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 05-09-2009, 08:40 PM #1
AintSoBad AintSoBad is offline
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Quote:
Originally Posted by CRPSbe View Post
Have you heard of this one, I found it to be a very helpful book!
http://www.amazon.com/Living-RSDS-Sy.../dp/1572243554

THANKS for that, Marleen!

Is it a good book to share with family?
(easy reading, or, will it just end up collecting dust?)
Just looking for your opinion...
Thanks again!


pete
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Old 05-10-2009, 09:33 AM #2
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Quote:
Originally Posted by AintSoBad View Post
THANKS for that, Marleen!

Is it a good book to share with family?
(easy reading, or, will it just end up collecting dust?)
Just looking for your opinion...
Thanks again!


pete
asb
You're welcome!

You definitely need to read it! Definitely! Whether it will be good for others who don't have RSD, I don't know. If they don't understand it now while you are explaining it in simple terms, then I doubt you can shove a book in front of them and make them read 238 pages.

I have it with me now and it's full of sticky notes and pencil marks from where I have read important, to remember bits. I have to say, it is the most comprehensive work that I have read about RSD. There are a number of personal stories in it as well. Sometimes it can get a tad "medical" but I don't find that at all disturbing. Chapter 7 for instance deals with RSD and "changing family dynamics" and I have marked this paragraph because it appealed to me and stated what I felt perfectly, "There are many books and articles that claim severe illness is a journey that can lead us to the true meaning of life. They say that illness is a gift we should be grateful for because, if we follow the writer's advice, we will be magically transformed into a new and beautiful spiritual whole. Let me just say that I feel many things about having RSDS, and none of them contains the word "gift." I would gladly have foregone the whole experience and lived a healthy, normal life. However, I do not have that choice."

Definitely a recommendation from me!

It's written by Linda Lang & Peter Moskovitz, MD and the money that is made from it is going to the RSDSA.

It is from 2003, and I don't think it has been updated with new research, so you have to keep that in mind.

I have a number of other recommendations besides that book, books on pain, if you're interested. None of that new-age crap about dealing with and overcoming pain, though (sorry if others believe in that stuff).
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All the best, Marleen
=====================
Work related (car) accident September 21, 1995, consequences:
- chondromalacia patellae both knees
- RSD both legs (late diagnosis, almost 3 years into RSD) & spread to arms/hands as of 2008
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Old 05-10-2009, 09:35 AM #3
Curious Curious is offline
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Karen if you need to add any questions, you can always make a poll here.

To be sure that only people with RSD answer, you can make it to show the names.
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Old 05-10-2009, 04:00 PM #4
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Thanks curious! Hadn't thought of that. :-) I know of one that I left out. I'll use the suggestion for the "missing" question, in a little while. LOL

Hugs,

Karen
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