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MS neurologist thinks injectable MS drugs should be taken off the market

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    MS neurologist thinks injectable MS drugs should be taken off the market

    Maybe Dr. Aaron Boster is trying to stir up controversy here. Here is a video he made (May 17, I think) arguing that the older injectable MS drugs should be taken off the market, just not offered any more:

    SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

    #2
    I agree with him, and my neuro might, also. MS is an aggressive disease and requires aggressive treatment.

    That said, I went off Rituxan at the start of the pandemic and went on Avonex. If tests show that I have made antibodies to covid, I will restart Rituxan next month.

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      #3
      I wonder what he would have to say to a person like me, who they say all the other drugs are dangerous for me.
      Virginia

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        #4
        He allows as how some people could stay on the injectable drugs but he also makes it clear that he'd prefer to see them out of the picture. I doubt that this will happen soon.
        SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

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          #5
          Of course there will be people who can't take the more aggressive drugs for various reasons.

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