FM/CFS/ME RESOURCES - Welcome Letter
 



 




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 WELCOME LETTER

Welcome

Dear Visitor,

FM/CFS/ME RESOURCES is here solely to inform and assist patients, caregivers, and families living with Fibromyalgia and Chronic Fatigue Syndrome/Myalgic Encephalopathy (CFS/ME). On this website you'll find a multitude of resources including attorney, doctor, drug, disability and support group information to enable you to take control of your illness. My ultimate goal is to find a cure. Together, with the help of others like you, I'm certain a cure will be found!

Background

In the summer of 1978, at the age of 18 years old, I became sick with FM and CFS/ME. I spent the next ten years going to doctors of every specialty before I was properly diagnosed. Once I had my diagnois I searched for anything I could find about these disabling medical conditions. However, back in 1988 there was very little known or written about FM and CFS/ME.

Over the next 9 years I worked hard to learn all I could about FM, CFS/ME, how to use a computer, and how to make a web site. In the fall of 1997 FM/CFS/ME RESOURCES was created to provide support, education, and informational resources to patients, caregivers, and families living with FM and CFS/ME to live a better life.

Objectives

The first objective of FM/CFS/ME RESOURCES is to assist in finding the cause and cure for FM and CFS/ME. By taking the FM/CFS/ME Survey, you are helping to reach this goal. The second objective is to inform and assist patients, caregivers, and families living with FM and CFS/ME to take control of their illness. FM/CFS/ME RESOURCES has been providing accurate medical information related to FM and CFS/ME since 1997.

Content

The What's New option is your first stop for news and updates regarding FM, CFS/ME and this web site. The FAQ's option answers many commonly asked questions concerning FM, CFS/ME and Pediatric CFS/ME. The Search Site option enables you to easily find any information within this web site. Our Basic Resources contain references that will enable you to learn more about your illness. The Support Group resources contain In-person and Online support group information, along with instructions on how to List Your Group with us, information on how to Start A Group of your own, and articles such as Getting The Most From Support Groups. I also have a new section entitled Family & Friends. This page contains information that explains what you're experiencing, helping your family and friends to better understand you and your illness. Help me to improve this site by taking the visitor survey.

Feel free to Contact me with any questions or comments you might have. I sincerely hope that you find this site useful.

You're Not Alone,

Signature

Owner - Patient
FM/CFS/ME RESOURCES

Misty Roberts
March
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