My hopes are to bring more awareness to this intensely painful, crippling, and deforming disease. The reason I want to create more awareness is because currently there is not a cure for RSD and funding is desperately needed for further research.
My blog on how my life is seriously a circus! You name it I'll be writing about it. Make yourself at home and be sure to grab some circus peanuts, an ice cold beverage, and laugh with me as I poke fun of my crazy, silly life.
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Showing posts with label #RSD. Show all posts
Showing posts with label #RSD. Show all posts
Thursday, November 13, 2014
~ What Exactly Is RSD ~
In honor of RSD Awareness Month I am reposting the blog I wrote on RSD...please feel free to comment and share as we strive to raise awareness to find a cure for the most painful disease!
Since I'm asked quite often what RSD (Reflex Sympathetic Dystrophy) is, I decided to write a blog about the disease. The information in this blog post is based on the two plus years of research I have done on RSD. I will include a list of all the websites where I have obtained my facts at the end of this blog.
My hopes are to bring more awareness to this intensely painful, crippling, and deforming disease. The reason I want to create more awareness is because currently there is not a cure for RSD and funding is desperately needed for further research.
For those of you who do not know much about me, my name is Lysa and I was diagnosed with RSD almost three years ago. It took several months and specialists before they could determine what was wrong with me.
My hopes are to bring more awareness to this intensely painful, crippling, and deforming disease. The reason I want to create more awareness is because currently there is not a cure for RSD and funding is desperately needed for further research.
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