This is topic Long-COVID a lot like many other syndromes in forum General Support at LymeNet Flash.


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Posted by Razzle (Member # 30398) on :
 
Sounds a lot like Chronic Lyme...maybe this will start to open doctors' minds to the concept that Chronic Lyme exists and is not "all in our heads."

Long Covid isn’t as unique as we thought
https://www.vox.com/22298751/long-term-side-effects-covid-19-hauler-symptoms

Quote from the article: "The nagging symptoms long-haulers experience reveal a frustrating blind spot in medicine."
 
Posted by Lymetoo (Member # 743) on :
 
More:

https://www.nytimes.com/2021/01/21/magazine/covid-aftereffects.html?fbclid=IwAR2PZyMk16WJgzU-suys_iWm-Q5ORmu2TZ8sVJ-lnxEni7xTJI7LBhFQqpI

I think it will also help those who have MCAS.
 
Posted by marie (Member # 3980) on :
 
How come there are no centers for those who have "Post Lyme Syndrome". We are supposed to suffer without real support and validation.
 


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