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Cata"MDJ gave me the chance to see that, in reality, I was not alone. It is my refuge. It means true understanding, shared knowledge, and support that is free of judgment. What I have received and given here is more powerful than I ever thought it could be. This place is all about love." (Cata)

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Chronic Fatigue Syndrome Support Group
A community of patients, family members and friends dedicated to dealing with Chronic Fatigue Syndrome, together.
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CFS & Others
Written by LJoDear   
04 April 2013

 

 Its nice to find a place like this. I was diagnosed with CFS about 3 years ago. It all started when I went to my doctor complaining of being tired all the time, not having any energy and out of breath. My family had gone on vacation to Panama city, FL and I had trouble walking on the beach. Muscles ached and couldn't hardly walk across the beach. Later that year visiting family I had problems going up and down the stairs, huffing and puffing. Now you have to realize I have always been very active, up at 6 am sometimes working on the job until 6 or 7 PM. Coming home to fix dinner, do housework, tend to the grandson, laundry, play and bed maybe at 11. Painting my house, yard work, running to stores, church... I am not one to sit still.

 



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Think You Have Only CFS? Think Again.
Written by jmudaisy   
06 April 2011

 

My doctor is amazing.  I went undiagnosed for more than 7 years, with doctors finally telling me I just had Chronic Fatigue Syndrome, and I'd have to live with it.  Finding a Lyme-literate doctor is like finding a diamond in the rough, and thank GOD that I did.  Check out his article:

http://www.iacfsme.org/LinkClick.aspx?fileticket=VcL5jCgZHa8%3D&tabid=458



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