ME/CFS South Australia Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members.
ME/CFS South Australia Inc aims to keep members informed of various research projects, diets, medications, therapies, news items, etc. All communication, both verbal and written, is merely to disseminate information and not to make recommendations or directives.
Unless otherwise stated, the views expressed on this Web site are not necessarily the official views of the Society or its Committee and are not simply an endorsement of products or services.
Two South Australian ME/CFS Surveys
Thursday 17 September 2020
Update and Thanks: Researcher Amy Hill has asked us to thank everyone who has participated in the surveys so far. However, very few people have participated in the carer's survey. To participate in the carer's survey, please note that this can include parents, spouses and other family members, not just paid care staff.
From researcher Amy Hill:
To whom this may concern,
My name is Amy Hill, a year 11 student.
I am currently doing my SACE Research Project on ME/CFS, and have written two surveys.
They are designed to take less than 10 minutes each.
Survey 1 (for ME/CFS sufferers):
Survey 1 is only for people clinically diagnosed with ME/CFS.
You may have Fibromyalgia as well, but not Fibromyalgia only.
The link is: https://www.surveymonkey.com/r/ZBHNXWQ
Survey 2 (for ME/CFS carers):
Survey 2 is for carers and family of ME/CFS sufferers.
The link is: https://www.surveymonkey.com/r/M5D7YYZ
I appreciate your time.
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Registered Charity 3104
PO Box 322,
South Australia 5092
1300 128 339
Monday - Friday,
10am - 4pm