Fibromyalgia & Chronic Fatigue Syndrome Awareness Day
May 12, 2010
Objective:
To help create more awareness and better understanding of Fibromyalgia & Chronic Fatigue Syndrome (CFS/CFIDS)
The day is dedicated to educate people about Fibromyalgia and Chronic Fatigue Syndrome. This day is to help people establish a better understanding of these illnesses.
To learn more about Fibromyalgia Awareness Day, please visit the National Fibromyalgia Association website at:
www.fmaware.org/site/PageServer?pagename=community_awarenessDay20...
While you are there, please take a look around. NFA provides a wealth of information.
To learn more about Chronic Fatigue Syndrome (CFS), which is also known as Chronic Fatigue and Immune Dysfunction Syndrome (CFIDS), please visit the CFIDS Association of America website at:
www.cfids.org/default.asp
5/12/10 Please Submit!
Today is Fibromyalgia & Chronic Fatigue Syndrome Awareness Day!
Please remember to submit your articles at Bloggers Unite, so that everyone can read your post :)
Thank you!
Nancy
Chronic Connection
5/09/10 Welcome & Thank You
Just wanted to take a moment to welcome all the recent participants that joined this event! Thank you for uniting with us!
-
ChronicConnection
event organizersee more 24 BLOGGERS PARTICIPATING
-
Fibromyalgia & CFS Awareness Day ~ May…
http://gentlehugs.livejournal.com/38247.…
Fibromyalgia & CFS Awareness Day ~ May 12, 20…
http://gentlehugs.livejournal.com/38247.html
As a contribution to Fibromyalgia and Chronic Fatigue Syndrome Awareness Day, I would like to share my personal story with you. "It is my own personal experience and belief; FMS/CFS patients NEED to be a key player on our own team. WE need to continue
National Fibromyalgia Awareness Day -…
http://www.faithfamilyfibro.com/2010/05/…
National Fibromyalgia Awareness Day - How You…
http://www.faithfamilyfibro.com/2010/05/national-f…
Examples from the NFA on how everyone can make others aware of fibro. I am also asking my readers and bloggers to do something today for awareness. I have a Mr. Linky link up for those bloggers that write a post about fibro. I also have a giveaway for
For the fun of it by John Randolf Pric…
http://websie.com/post
For the fun of it by John Randolf Price
Live for the fun of it, and die for the fun of it. Nothing else really matters. Play more, for the fun of it; love and make love more, for the fun of it. Touch and hold and kiss the one who lights up your life, for the fun of it. Why look back with an
coyote587
OhMyAchesandPains
docmock
barbarany9
LiteraryNobody
kimberlyfr
Dominique
Ana
5/12/10 New to blogging
by: tydi0219
I am very new at this. I really wish that the health insurance companies or the hospitals would offer an excerise program for people that have FM & CFS..It is a big help but I believe you need to be helped through it. I was diagnosed with FM in 2004. It is very painful and the brain fog is terrible..
Read More Reply 0 comments