I know for example: there was a guy who got bitten by a tick in Australia and yet doctors still think “nothing is wrong” just because Australia doesn’t recognize Lyme Disease since their argument is “no scientific proof that ticks in our country transmit the bacteria” which sounds stupid when there are cases of people having Lyme Disease there.

And he’s not the only one: as a woman shared the symptoms he had, but Australia FOR SOME reason is still in denial as their counterargument sticks on “NO SCIENTIFIC PROOF THAT OUR TICKS HAVE IT” so she spent money on getting the results in another country where Lyme Disease is officially recognized paid from her own pocket.

In comparison:

  • is Lyme Disease recognized in the United States?
  • If so, how common is it amongst the population?
  • Otter@lemmy.ca
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    14 hours ago

    So they don’t explicitly mention “chronic” Lyme disease in the video, and I couldn’t find any other articles from looking up the names mentioned, but it does sound like that’s what is being talked about here.

    What I would be curious about is if these patients got the antibody test. If they didn’t, that seems like a relatively easy policy fix. Bacteria can spread to other countries and go undetected, and the test isn’t that invasive compared to the peace of mind it would give patients. Same

    However if they did get the test and it came back negative, then it gets more complicated. Doctors don’t want to put someone on treatment for something that can’t be detected. Every medication has side effects and you would end up harming someone without evidence of a benefit. Where it gets messy is when people go for “diagnosis” or “treatment” abroad.

    I did actually find this from last October

    https://www.health.gov.au/sites/default/files/2025-11/australian-government-response-to-the-senate-community-affairs-references-committee-report-access-to-diagnosis-and-treatment-for-tick-borne-diseases.pdf

     Overview
    
    The Australian Government appreciates the opportunity to respond to the Senate
    Community Affairs References Committee list of recommendations on the Access to
    diagnosis and treatment for people in Australia with tick-borne diseases. The Government
    thanks the Committee and the various stakeholders for their valuable and thoughtful input
    to the Inquiry.
    The Government acknowledges the concerns of patients who are facing issues accessing
    diagnosis and treatment with tick-borne illnesses. In early 2013, the Department of Health,
    Disability and Ageing began engaging with patients, medical practitioners, and advocacy
    groups to discuss concerns about Lyme disease. In 2016, the department engaged and
    addressed the Senate Inquiry recommendations into Growing evidence of an emerging tick-
    borne disease that causes a Lyme-like illness (2016 Inquiry) through a range of measures
    such as public education materials, research and guidance for medical practitioners. As a
    result, the department has gained a deeper appreciation and growing concern for those
    Australians experiencing issues relating to tick-borne diseases.
    This response addresses the specific recommendations raised in the current Senate
    Committee's Report. The Government remains open-minded about the cause of the various
    complexes which manifest as a range of chronic debilitating symptoms. The best outcome
    for patients and health practitioners is to not draw conclusions based on poor levels of
    evidence, but to consider each patient thoroughly in a multidisciplinary medical approach
    that makes the best use of clinical expertise and available diagnostic skills and technology.
    The Government remains engaged with the patient and medical community to continue to
    find, share and understand the evidence associated with tick-borne diseases. The
    Government hopes its continued work with clinical medicine and research communities will
    result in answers and relief for patients and their families