Impact of MS-related fatigue on patients’ everyday life
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Hello everyone,
How are you doing today? 
I just wanted to let you know that second questionnaire on MS fatigue is available for you all! Have you had a chance to participate yet?
@hgrisar @Mayasmom @BillieDevore @hp2970 @Dianna67 @Candacelee12 @Mindyp8474pass @Rechel @bobbijean @Mastergoku55 @Nmg0908
Take care,
Courtney
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Courtney_J, Community Manager, Carenity US
Courtney_J
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Courtney_J
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Last activity on 08/08/2022 at 11:09 AM
Joined in 2020
1,340 comments posted | 96 in the Living with Multiple Sclerosis group
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Hello everyone,
We are currently conducting a large-scale survey for patients living with Multiple Sclerosis. The objective of this investigation is to assess fatigue-related symptoms and their impacts on the everyday life of adult relapsing MS patients.
We are very interested in understanding the impact of fatigue on the everyday life of MS patients. How much does fatigue-related symptoms impact patients’ life? What solutions do patients use to cope with fatigue?
Click here to share your experience
Your answers will provide precious insight into the burden of fatigue. Respondents will be compensated for their time, up to $50 if they respond to the full survey.
Have a great day,
The CarenityTeam