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Commentary: When COVID-19 symptoms last for months, recovery feels slow and strained

Epidermologist Margot Gage Witvliet says she went from being healthy and active to fearing she was dying almost overnight – and dug into the research to understand what's happening to long-haulers like her.

Commentary: When COVID-19 symptoms last for months, recovery feels slow and strained

A woman in a face mask walks in the downtown area of Manhattan, New York City, after further cases of coronavirus were confirmed in New York, US, Mar 5, 2020. (Photo: REUTERS/Andrew Kelly)

BEAUMONT, Texas: Imagine being young and healthy, a non-smoker with no preexisting health conditions, and then waking up one morning feeling like you were being suffocated by an unseen force. 

Back in March, this was my reality.

I had just returned from Europe, and roughly 10 days later started having flu-like symptoms. I became weak overnight and had trouble breathing. 

It felt like jogging in the Rocky Mountains without being in condition, only I wasn’t moving. I went to the hospital, where I was tested for COVID-19.

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More than four months later, the symptoms have not gone away. My heart still races even though I am resting. 

I cannot stay in the sun for long periods; it zaps all of my energy. I have gastrointestinal problems, ringing in the ears and chest pain.

I’m what’s known as a long-hauler – part of a growing group of people who have COVID-19 and have never fully recovered. 

Fatigue is one of the most common persistent symptoms, but there are many others, including the cognitive effects people often describe as brain fog. 

As more patients face these persistent symptoms, employers will have to find ways to work with them. It’s too soon to say we’re disabled, but it’s also too soon to know how long the damage will last.

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What made matters worse in the beginning was that my doctors were not certain I had COVID-19. My test was negative and I had no fever, so my symptoms did not fit into early descriptions of the disease. 

Instead, I was diagnosed with a respiratory illness, prescribed the Z-pack antibiotic and a low dosage of an anti-inflammatory medication normally used for arthritis patients.

A Yale study released in May shows COVID-19 deaths in America do not reflect the pandemic’s true mortality rate. If I had died at home, my death would not have been counted as COVID-19.

By the end of March, I was on the road to recovery. Then I had a seizure.

A former coronavirus disease (COVID-19) patient who underwent lung transplant surgery, takes a remedial exercise at Hallym Sacred Heart Hospital ECMO Center in Anyang. (Photo: Reuters)

In the ER, the doctor said I had COVID-19 and that I was lucky – tests showed my organs did not have lasting damage. After the seizure, I lay in my bedroom for weeks with the curtains drawn, because light and sound had started to hurt.


I did not understand why I was not recovering. I began searching for answers online. I found a support group for people struggling with COVID-19 long-term. They called themselves long-haulers.

COVID-19 support groups show that there are many people not considered sick enough to be hospitalised – yet they are experiencing symptoms worse than the flu. It is possible COVID-19 is neurotoxic and is one of the first illnesses capable of crossing the blood-brain barrier. 

This might explain why many people like me have neurological problems. Many long-haulers are experiencing post-viral symptoms similar to those caused by mononucleosis and myalgic encephalomyelitis/chronic fatigue syndrome.

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A common frustration is that some medical doctors dismiss their complaints as psychological.

One woman in the support group wrote: “140 days later, so many are hard to breathe, and no doctors will take me seriously as I was diagnosed with a negative swab and negative antibodies.”

Paul Garner was the first epidemiologist to publicly share his COVID status. He described his 7-week fight with the coronavirus in a blog post for the British medical journal The BMJ.

That month, an Indiana University researcher working with an online community of long-haulers released a report identifying over 100 symptoms, and the US Centers for Disease Control and Prevention (CDC) expanded its list of characteristics that put people at greater risk of developing severe COVID-19 symptoms. 

On Jul 31, the US CDC also acknowledged that young people with no prior medical issues can experience long-term symptoms.

It’s still unclear why COVID-19 impacts some people more severely than others. Emerging evidence suggests blood type might play a role. However, the data is mixed.

A doctor wears a protective mask as he walks outside Mount Sinai Hospital in Manhattan during the outbreak of the coronavirus disease (COVID-19) in New York City, New York, U.S., April 1, 2020. REUTERS/Brendan Mcdermid/Files


Like many long-haulers, my goal is to resume a normal life.

I still grapple with a host of post-viral issues, including extreme fatigue, brain fog and headaches. I spend the majority of my day resting.

A big challenge long-haulers face may be sustaining employment. Ultimately, it is too early to classify long-haulers as having a disability. 

Anthony Fauci reported that “it will take months to a year or more to know whether lingering COVID-19 symptoms in young people could be chronic illnesses.”

Economics is a big driver of health, and the link between employment and health care in America further exacerbates the need to maintain employment to protect health. 

Employers need to be ready to make accommodations to keep long-haulers working. The stress of being sick long-term, combined with the possibility of job loss, can also contribute to mental health issues.

To effectively fight COVID-19 and understand the risks, these patients with continuing symptoms must be studied. Online support groups, meanwhile, are helping long-haulers feel understood.

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Margot Gage Witvliet is Assistant Professor of Social Epidemiology, Lamar University. This commentary first appeared on The Conversation.


Source: CNA/sl


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