ATTENTION CANADIANS:TIME TO PRESSURE FEDS.ME-CLIN/TRI

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.
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Gardenia
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ATTENTION CANADIANS:TIME TO PRESSURE FEDS.ME-CLIN/TRI

Post by Gardenia »

Whst the hell is going on in Canada? The Feds said they would fund clinical trials now what the f#ck is going on on this front when where who is doing double blinded clinical trials? Seems nothing -TIME TO SERIOUSLY START RAISING BLOOODY MURDER ON THIS FRONT-EVERYONE IS SERIOUSLY DRAGGING THEIR ASSES IN CANADA!!!!!
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fee001
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Post by fee001 »

Hi!

Dont get angry with me, but what trials are they not funding

Fiona
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Gardenia
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Post by Gardenia »

What they are doing so far in Canada from the provincial governments to the federal Harper government and dthe medical community is giving a lot of lip service-there's a little too much talk and no action.The same could be said in other countries. But there is such a high prevalence of MS in Canada that we should be take a LEAD here, PERIOD!!!!!!!
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Post by Cece »

When, where, and who are good questions.
It might take them time to get things started, it would be just as bad if they rush in with poor techniques or a poor trial design.
I think it is still very encouraging that they are taking things forward with clinical trials!
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munchkin
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Post by munchkin »

You are so right, but when the media. the Dr's, and many parliamentarians are trying hard to keep things quiet it's hard to keep the message going.
I have written letters to our minister of health, to the city paper and to specific reporters. Here in Winnipeg I'm told that there is enough information out there, people don't want to hear more.

It just gets so frustrating.
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fee001
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Post by fee001 »

Hi!

It's ok now. no :?: :?: :?: :?: :?: :?: longer in the dark, isnt the internet a wonderful thing.
I do my own research, and find my own answers Its good to talk
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