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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.
Disclaimer
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.
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My Quarantine Routine: Jason, Who Lives With M.E. And Has Been Housebound For Most Of His Life
Sunday 19 April 2020
 Jason is working on a new podcast about isolation. (Picture: Jason Reed) |
My Quarantine Routine: Jason, who lives with M.E. and has been housebound for most of his life
Lockdown seems unusual and difficult for most of us and we’re used to being out and about.
But for many disabled people, spending most of their time at home is how their lives have been for a long time.
Today for My Quarantine Routine, we’re with Jason Reed, 40, from Sittingbourne, Kent.
Jason has my myalgic encephalomyelitis (ME), which is also known as chronic fatigue syndrome (CFS).
Having lived with the condition for 30 years, he has been housebound for most of his life.
He says that the outbreak of coronavirus could help disabled people in some ways as things are more accessible remotely and people understand more about what it is like to live in isolation all the time.
During this time, Jason has launched a new podcast called So I Start A Revolution From My Bed about living in isolation and being housebound.
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Registered Charity 3104
Email:
sacfs@sacfs.asn.au
Mailing address:
PO Box 322,
Modbury North,
South Australia 5092
Phone:
1300 128 339
Office Hours:
Monday - Friday,
10am - 4pm
(phone)