain, my swelling in some areas has not changed at all. My mental attitude changed after he said that. I did things around the house instead of sitting as much, I was on top of the world. Last night I burnt my finger and today my hand has sweated continually and seems more swollen. I am just sickened by this. After reading this article, I am not going to let this set back affect me as bad. I will try my best to just forget about it and keep going. He did say if something changes to let him know. I go back to work on 12/26 and will be using my hands a lot. I just hope I can do my work. I think going back will help keep my mind off me. Love you guys for all your help. I will not be able to be on here as much but WHEN I do get better..... I will continue to educate myself and share any positive findings with all of you. I loved that article it really lifted my spirits as much as so many of you have.
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"Thanks for this!" says:
Brambledog (12-19-2013), catra121 (12-19-2013), moosey2me (12-20-2013)
Old 12-19-2013, 01:41 PM #2
Brambledog Brambledog is offline
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I agree with so much of this! Thanks, I hadn't read his story...

When he said about doing 1.5 hours of exercise and massage etc a day, I smiled a wry smile...I may have mentioned a couple of times (lol ) that I have my hour a day most days that I do my CRPS management stuff - stretches, exercise, massage, and meditation. I have got back a lot of function with it, but not really lost the pain. I still get bad times, in fact I've been having a bad few weeks recently but I can still get about loads better than I did before.

I do believe in the positive attitude approach, and like most of us I try to be positive about it as much as I can. I think it does make a difference.

Good luck murgir Pop in to let us know how you're getting on every now and then, ok? I'll send some positive vibes your way I hope your return to work goes well, and have a wonderful Christmas and New Year!

Bram.
__________________
CRPS started in left knee after op in Aug. 2011
Spread to entire left leg and foot, left arm, right foot.

Coeliac since 2007.
Patella femoral arthritis both knees.

Keep smiling!
.
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Old 12-21-2013, 07:20 PM #3
Lottie Lottie is offline
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Thanks for the article - very encouraging and it reinforces a lot of the strategies all of us follow. I wish you all the best in your return to work. Have a pain-free New Year!
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1999 Chronic spine pain related to Degenerative Disc
Disease,
Sept 2001. C6 / C7 discectomy & fusion.
Jan. 2005 L5/S1 discectomy and Artificial Disc Replacement.
July 2011 removal of broken
.
Artificial Disc Replacement.
Woke up in recovery room with RSD Monster.:
.

Aug 2011 Stabilization of spine at L3/L4/L5.
October 2014 Rheumatoid Arthritis.
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