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MS patients attending conferences like ECTRIMS?

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    MS patients attending conferences like ECTRIMS?

    There are people who believe that MS patients should be allowed to attend the big neurology conferences relevant to MS, like the recent ECTRIMS conference in London.

    Only registered and activated users can see links., Click Here To Register...

    Since I have MS to the point where travel is next to impossible, I wouldn't be going anyway but just wondered how others feel. Would this be useful? Would it be a good way to find information?

    My opinion is that it definitely wouldn't but that's just my opinion.
    SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

    #2
    I agree with you. And, it could interfere with collegial exchanges between doctors and researchers. I am glad though that they make the abstracts available.

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