chronic-lyme-disease

Chronic Lyme disease patients dismissed by medical community

In their article, “Medical Gaslighting and Lyme Disease: The Patient Experience,” Fagen and colleagues examine the extensive range of gaslighting techniques experienced by chronic Lyme disease patients.¹ And, explore the demographic variables (i.e., geographic location) that may be associated with higher rates of medical gaslighting.

What is medical gaslighting? Gaslighting refers to a type of manipulation which results in a person questioning their own reality or experiences. Medical gaslighting occurs when a medical professional dismisses or downplays a patient’s symptoms.

ONLINE SURVEY: Chronic Lyme disease patients

The authors conducted an online survey involving nearly 1,000 individuals who had Lyme disease or had a child with Lyme disease. The majority resided in the United States (48%), Australia (15%), Canada (15%), Ireland (9%), and the UK (8%).

“The number of Lyme disease patients with lingering symptoms in the US was projected to be as high as 1,944,189 in 2020.”

Respondents answered questions about their experiences with the medical community while they were in the process of being diagnosed and treated for Lyme disease. The majority (71%) had received a diagnosis based on a positive blood test ordered by a physician, while 13% were diagnosed based on a physician’s symptom-driven clinical diagnosis.

STUDY RESULTS:

  • The authors found that patients were “much more likely to be told by practitioners that they were just overreacting to their symptoms, there was no such thing as [chronic Lyme disease], or that their symptoms were caused by normal aging, mental illness or stress.”
  • “Many patients also felt that medical professionals frequently implied the patient’s symptoms were merely psychosomatic.”
  • “… a patient’s positive blood test status did not influence how likely a doctor was to believe the patient had Lyme disease.”
  • “physicians in Lyme endemic regions were more likely to grant a patient’s request for a Lyme disease test than those in non-endemic regions.”

Doctors frequently did not believe a patient had Lyme disease, even though they had a positive blood test.

Additionally, patients in non-Lyme endemic states were frequently told:

  • they could not have Lyme disease because there were no ticks or Lyme disease in their area;
  • they did not have Lyme disease despite having a “bulls-eye” rash;
  • their Lyme disease symptoms were just in their head.

According to the study, “a striking majority of respondents felt that they were treated as a marginalized patient group.” They were also told by medical professionals that they were overreacting and that [chronic Lyme disease] does not exist.

“We also contend that a median of 10 doctors seen before diagnosis is, in and of itself, highly suggestive that medical gaslighting occurred,” the authors state. And, of particular concern – physicians dismissed a Lyme disease diagnosis despite having a positive blood test.

The authors point out, “attributing symptoms solely to the aging process, dismissing patients’ bloodwork results, and outward manifestations of a medical condition (e.g., the EM rash) are indicative of medical gaslighting.”

CONTESTED ILLNESSES

The authors point out, “Many diseases were previously thought to be contested illnesses because their biological basis was not understood.” These include inflammatory bowel disease, endometriosis, peptic ulcers, and, more recently, Long COVID.

“The contestation of [chronic Lyme disease] has created a climate in which doctors may be less inclined to believe that Lyme disease patients’ persistent symptoms are attributable to an ongoing infection. Thus, such patients may not receive treatments for their underlying infection,” the authors state.

References:
  1. Fagen, J.L.; Shelton, J.A.; Luché-Thayer, J. Medical Gaslighting and Lyme Disease: The Patient Experience. Healthcare 2024, 12, 78. https://doi.org/10.3390/healthcare12010078

Comments

25 responses to “Chronic Lyme disease patients dismissed by medical community”

  1. Funny, after going on now 15 years two of which I didn’t know I had Lyme though I found the tick and bulls eye rash, I never met the CDC or IDSA criteria. A few months back I tested positive from an ELISA…but having suffered from now carditis, severe neuropathy, vasculitis among a litany of symptoms, I would whole heartedly agree that yes, it is indeed in our heads and beyond those doing the gaslighting, this suffering including children going on 50 years is denial & shameless…and quite scandalous if one knows the history of those people and agencies behind the scenes and those doing the gaslighting.

    1. You are not alone. What a shame.

  2. As we learnt from the beginning being so isolated from the rest of the medical world you have no idea of s we hats happening. So many symptoms presenting but in my wife’s case extreme inflammation and neurological pain pain that nobody could understand. Then came the seizures and lists of trips to emergency or ambulances at our home. As my wife layed on the floor one day and l looked down at all the ambos trying to help my Ten year old daughter looked at me in a frightening look and asked me Is mummy going to die that moment l new l had to step up and knock on many doctors doors to be only made to feel like an alien till we found the labs that could do proper testing because she had no immune system left by this stage and here is where our journey began after fives years of nothing or you have fibromyalgia. Rheumatologist and neurologists are a complete embarrassment to even sit in the same room just totally no understanding of the pathogens that creates borelliosis neurological bartonella babessia EBV
    Cocksackie viruses adreanal melt down autoimmune conditions the list is long but this is e we here l will leave sixteen years forward and Australian model of appropriate testing and treatment doesn’t exist

    1. I have patients who have seizure like activity from Lyme disease with a normal EEG.

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