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- What do you wish people knew about MS?
What do you wish people knew about MS?
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Senator
Senator
Last activity on 12/09/2020 at 3:29 PM
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3 comments posted | 2 in the Living with Multiple Sclerosis group
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Well put Candace. The big part I believe people don`t realize is the pain part. I get at times pain in my feet that is measured, by me, on a scale of 1 - 10, with 10 being most painful at an 8. I have PPMS which is the worst to have and am wheelchair bound. I try everything for pain including numerous pain medication that sometimes just doesn`t work all the time. I use the strongest CBD cream which can alleviate some of the pain. Best of luck on your journey.
Eistot
Eistot
Last activity on 10/21/2022 at 11:47 PM
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4 comments posted | 4 in the Living with Multiple Sclerosis group
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Not even my husband can comprehend. The pain is awful. Last week went to pain management they had so many I had to sit outside in the heat when they got to where I sign in at desk I passed out. Sure fire way to get in quicker
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Carole Beasley
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Courtney_J
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Courtney_J
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Last activity on 08/08/2022 at 11:09 AM
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Hello everyone,
If you don't already know, this week of March 8th to March 14th) is MS Awareness Week in the US! As MS is so complex and is an "invisible disease" (it's not always easily visible to others), many people know very little, if anything about it.
What are some things you wish people knew about MS?
The more people who are aware of MS, hopefully the sooner we will find a cure!
This discussion is yours to share your thoughts and opinions.
Looking forward to hearing from you all,
Courtney