Hi friends,
The National FMS - CFS Databases are ready!
These three databases are set up to better manage specific Governments so when including yourself be sure you choose the appropriate database for your residence either USA, Canada, or International.
We welcome your help to create a database for action and for researchers. Researchers have told us that they have to spend part of their research time and money on finding patients. We can help them change that by making it fast and free to fund us. If we assemble enough of us, we can make it possible to do large studies that were previously impossibly expensive.
http://fibrohugs.com/movement.html
Please help by adding the National FMS - CFS Database code to your web site so people will have multiple accesses to these databases. To be successful in accomplishing this goal, it will take everyone getting involved. One of the most important necessities is to fill these databases up as quickly as possible so we are recognized as "documented millions" rather than "just a bunch" of people with chronic pain. Besides the valuable resource this will be for Researchers to learn from the source (us), this will also be available for statistical purposes to better report extremely accurate numbers and percentages.
http://fibrohugs.com/movecode.html
When you successfully have the banner displayed on your site be sure to contact us at database@fibrohugs.com so that we can add you to the Participants page.
http://fibrohugs.com/movesites.html
Please get involved in the planning or just read what is happening this year on the Awareness Forum. This forum will also serve as a "help forum" for those that could use extra help in adding html code to their sites and so on.
http://fibrohugsforums.mysitemain.com/cgi-bin/webbbs/aware/index.pl
The best way that you can immediately help is to get this information out to everyone. Even if you are on a message board that discusses horses or construction, you have no idea how many readers of that board may have FMS or CFS. Please, and I can't stress this strong enough, ASK permission from the webmaster of any site you would like to post the information on. It's very important to do so in this respectable way. Thank you.
Check out these sites:
FM-CFS Canada http://fm-cfs.ca
The National ME/FM Action Network http://www3.sympatico.ca/me-fm.action
The National Fibromyalgia Partnership http://www.fmpartnership.org

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