WHY AM I GETTING WEAKER IF MY TESTS ARE NORMAL
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Jan 29

ALS and MS suspected in woman later diagnosed with Bartonella and Lyme disease

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Diseases That Mimic ALS: Can Lyme Disease or Bartonella Be the Cause?

Several neurological disorders and infections can produce symptoms that resemble amyotrophic lateral sclerosis (ALS). Progressive muscle weakness, gait abnormalities, balance problems, muscle pain, and other neurologic symptoms often prompt an evaluation for ALS, multiple sclerosis (MS), or other neurodegenerative disorders. In some patients, however, an underlying infection such as Lyme disease or Bartonella may contribute to the clinical picture.

Most people evaluated for ALS do not have Lyme disease or Bartonella infection. Nevertheless, these infections occasionally produce symptoms that overlap with ALS or MS and should remain part of the differential diagnosis when exposure history, systemic symptoms, or other clinical findings raise suspicion.

In their article, Bartonella- and Borrelia-Related Disease Presenting as a Neurological Condition Revealing the Need for Better Diagnostics, Ericson and colleagues describe a woman whose illness evolved over several years before specialized testing identified both Bartonella infection and Lyme disease.1

What diseases can mimic ALS?

Several neurological and systemic disorders may resemble ALS during the early stages of illness. Depending on the patient’s symptoms and examination, physicians may consider infectious, inflammatory, autoimmune, metabolic, or structural neurological disorders before confirming a diagnosis of ALS.

Potential ALS mimics include:

  • Lyme disease
  • Bartonella infection
  • Multiple sclerosis (MS)
  • Multifocal motor neuropathy
  • Cervical spinal cord disease
  • Vitamin B12 deficiency
  • Inflammatory neuropathies
  • Other infectious or autoimmune neurologic disorders

Because several of these conditions are potentially treatable, identifying the correct diagnosis is essential.

Can Lyme disease mimic ALS?

Neurologic Lyme disease may occasionally produce symptoms that overlap with ALS, including muscle weakness, gait disturbance, fatigue, pain, sensory complaints, and impaired balance. Although Lyme disease does not typically present exactly like ALS, it is often included in the differential diagnosis when patients have compatible symptoms together with possible tick exposure.

This distinction is important because Lyme disease is generally treatable, whereas ALS is a progressive neurodegenerative disorder.

Can Bartonella cause neurological symptoms?

Bartonella neurological symptoms may include headaches, neuropathic pain, cognitive difficulties, balance problems, blurred vision, sleep disturbances, and other neurological complaints. The pattern varies considerably from one patient to another.

Because routine laboratory testing may be negative in some patients, diagnosis can be challenging. In selected situations, clinicians may consider specialized testing together with the patient’s history, symptoms, and exposure risk.

When neurological symptoms continue to worsen despite negative routine testing, clinicians may broaden the evaluation based on the patient’s clinical presentation and exposure history.

Why can Lyme disease and Bartonella be difficult to diagnose?

Both Lyme disease and Bartonella infection may be difficult to diagnose because symptoms often overlap with many other neurological disorders. Patients may initially have nonspecific complaints such as fatigue, pain, dizziness, or cognitive difficulties before more recognizable manifestations develop.

Laboratory testing also has limitations. Test performance depends on the timing of infection, the diagnostic method used, and the organism being evaluated. As a result, physicians generally interpret laboratory findings together with the patient’s history, physical examination, and likelihood of exposure.

Why was the diagnosis delayed?

Several factors contributed to the delayed diagnosis in this case. The initial bite was believed to be a spider bite rather than a tick exposure. Standard testing for Lyme disease and Bartonella was initially negative, and the patient’s symptoms continued to evolve over time. Ultimately, specialized PCR testing identified Bartonella, followed later by evidence of Borrelia burgdorferi, illustrating how complex tick-borne infections can occasionally present.

61-year-old woman initially diagnosed with a spider bite develops progressive neurological symptoms

A 61-year-old woman experienced a painful bite while hiking in Minnesota. Because two puncture marks were present and the bite was painful, it was initially diagnosed as a spider bite.

One day later, a large blue ring developed around the bite, followed by diffuse muscle aches and joint pain.

The woman was treated with doxycycline for two weeks. Although her arthritis improved, it did not completely resolve.

Five months later, her symptoms progressed to include blurry vision, impaired balance, muscle pain, night sweats, and insomnia.

At that point, testing for both Lyme disease and Bartonella was negative.

Because she remained concerned about Lyme disease, she sought additional medical evaluation. She was referred to an infectious disease physician, who reportedly stated that he “did not believe in persistent Lyme disease.” She was subsequently referred to a neurologist for magnetic resonance imaging (MRI).

During this period, her blood was included in a research study evaluating improved PCR diagnostic techniques for Bartonella infections.

The investigational testing identified both Bartonella vinsonii and Bartonella henselae.

Approximately one year after the initial infection, the patient consulted an integrative medicine physician, who prescribed clarithromycin and rifampin based on symptoms consistent with Bartonella infection.

Despite treatment, her neurological symptoms continued to worsen.

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Her neurological symptoms continued to progress, and she was referred to a physical therapist, who recommended a wheeled walker because of worsening mobility. Her primary care physician considered whether she might have amyotrophic lateral sclerosis (ALS) or multiple sclerosis (MS).

She also reported that her hips “sounded like popcorn” whenever she walked or climbed stairs.

Hip radiographs demonstrated severe cartilage loss with bilateral hip degeneration, ultimately requiring hip replacement surgery.

Before surgery, the patient underwent another round of testing for Bartonella. Once again, specialized testing confirmed the presence of Bartonella.

In addition, examination of a buffy coat smear revealed “a spirochete-like organism.”

“Given her symptomology and the known possibility of co-infections in Lyme disease, the spirochete was suspicious for Borrelia burgdorferi.”

Subsequent testing confirmed Lyme disease.

Once treatment directed at Lyme disease was started, the patient’s condition improved clinically.

However, the authors noted that “despite the intermittent use of antibiotics for five years, the patient remains positive for Bartonella henselae and Borrelia burgdorferi.”

Whenever antibiotic therapy was discontinued, her symptoms reportedly recurred within approximately three months.

Authors’ Conclusions

  • “This case report illustrates the inadequacy of conventional tests in diagnosing Bartonella spp. infections, and the potential promise of enhanced techniques.”
  • Although serologic testing is commonly used to diagnose both Bartonella and Borrelia infections, this patient repeatedly tested negative by standard antibody testing while specialized FISH and PCR methods were positive.
  • “The limitations of serology for detecting an active infection need to be more clearly understood by the medical community.”

Frequently Asked Questions

Can Lyme disease mimic ALS?

Yes. Neurologic Lyme disease may occasionally resemble ALS because both conditions can involve progressive weakness, gait abnormalities, fatigue, muscle pain, and balance problems. Lyme disease should be considered when the history, exposure risk, and accompanying symptoms are compatible with tick-borne illness.

Can Bartonella cause neurological symptoms?

Yes. Bartonella neurological symptoms may include neuropathic pain, headaches, cognitive impairment, blurred vision, balance problems, sleep disturbances, and weakness. Symptoms vary considerably among patients.

Can Lyme disease and Bartonella occur together?

Yes. Co-infections have been reported in patients exposed to ticks carrying multiple pathogens. When present, co-infections may complicate both diagnosis and treatment.

Why can Lyme disease and Bartonella be difficult to diagnose?

Diagnosis depends on the timing of infection, the laboratory method used, and the patient’s clinical presentation. Negative laboratory tests do not always exclude infection, so clinicians generally interpret test results together with the patient’s symptoms, physical examination, and exposure history.

Can Bartonella mimic multiple sclerosis?

Some patients with Bartonella infection develop neurological symptoms that overlap with multiple sclerosis, including balance problems, weakness, sensory complaints, and visual disturbances. These findings are not specific to Bartonella, and a comprehensive neurological evaluation is necessary before establishing a diagnosis.

Clinical Takeaway

This case report illustrates how Lyme disease and Bartonella infection may occasionally resemble progressive neurological disorders such as ALS or multiple sclerosis. Although this represents a single patient and should not be generalized to everyone with neurological symptoms, it underscores the importance of maintaining a broad differential diagnosis when exposure history, systemic symptoms, or an atypical clinical course raises suspicion for a treatable infectious condition.

When evaluating diseases that mimic ALS, clinicians should consider Lyme disease, Bartonella infection, and other potentially treatable neurological disorders alongside more common neurodegenerative diseases.

Related Articles

Continue learning about Lyme disease, Bartonella, and neurological complications:

Bartonella: symptoms, diagnosis, and treatment
Neurologic Lyme disease: symptoms and diagnosis
Why Lyme disease is frequently misdiagnosed
Lyme disease symptoms: a clinical guide
Persistent Lyme disease: understanding ongoing symptoms

References

  1. Ericson ME, Mozayeni BR, Radovsky L, Bemis LT. Bartonella- and Borrelia-Related Disease Presenting as a Neurological Condition Revealing the Need for Better Diagnostics. Microorganisms. 2024;12(1):209.

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Dr. Daniel Cameron, MD, MPH
Lyme disease clinician with over 30 years of experience and past president of ILADS.

SymptomsTestingCoinfectionsRecoveryPediatricPrevention

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18 thoughts on “ALS and MS suspected in woman later diagnosed with Bartonella and Lyme disease”

  1. This sounds so much like my continuing to find help, thinking I had MS or some terrible disease. I finally found a dr who tested me to find I too had bartonella and Lyme disease. I’ve been on antibiotics off and on now for 5 years and if I get off it recurs.

    1. Not to make things even more difficult but there is a Canadian Herbalist on You Tube that was diagnosed with Lyme.No matter what he did to cure it, it wasn’t budging until he discovered that 1. he is a Targeted Individual & 2. it is Nano form all of the Could seeding or Chemtrails our Governments are doing to us all so Lyme may actually be AI in nano form. My hubby made me one of his devices & it is more powerful that I ever expected. I was dxd with MS supposedly 18+ years ago, have Bulls eye rashes but decided to try this anti nano thing cuz it is less invasive than anything MDs want to do. Just wanted to inform you of this possibility when the antibiotics don’t heal you. Good luck. Here is the Canadian herbalist – https://www.youtube.com/@HerbsPlusBeadWorks

  2. In the UK people are routinely given a diagnosis that describes some of their symptoms, for example MS, ME, or Fibromyalgia, or told (particularly if they are female) that they are imagining the symptoms, or the symptoms are caused by an inability to manage stress, and no further investigations take place. Occasionally some form of “Lyme” test is used, but other TBDs are not considered. Results from blood tests originating from outside the NHS are dismissed, and negative “Lyme” tests from within the NHS are viewed as conclusive. I suspect there are thousands of people here with untreated TBDs and inaccurate diagnoses.

    1. Dr. Daniel Cameron
      Carolyn Glassford Ames

      Exactly the same in Canada. Good point about being female results in more gaslighting than males. It’s like the medical community is stuck in Victorian times, despite the excellent improvement in the representation of women in MDs present in the system. Reliable testing is urgently needed, along with improved education of MDs in tick borne diseases

        1. Dr. Daniel Cameron
          Dr. Daniel Cameron

          There are Lyme disease patients who fail treatment. There are patients who overlook an evaluation for a persistent infection.

  3. Ah, another example of the usual clown show. “He ‘did not believe in persistent Lyme disease.'” Because science is, after all, a type of religion wherein facts are fluid and solely and completely a function of one’s beliefs, right? … right? I hope the patient takes action against this physician-priest. When is this going to change? How many more of us are going to suffer endlessly while attitudes like this are allowed to prevail? Presumably wide-ranging change will not happen until it stings dismissive individual physicians financially on a regular basis, I guess. At this point, I can’t help but think of Plank’s principle (paraphrased): “Science progresses one funeral at a time”.

    https://en.wikipedia.org/wiki/Planck%27s_principle

    At least this patient appears to be in the care of competent physicians at this point. Good for her. I wish her well.

    1. It’s amazing that doctors believe in chronic syphilis but deny the existence of chronic Lyme (Borrelia). The bacteria that causes syphillis and the bacteria that causes Lyme are both spirochetes. (Go figure.)

      1. I agree but Lyme is not a single disease. We named the disease Lyme after our was discovered in Lyme. Original name was Scrapie a disease of Scottish sheep.

        Howland Grace

  4. If more physicians were educated about tick borne illnesses, we might have less chronic lyme, babesia and bartonella cases. Many physicians lack knowledge in this area or refuse to believe what it can do to people.
    There is a great divide among Physicians about tick borne illnesses.

  5. After seeing research that show the cyst form of Lyme would die, after not reproducing, in a lab situation after 3 years I decided to test the theory on myself. For Lyme, I took herbal antibiotics; Cat’s claw and Otoba bark plus resveratrol (and other supporting herbs) NON STOP for 4 years before my symptoms totally subsided. At the same time I took Sida acuta and Houytonia NON STOP for Bartonella. I stopped that protocol after about 3 years because the bart symptoms had subsided and I was becoming allergic to the houytonia (runny nose). I had no symptoms of either for over two years but was bitten again a few times during that time. With every bite I do the CC/Otoba for a week. In the last year I have had a few episodes of mild joint pain for a day or two and I take Cryptolesis for a couple of days. (could be arthritis, muscle, ? but when you are paranoid…) I do need to add that after the first 6 months of no symptoms I slowly progressed into moderately severe ME/CFS (chronic fatigue). After 1.5yrs and finally overcoming that (genetically related to thiamine issue) I proceeded to MCAS (histamine intolerance) which may be related to a just discovered cerebral spinal fluid leak. So which of these came first and how they are all related still hasn’t been determined but ME/CFS was definitely the worse followed by Lyme/Bart/?, CSFL, and MCAS. 8+ years after the misdiagnosis and lack of treatment for Anaplasmosis, I count myself VERY lucky right now! Keep searching for the right answer for you and don’t depend on Drs for help!

    1. I developed MCAS and chronic fatigue after lyme, babesia and rocky mountain spotted fever. I was in top health before lyme.

    2. Hi Allen. Did you tested positive for Anaplasmosis after being sick 8 years ? Which lab did you used ? And which treatment? Does it helped fully ?

  6. Dr. Daniel Cameron
    Dasha Trebichavska, RN, LAc

    The longer the multiple pathogens on the backdrop of struggling immunity go misdiagnosed, the longer one gets to suffer—includes family, friends, plus we get drained emotionally and financially….
    Unless we all start addressing the doctors directly, medical boards, FDA, politicians, we wont see much change.

  7. 4-1/2 years of misdiagnosis, rheumatologists, etc….kept prescribing pain meds, diagnosed with fibromyalgia. I found the right doctor and was diagnosed with FIVE tick-borne diseases, including Bartonella and Lyme. The right doctor can make all the difference.

    1. It is true that most medical doctors are not quite competent regarding vector borne diseases (VBD). Why? Because they do not know, simple as that. They do not have deep knowledge, understanding of the causative pathogens and related symptoms. Sometimes because of their incompetence they are really embarrassed and refuse to say that they do not know the infective pathogens, how to test and treat the nasty intruders. What is the solution? It is simple. Consult competent MDs only and if you have doubts regarding the practitioner, then do not rely solely on their knowledge or reputation. The VBDs are complex infective disorders and not all MDs are competent enough to guide patients on their way to obtaining correct diagnosis, effective treatment plan or potential cure.

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