Society Logo
ME/CFS Australia Ltd
Please click here to donate ME/CFS South Australia Inc
 
 
Facebook
 
ME/CFS SOUTH AUSTRALIA INC

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)

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.

Become a Member
DOCX Application Form (Word, 198 KB)
Why become a member?

'This Is Real': COVID-19 Long-Hauler's Months Of Agony

Sunday 12 July 2020

 

From Agence-France Presse (via Yahoo! News):

 

Scott Krakower
Scott Krakower, a psychiatrist, poses in front of his home
in Port Washington on Long Island, New York.
 

'This is real': COVID-19 long-hauler's months of agony

By Issam Ahmed
Agence-France Presse
11 July 2020
Copyright © 2020 Agence-France Presse / Yahoo! News.

Child psychiatrist Scott Krakower tested positive for COVID-19 back in mid-April, but three months on there are still days he feels overwhelmingly tired, short of breath, and unable to speak because of a hoarse throat.

The 40-year-old New Yorker is among a wave of patients being referred to as "long-haulers," whose recovery period extends far beyond the two or so weeks that are the average length of the illness.

He told AFP there are days he encounters "self-skepticism," wondering if the symptoms he's going through are real and he should be back at work -- until, for example, he takes a walk and his parents or wife who are on the phone with him notice he's gasping.

This phenomenon is attributed to a mysterious post-viral illness that is still poorly understood -- but increasingly reported by patients, who are sharing their experiences online in forums like the Long Covid Support Group on Facebook with more than 5,000 members.

"Just when I think I'm on a roll and have like three or four good days, I'll have about three or four hours where again I can't speak or my lymph node starts swelling on the right side of my neck," Krakower said in a video interview from his home in Long Island.

 

Full article…

 


 

blog comments powered by Disqus
Previous Previous Page