Researchers at Trinity College Dublin are developing online resources for people affected by multiple sclerosis. Everything they develop will be made freely available to the general public.
They are looking for people living with MS, people who work with them, and their relatives, friends and loved ones to complete a survey in order to get their input and learn from their experiences.
The survey can be accessed here: https://www.surveymonkey.com/r/TCD_MS_UK
Thank you in advance - your participation will be invaluable in helping them to create the most relevant, useful and engaging content possible!
P.S. This survey includes questions about MS. If you need to talk afterwards, remember the MS-UK Helpline is here for you. Just call 0800 783 0518 or visit http://www.ms-uk.org/helpline
Multiple Sclerosis Survey
Multiple Sclerosis Survey
MS-UK - http://www.ms-uk.org/
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euphoniaa
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Re: Multiple Sclerosis Survey
FYI - I believe it's the same survey that was given in this thread on January 23: http://www.thisisms.com/forum/general-d ... 27286.htmlMSUK wrote:Researchers at Trinity College Dublin are developing online resources for people affected by multiple sclerosis. Everything they develop will be made freely available to the general public.
They are looking for people living with MS, people who work with them, and their relatives, friends and loved ones to complete a survey in order to get their input and learn from their experiences.
The survey can be accessed here: https://www.surveymonkey.com/r/TCD_MS_UK
Thank you in advance - your participation will be invaluable in helping them to create the most relevant, useful and engaging content possible!
P.S. This survey includes questions about MS. If you need to talk afterwards, remember the MS-UK Helpline is here for you. Just call 0800 783 0518 or visit http://www.ms-uk.org/helpline
I liked the way the survey was done, so I'll bump that thread, too.
Dx'd with MS & HNPP (hereditary peripheral neuropathy) 7/03 but must have had MS for 30 yrs before that. I've never taken meds for MS except 1 yr experiment on LDN. (I found diet, exercise, sleep, humor, music help me the most.)