New International Research Study
We are excited to announce a looking at the impact of ME/CFS on the quality of life of both patients and their family members.
This is a short and simple online survey designed to be accessible to all adults 18+, including severely affected patients.
There are two questionnaires in the survey, one for the patient and one for a life partner or family member. If you cannot be together to complete it, you can save and return. People with ME/CFS piloting the survey found each questionnaire only took about 5 minutes to complete.
Please use the link: https://redcap.link/MECFSFamilyImpactStudy
Please share widely to encourage others to participate. The greater the reach of this survey the more we can improve international understanding of how ME/CFS impacts patients and their family members.
Thank you and best wishes,
Dr Nina Muirhead and the Study Team at Cardiff University, United Kingdom.