Accept it, Embrace it, Know that it is what it is, Buckle up, Hold on and join me on the "Journey of a Lifetime"! I am determined to win this battle with EDS and I want you to join me!
A JOURNEY WITH NO REAL DESTINATION
In December of 2010 I was diagnosed with Lupus/Mixed Connective Tissue Disorder. In March of 2011, I was diagnosed with Ehlers-Danlos Syndrome, type 3. The MCTD/Lupus Dx was incorrect, they should call EDS "ACTD", (All Connective Tissue Disorder)!
Since my Ehlers-Danlos diagnosis, I have read a few wonderful blogs that have inspired me and touched my heart. One blog brought me to my knees; I cried, my heart broke, I laughed, I smiled and I identified with this Katie's story. Reading her journey made me realize that I wanted to share my own.
Details are not something I spare and I have never been a girl of few words. I hope I inspire you, educate you, motivate you and touch your heart. I hope by writing this, I learn, understand and accept my new journey...Is there a destination?
Saturday, April 21, 2012
Comments
I think it is so cute that so many people read this, find me on Facebook and comment to me there. Just to let y'all know, it's okay to comment here too! Either way, I enjoy the feedback and questions!
Big Hugs!
Ila
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