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Review: MS Wars — Hope, Science and the Internet

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.

Review: MS Wars — Hope, Science and the Internet

Postby dania » Mon Feb 13, 2012 4:14 pm

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Re: Review: MS Wars — Hope, Science and the Internet

Postby jackiejay » Mon Feb 13, 2012 5:03 pm

I guess we know this guy''s opinion..."we already know part of the harm; the hopefully temporary derailment of genuine research and the search for therapies that work".....and the icing on the cake,this condescending statement...." tragic situations that bring people to irrationality"......
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Re: Review: MS Wars — Hope, Science and the Internet

Postby Billmeik » Wed Feb 15, 2012 7:29 pm

I would say the jury is still out as to whether this diversion in thought about MS has been justified.

I do think it should be illegal to mention Doepp's 0% paper from 2 or 3 years ago without mentioning his total turnaround(if I remember rich) this year.

Also mentioning zivadinof's 56% paper without mentioning his 2011(12?) paper where he found 80% is wrong.


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Re: Review: MS Wars — Hope, Science and the Internet

Postby 1eye » Wed Feb 15, 2012 11:21 pm

I encourage you to look at the insiders comments, which might require you to "register". There I meet the review's author in a drawn out discussion which I finally had to leave, because he got too long-winded. It follows the party line, as written by you-know-who: placebo, remissions, waste of research dollars, no evidence, etc..
"Try - Just A Little Bit Harder" - Janis Joplin
CCSVI procedure Albany Aug 2010
'MS' is over - if you want it
Patients sans/without patience
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