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Phoenix Rising ~ Interview With Dan Moricoli, a CFS/ME Patient


This is the face of CFS. Dan Moricoli owned his own business and for hobbies, he raced motorcycles, went deep-sea fishing and enjoyed being a skiing enthusiast. But CFS/ME changed his life.

The face of CFS:

http://aboutmecfs.org/blog/

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Avatar universal
Oh boy, go I agree. I hope one day some of these people who claim we are calling foul gets there's. I think what rials me more than anything is hearing "its' all in your head", theirs nothing wrong with you.
junglejim46
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Avatar universal

And all of these "mystery" autoimmune diseases and "syndromes" all involved the central nervous system.

It is going to be a great day for us. I hope those _________s who mouthed off about how these conditions were all in the head (stupid theory ---- do you really think these clusters of CFS in Lake Tahoe and New York were all made up?) will think twice before they abuse again.
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Avatar universal
Finally!!!!  Someone who understands and knows what is going on...truly knows.  I can not wait until their research is made public...what a GREAT day that will be as it will finally shut down those who continue to mock and disbelieve these illnesses.
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Avatar universal

More CFS & Fibromyalgia in the News today as well ! Check out Annette Whittemore and one of the physicians, who is researching these illnesses and fighting hard to come up with better testing and treatments for these often disabling diseases:

http://www.nevadanewsmakers.com/video/nnmstreamm.asp?showID=816
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