Invisible Illness CFIDS/FMS

Allow yourself to share your experience with this invisible illness and help yourself and others too. Share your tools, how you deal with everyday life, and gain access to information on Chronic Fatigue and Immune Dysfunction Syndrome and Fibromyalgia (CFIDS/FMS). My mission is to empower patients to take control of their health by providing my own story and experience with treatment information, quality health products, community, and advocacy.

Tuesday, June 24, 2008

Dropping a Note to Say Hello

›
Hello My Dear Readers, I have been very busy with my dear husband chronically ill with COPD. He has been in and out of the hospital and thi...
2 comments:
Monday, May 05, 2008

Just a note-found a site on "Disability"

›
Hello Everyone, I am sorry I have not written anything lately. However, I was notified abou...
4 comments:
Thursday, February 28, 2008

Are you Credible?

›
Hello Everyone, I have not posted for awhile. I thought I would just write a few words about credibility. I started off with my title: Ar...
11 comments:
Monday, February 18, 2008

Cheer You Up Award

›
Hello Everyone! I just started to look at some sites and noticed I was awarded the You Cheer Me Up Award! Wow!!! I know there are many blog...
8 comments:
Friday, February 08, 2008

Hello Everyone!

›
Sorry I've been away, I have been dealing with the flu and when you have fms/cfs, the symptoms are a million times worse! You know what...
Wednesday, January 09, 2008

The Consequence of Chronic Stress

›
Hello Everyone, I feel the need to take the time to post something today because I believe it is very important to keep this information on ...
2 comments:
Friday, November 30, 2007

I wanted to mention new site and friends

›
These pages I joined a new community in November and met some very nice people. I wanted to mention their sites and ask that you please che...
2 comments:
‹
›
Home
View web version

About Me

View my complete profile
Powered by Blogger.