By Russell Fleming in The ME Association.
We are excited to announce a new international research study 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.
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