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What I wish the medical community would figure out for MS patients
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Thank you for your comment. I think everyone in this group would agree that there is not enough for MS patients.
What would be the first thing you wish the medical community would figure out for MS patients?
I'll tag a few members who may have opinions on this topic to get the discussion going.
@khuether @amboygirl29 @Pistachio @Truddell02 @Jme12Jme @Irishsuly @Jleakg01 @Sarah1004 @PSam96 @Solrick2017 @marlaro @Lynnmo @Racquel25 @dionisa71 @AMWood @Kimtraore @Relle100 @lpiquette @eigna728 @Amperage @WILLIAMSJANET @blehn9042
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I just feel we as MS Patients are tired of feeling ALL the pain and there isn't enough out there to help! Maybe for a short time