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Saturday, December 4, 2010 5:17 PM | CCSVI in MS Toronto Volg link

Here is a letter from a Canadian Neuro who received precious funding from the MS Society, to study CCSVI. I bet their study will be a big fat hoax, used to discredit CCSVI and everyone who supports it.

Obviously this Doctor from Neuroland is having great difficulty dealing with a medical paradigm shift of global proportions.

He's also a member of the MS Society Medical Advisory Committee.

What a complete disgrace...

Friday December 3 2010

"Dear (- - - - - - )

I'm very disappointed that you would join this mass hysteria movement based on unfounded facts that has led to no less than a cult, stoked by media who are loving the reaction of people feeding them with endless material. What if research shows, as it appears to be doing, that veins of MS patients are no different than anyone else's? Should we all go trying to alter our 'normal' anatomy? Is there no lesson learned from the now famous tragic death of the Costa Rican man who refused the advice of his doctors a) to not have the procedure and b) not to try to unplug it?

But who am I to question the word of the many self-acclaimed experts who feed this frenzy like the rock doctor Embry whose lifelong study of lifeless objects has given him the wisdom to comment on such complex issues?

I'm happy to discuss this with you anytime (- - - - - - ), but why you or any other of the cult members believe that I have influence over the government is beyond me. Our system supports evidence-based medicine. To do anything else would destroy it. Thus far the evidence simply does not support the theory of CCSVI regardless of the seemingly countless anecdotal reports.

But then, what do I know about such things?"

Ashton Embry - Different Approaches to the Application of Science to Understanding and Treating MS – An Open Letter to Mark Freedman:

http://www.facebook.com/note.php?note_id=175318079164366