What I wish the medical community would figure out for MS patients

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Elk217015

09/23/2022 at 1:41 AM

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Elk217015

Last activity on 01/01/2026 at 11:03 PM

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11 comments posted | 7 in the Living with Multiple Sclerosis group

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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

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LizziB

09/28/2022 at 6:00 PM

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LizziB

Last activity on 04/21/2024 at 8:17 PM

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603 comments posted | 35 in the Living with Multiple Sclerosis group

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Hi @Elk217015

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

Take care,

Lizzi

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LizziB

What I wish the medical community would figure out for MS patients https://www.carenity.us/forum/other-discussions/living-with-multiple-sclerosis/why-is-it-so-hard-one-day-not-the-next-4945 2022-09-28 18:00:17

What I wish the medical community would figure out for MS patients

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