RSD in Me!







	Available on Amazon and Kindle All proceeds go to POPF

RSD in me!

RSD in Me! goes through aspects of Reflex Sympathetic Dystrophy Syndrome (RSD/CRPS) and chronic pain including definition, causes, tips on dealing with healthcare professionals, emotional aspects, caretaker information, of dealing with chronic pain and tips on coping with the pain.

Executive Director of the Power of Pain Foundation wrote this book as a pain patient, based on personal experiences in dealing with pain and the healthcare system. Barby earned a B.S.. in Social Psychology in 1994 from George Mason Univ. and worked as a Division IA Collegiate head coach and business owner until an auto accident in 2002.


The book is split into four major sections. How do you know What is next Working with healthcare professionals Tips and tricks for coping with RSD and other chronic pain issues Topics cover a wide range from history, causes, symptoms, diagnosing, psycho-social aspects, patients perspective, treatment plans, change in family dynamics, spirituality when in pain, working with the healthcare industry, helpful tips to use everyday and more. This book has been over 6 years in the making. It is written by a pain patient from her perspective we feel that it will touch the lives of many patients. Proceeds raised from the sale of this book go to the funding of patient grants and awareness projects for the foundation. Delivery of book can take 4-6 weeks. Books purchased directly from this site will come autographed by the author.

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Some of Barby’s thoughts on why to write a book on RSD.

A quote from the book
RSD In Me!

Not having enough information available, and having so many doctors try to treat me who did not know about RSD, I realized that I am the one who has to teach them. While teaching them, I have learned so much myself. Making this book and video series is the tool I wish I had found in my beginning stages. I want you to have the whole story. In my research I have found very little literature with the whole story; I know how important it is for the big picture. What information is out there? What is fact and what is fiction? What is old news and what are the newest options for patients?

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