- to spread the truth about ME/CFS - that it is a biological disease, as scientific evidence shows, and not psychological in nature
- to end stigmatization and abuse of ME/CFS patients around the world
- to support people with ME/CFS and their families in every way we can
- to raise funds for real, useful biomedical research, so that causes and treatments and ultimately CURES can be found
Hope it helps x
*For all who read my blog, It would be amazing if you could forward my link http://dld.bz/mBZq to as many people as you know (twitter/facebook/your email list etc). You will then be doing your own bit for ME/CFS awareness and spreading the word to people who one day might just need it!* x
As some of you will already know I am a ME/CFS sufferer and have been for a couple of years now. I have decided to do as much work as my body allows me to do, trying to source helpful information and give my own experiences to generate Awareness to this disease. Today I just wanted to point you in the direction of a very informative website called WAMCARE. This site is a worldwide research association for ME/CFS, doing a great job creating awareness on this debilitating disease. Below Is a list of WAMCARE's goals along with their website link.
Julie and pete here :-)
The secret to finding Contentment, being positive and enjoying life!