My blog has been moved to: http://cfs-facts.blogspot.com/
(http://cfs-facts.blogspot.com/) You’ll find the new research info there, as well as
personal observations about living with CFS/fibro. If you have a website or a blog,
please link to it!
One of today’s posts includes links to informational brochures and cards
that you can print up at home and hand out. A friend who has another invisible
illness always has a box of brochures in the back seat of her car, so when
someone criticizes her for parking in a crip space, she can educate them why
she’s there legally. So, that’s a good idea for the rest of us who sometimes
get flak for our disabilities.
We’re working on getting the www.CFSFacts.org (http://www.CFSFacts.org)
website back up and running, and will let you know when that’s done. Should be
in 6-8 weeks, but feel free to click at random intervals to see if we’re up
sooner than usual!
Karen
Founder, CFSFacts – dispelling the myths and providing the facts
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