Count ME In for ME/CFS

Click here to donate: http://wpinstitute.org/help/help_donation.html

Count ME in is a worldwide Research Fund Drive established by ME/CFS forums (http://www.mecfsforums.com/index.php/topic,6210.0.html). It is a way for ME/CFS patients to fund quality biomedical research that the federal government is currently unwilling to provide.

We are tired of waiting for clear diagnostic criteria for ME/CFS.

We are tired of waiting for better physician knowledge and treatment of ME/CFS.

The WPI has already found a retroviral link (XMRV) to ME/CFS and has published these findings in one of the most prestigious medical journal/magazine Science. Since then, negative research papers that fail to properly replicate the WPI's original paper abound. Perhaps if these research organizations didn't have their pockets full of federal dollars it might be a different story. There is only one way to find out:

We need to fund our own research! We cannot wait for the government to do it for us!

This is a world wide fund drive because ME/CFS is a disease affecting 17 million people worldwide!

You can make a difference today!

Go to http://wpinstitute.org/help/help_donation.html to donate to the WPI and fund ME/CFS research for a better tomorrow for all ME/CFS sufferers!

**It has recently come to my attention that there are some ME/CFS sufferers who are so crippled by illness and poverty that they cannot make the minimum monthly dollar donation. I would like to honor these ME/CFS patients for their courage in battling this illness. It is not just for us, but for them we give!**

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Nonprofits & Activism

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