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No funding for MS drug.

  • 29-05-2014 7:56pm
    #1
    byhookorbycrook
    Moderators, Education Moderators, Regional South East Moderators Posts: 12,514 Mod ✭✭✭✭


    I wonder if the Ms-ers here have been on Fampyra, the only drug proven to help with walking in MS? I have found it wonderful, am far less stiff and sore, can actually do a day's work without having to sit all the time too.

    As of end of June, it will cost up to €500 a month, way beyond the reach of most people. It has been turned down by a "pharmo-economics" body who don't think it is worth the money!:mad::mad::mad::mad::mad::mad::mad::mad:


Comments

  • #2
    byhookorbycrook
    Moderators, Education Moderators, Regional South East Moderators Posts: 12,514 Mod ✭✭✭✭byhookorbycrook


    If anyone is on this drug, would you pm me please?


  • #3
    byhookorbycrook
    Moderators, Education Moderators, Regional South East Moderators Posts: 12,514 Mod ✭✭✭✭byhookorbycrook


    Lots of media interest ,campaign gathering speed.


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