The ME Association #CountMEin Survey for everyone who might have symptoms or a diagnosis of ME/CFS and/or Long Covid in the UK,,Channel Islands, and the Isle of Man,
‘Count ME In’ - M.E. charity calls for an end to NHS neglect!
The campaign will run during 2023 and the ME Association’s (MEA) will share the survey outcomes which will be produced in December.
The MEA Reminder -
Count Me In Campaign Survey
More than 6000 people with either symptoms or a diagnosis of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome or Long Covid have already completed our Count Me In survey.
Help the ME Association create a true picture of life in the UK, so you can get the support you need.
Complete our survey and tell us how ME/CFS and Long Covid affects people like you.
For further information, see our previous blog.
ME Association #CountMEin survey & campaign
• M.E. Association
‘Count ME In’ - M.E. charity calls for an end to NHS neglect!
The campaign will run during 2023 and the ME Association’s (MEA) will share the survey outcomes which will be produced in December.
The MEA Reminder -
Count Me In Campaign Survey
More than 6000 people with either symptoms or a diagnosis of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome or Long Covid have already completed our Count Me In survey.
Help the ME Association create a true picture of life in the UK, so you can get the support you need.
Complete our survey and tell us how ME/CFS and Long Covid affects people like you.
For further information, see our previous blog.
ME Association #CountMEin survey & campaign
• M.E. Association
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