Lyme vs Long COVID: The Overlap Doctors Need to See
Lyme Science Blog
Dec 09

Lyme vs Long COVID: The Overlap Doctors Need to See

Comments: 2
2
Visited 1851 Times, 3 Visits today

When Lyme vs Long COVID Feels Impossible to Tell Apart

“Is this Lyme… or long COVID?”

Patients ask me this with a mix of fear and exhaustion. They describe the same constellation of symptoms — the brain fog that makes conversations feel slippery, the dizziness that hits out of nowhere, the heart that races as if the body is in danger, the fatigue that wipes out entire days.

Some became ill after COVID. Some after a tick bite. Many never saw a defining moment at all.

And that’s the challenge: the Lyme vs long COVID overlap is so significant that patients often find themselves dismissed, bounced between specialists, or told contradictory stories about their own illness.

Many describe feeling trapped between identities — not knowing whether Lyme, long COVID, or post-COVID symptoms explain the sudden unraveling of their health.


What the Research Shows About This Overlap

The patterns are not imagined.
They are documented.

The study Long-term neurologic outcomes of COVID-19 by Xu, Xie & Al-Aly demonstrated significantly higher rates of memory problems, slowed thinking, and difficulty concentrating in long COVID — symptoms identical to what I see in many Lyme patients.

And in my own published research, we compared individuals with a history of Lyme disease to those who later contracted COVID-19 or received the COVID-19 vaccine. The overall symptom burden did not significantly worsen after infection or vaccination, but about one in five who contracted COVID-19 went on to report long COVID.

That finding alone shows how intertwined Lyme vs long COVID can be.
Cameron & McWhinney, Antibiotics, 2023


Where the Symptoms Converge

Brain Fog That Steals Sharpness

Patients from both groups describe the same cognitive struggle: the conversation that slips away, the tasks that suddenly feel too complicated, the words that disappear mid-sentence. Some call it “post-COVID brain fog,” others describe it as part of their Lyme journey — but the lived experience is eerily similar.

A Nervous System That Misfires

Dysautonomia ties Lyme vs long COVID together more than almost anything else.
Dizziness, heart palpitations, faintness, temperature swings — symptoms that mimic anxiety but aren’t driven by emotion. They arise from the autonomic nervous system losing its stability.

Fatigue That Feels Like a Crash, Not Tiredness

Both conditions produce a unique kind of exhaustion: the sudden collapse after a small effort, the days-long setback, the “wired but tired” state. Patients learn to fear exertion because even minor activity can push the system into shutdown.

Pain That Takes Many Forms

Headaches, nerve pain, muscle aches — Lyme may migrate while long COVID pain often stays fixed, but both can disrupt daily life with striking similarity.


The Pattern Most Doctors Miss: Cycling Symptoms

One of the strongest diagnostic clues in Lyme vs long COVID is the waxing and waning of symptoms.

Patients describe days where they feel nearly normal, followed by sudden crashes of dizziness, exhaustion, or cognitive fog. This fluctuation is often misread as stress or recovery — when in reality, it’s a defining feature of both illnesses.

In each condition, symptom cycling is not a sign of imagination or instability.
It is a hallmark of the underlying biology.


Why the Lyme vs Long COVID Confusion Happens

Most doctors are trained to look for illnesses that follow consistent, predictable patterns. Lyme and long COVID rarely do. Instead, their symptoms rise and fall, move from one system to another, and evolve over months or even years. Patients might have a normal exam one week and feel incapacitated the next. Their labs may look reassuring, even when their day-to-day life is anything but.

Because these illnesses don’t behave the way clinicians expect, many patients end up hearing explanations that never quite fit. They’re told they’re anxious. They’re told it’s simply “post-viral.” They’re told it can’t be Lyme without a rash, or long COVID if their original infection was mild. None of these assumptions match the lived reality of what patients are experiencing.

And so they land in a kind of diagnostic limbo — sick enough to lose pieces of their life, but not “sick enough” in ways the medical system easily recognizes. The overlap between Lyme vs long COVID becomes the blind spot where many patients disappear.


Patients Deserve a Better Way to Understand Lyme vs Long COVID

Both Lyme disease and long COVID — including persistent post-COVID symptoms — are post-infectious neuroinflammatory illnesses. Both can disrupt brain function, autonomic regulation, immune balance, and energy systems.

Patients shouldn’t have to choose the “right” label to receive care.They need clinicians who recognize the shared patterns and are willing to look deeper than a single test result.


If You’re Trying to Understand Your Own Overlap

You’re not alone. I hear from people every day who feel caught between Lyme vs long COVID, uncertain which path their illness followed — or whether it followed both.

Your symptoms make sense. The overlap is real. And there are answers.


Are you trying to understand your own Lyme vs long COVID symptoms?

Share your experience — your story may help someone else find clarity.


Resources

  1. CDC. Long COVID Basics
  2. Pubmed. Long-term neurologic outcomes of COVID-19
  3. Dr. Daniel Cameron: Lyme Science Blog. Lyme, Long COVID, or Both? Making Sense of Persistent Symptoms
  4. Dr. Daniel Cameron: Lyme Science Blog. Is it Long COVID or Lyme disease?

Related Posts

2 thoughts on “Lyme vs Long COVID: The Overlap Doctors Need to See”

  1. I am a 72 yr old married female who had a mild case of Covid in October 2022. We (my husband and I) had taken the Covid-19 vaccinations after the infection. We got along afterwards very well and have had no Covid vaccinations since! I was diagnosed with Parkinson’s Disease in 2012 by a UNC-Ch movements disorder neurologist, Dr Nina Browner, MD. She had me in top shape and ready to do anything I needed to do. Life was good on the farm…until Sept/October, 2023. I was taken to local hospital where every medical test that could be done was done, but labs said I was normal. At this point, I was totally out of it! I lost almost 5 months of my life. I lost my memory, I couldn’t walk, talk, communication was very limited, food was a foreign forkful of mush so I would not eat! I was moved to ECU Health in Greenville where I stayed for 7-9 more days. I saw a hospital neurologist ONCE. He read my chart and saw the PD diagnosis, looked at my husband and said, “she has Parkinson’s”, turned and walked out never to be seen again. I was still incapacitated and had to be cared for by my husband and 2 grown sons while in the hospital. I didn’t communicate, so somebody had to stay with me to make sure my PD meds particularly were given. They sent me home with NO DIAGNOSIS and said I needed home health! I was unloaded by the ambulance EMTs put in my bed and they left! The drs at the local level hospital had already tested for everything imaginable, so they fell into trying to rehab me and get home health involved. My men were caught in something they never thought possible. Hospital said put me in a rehab, my family refused, and hired a wonderful lady to help me for what lay ahead! All of this information was told to me by my husband and sons over the course of almost a year! There’s still things coming out that I’ve never heard before!
    I never was offered a Lymes test until February 2024. We had to request it be done. It was a weak positive, but it was the first positive anything I had gotten in the last 6+ months! I started Doxycycline that very day.
    I could feel a difference within 3rd day! I was getting better! And without very much help from the medical community I’ve been going to all my adult life! No one will even acknowledge the test. All I have heard repeatedly is “ we don’t have that tick here”! One exception is my PD neurologist, Dr Browner. I wouldn’t have gotten this far without her guidance and caring. I love her!
    So much has happened since that day, Feb 28, 2024. There’s not enough time nor paper to put it on.i can tell you that it’s one of the hardest things my family has had to do for me. I praise the Lord for every day He gives me with my family. But “ it ain’t over till the fat lady sings”. I am still fighting and the farther I get, the more I find out there’s not a Dr in eastern NC who even wants to hear about Lymes much less treat you! I’ve been digging thru the internet for years only to find out that there’s help available but it’s far away, expensive and not very reliable nor helpful because distance is a major factor. I have been reading nearly all of Dr Cameron’s posts and blogs and see myself in nearly every one of them. Today, the blog introduced me to the link between COVID and Lymes. Add to that Parkinson’s Disease, that was once believed to be handled, isn’t !! I need help from somebody! I am a shell of who I used to be. My life is much smaller. The brain fog and inability to properly comprehend things, stops me from driving. Memory is horrible and I lose myself in a conversation about midway! I have uninvited relapses and not much ammunition to fight them! This is just the tip of the iceberg, Dr Cameron. I need some help and my husband of 53 yrs and 2 sons (51 &48) need help to at least be comforted that I’m heading in the right direction. Thank you! Benita Wells

    1. Dr. Daniel Cameron
      Dr. Daniel Cameron

      I an sorry to hear how tortuous your journey has been. I have Lyme disease patients share similar stories. Keep working on an answer for you and your husband

Leave a Comment

Your email address will not be published. Required fields are marked *