Patients Multiple sclerosis
Topic of the discussion
Posted on 3/17/20 6:31 PM
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?
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,
Beginning of the discussion - 4/20/20Impact of MS-related fatigue on patients’ everyday life https://www.carenity.us/forum/multiple-sclerosis/living-with-multiple-sclerosis/impact-of-msrelated-fatigue-on-patients-everyday-life-1657
Posted on 4/20/20 6:14 PM
@Courtney_J Thanks for sharing the survey! If I can contribute to research and maybe progress for MS patients in any way I'll do it! I don't even care about the financial incentive!
Posted on 10/23/20 5:36 PM
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