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Mental Health Co-Morbidities in MS

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    #1

    Mental Health Co-Morbidities in MS

    I had the privilege of attending the Consortium of Multiple Sclerosis Centers annual meeting in Seattle last week where 2200 Clinicians from around the world met to share research, rehab, treatment plans with each other. Friday (5/31/2019) my day was spent in sessions related to Mental Health and MS. Real Talk MS did a podcast each day and Friday's starts with my recount of the sessions I attended. I speak for about 12 or 13 minutes at the start of this half hour podcast. Only registered and activated users can see links., Click Here To Register...

    If you wish to listen to more podcasts about MS go to Only registered and activated users can see links., Click Here To Register...
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    #2
    Thank you Cherie, I did listen to what you posted and enjoyed hearing a few minutes of what went on. Good job.
    Virginia

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      #3
      Very instructive! Interesting that people with MS have two and a half times as much stress as other people. I can certainly believe that.

      I'm not very knowledgeable about podcasts and so was probably doing something wrong but I couldn't get past the first couple of minutes of it in the link. However, I found it using the RealTalk link you provided and was able to hear it quite well.
      SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

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        #4
        thanks Cherie, i just listened to your very effective presentation— you seem to have the cognitive skills and a voice of a much younger woman!!! The info was valuable. Am especially interested in the Telemedicine comments.

        For me, I know longer can get to many of my docs without help. its a 30 minute drive, and then, at the end of the drive, its too far to walk from the hcap space to the building where the wheelchairs are. telemedicine would be a great alternative when i cant find a ride.

        The statistics on MS mental health issues, I wonder how it compares to other serious neuro disorder. Might the depression, anxiety and sucide rates be equivalent. Or compared to other non neurological but serious illness patients. Same questions? I.e. is it the MS per se, or is it the difficulty in living with this type of condition...

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          #5
          I was so very, very tired by the time of this interview that I felt like my speaking was in slow motion and I sounded "blotto" but as we moved through it, I think I "woke up " a bit. I appreciate your kind words and support.

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            #6
            Originally posted by Cherie View Post
            I was so very, very tired by the time of this interview that I felt like my speaking was in slow motion and I sounded "blotto" but as we moved through it, I think I "woke up " a bit. I appreciate your kind words and support.
            It may have felt like that, but from what I heard, the audience would not have thought you sounded blotto etc!

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