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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


From UK news outlet Metro:


Jason Reed
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

By Laura Abernethy
Saturday 18 April 2020
© 2020 Associated Newspapers Limited.

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.


Full article…



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