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CAN YOU MAKE A DONATION TO Chronic Fatigue and Immune Dysfunction Syndrome RESEARCH? Learn More Here.

Posted by Catherine Morgan on April 4, 2007

I found a site today at The CFIDS Association of America, that enables anyone to make a fund raising page for Chronic Fatigue Syndrome. So, I went ahead and made one. If you would like to see it or donate, click here.

Join me in my efforts to support the CFIDS Association of America!

If you are able to donate, thank you very much. If you are unable to donate at this time (as I am)…..please consider sending this post to any friends or family that you think may be able to. Thank you very much.

If you would like to make your own page to raise money for Chronic Fatigue Syndrome, you can go to the My Cause page of the CFIDS website. It is very quick and easy to do, and when you are finished it gives you a way to add email addresses in order to send the link to your friends and family.

For more information on Chronic Fatigue Syndrome go to Living With Chronic Fatigue Syndrome.

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This video was made specifically for the family and friends of people suffering from Chronic Fatigue Syndrome and related conditions. You can go to the SLEEPYDUST.NET web-site and use a link to send this video via Email to as many people as you would like. The more people that understand and have compassion for this disease the better. There are also two videos that are talking about Fibromyagia (FM).

[YouTube=http://www.youtube.com/watch?v=r0w9-eQ_fKQ]

ALSO SEE:

INFORMATION ON CFS THAT YOU CAN PRINT OUT AND GIVE TO YOUR DOCTOR, WRITTEN BY DOCTORS, FOR DOCTORS.

SEVERAL VIDEOS THAT EXPLAIN CHRONIC FATIGUE SYNDROME, YOU CAN PASS THEM ON TO FRIENDS AND FAMILY.

TIPS FOR LIVING WITH CHRONIC FATIGUE SYNDROME.

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3 Responses to “CAN YOU MAKE A DONATION TO Chronic Fatigue and Immune Dysfunction Syndrome RESEARCH? Learn More Here.”

  1. […] CAN YOU MAKE A DONATION TO Chronic Fatigue and… […]

  2. helenl said

    Hi Catherine, What a great video. I have two poet friends who have CFS. I will try to encourage them more.

  3. Hi Helen. Thanks for the comment, I’m sure your friends will appreciate your additional encouragement. A few weeks ago I started a site specifically dealing with CFS and FM. You might be interested in this post…

    http://livingwithcfs.wordpress.com/2007/03/23/helpful-information-from-the-cdc-for-family-friends-and-physicians-of-patients-with-chronic-fatigue-syndrome-cfs-fm/

    and this is a page on the site that I have about six different videos that address CFS and FM….

    http://livingwithcfs.wordpress.com/videos-explaining-cfs/

    Thanks again.

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