BITTEN: Canadians fight for Lyme disease diagnosis and treatment

Video focusing on the lives of Canadians for a change. Although there is a focus on the story of a young woman from North Bay (named Nikki) the stories of Justin Beeber, Avril Lavigne and Justin Woods (who runs a private Lyme research lab in Pefferlaw, Ontario) are discussed to an extent as well. All discuss the diseases’ ability to morph into other apparent diseases (like Lupus) and the great length of time it took for all to be properly diagnosed. Medical tests (like ALyva Test) look for certain antibodies which are created by the bacterium “Borrelia burgdorferi” but often those antibodies take days for the body to create, so the initial blood tests come back “Negative for Lyme disease”.

If patients are tested too late after a bite, the bacterium can morph into another apparent disease. In addition, less than 30% of patients have the classic, initial “Bullseye Rash”. Because Canadian doctors are legitimately afraid of losing their medical licences, due to stricter regulations in Canada, they tend to lean towards “evidence based science” to protect themselves rather than taking chances with antibiotics and treatment such as doctors do in the USA. Testing is also more sophisticated in the USA. Many patients go to the USA, especially Florida to be properly diagnosed for Lyme disease. A fascinating video.

Massachusetts doctor develops preventative shot for Lyme disease

Dr. Mark Klempner, a professor of medicine at the University of Massachusetts, has developed a drug that may prevent Lyme disease from infecting humans. The drug, known as Lyme PrEP, was approved for its first human clinical trial by the Food and Drug Administration (FDA) at the end of 2020.” However, this older article concludes by saying:

“Assuming the tests go as planned, it’s predicted that Lyme PrEP could be available by 2023.”

There appears to be no further discussions as to the current status of the drug/vaccine.

Read Full Article Here >

The Quiet Epidemic

Many Lyme disease patients suffer for a long time before receiving a diagnosis. Their symptoms, including pain and paralysis, often seem to indicate other diseases, like MS. The fact that they have been bitten by a tick that carried Lyme disease often only emerges after many examinations. This is exactly what happened to two of the film’s subjects: a girl from Brooklyn, NY and a researcher at Duke University. Both decided to take matters into their own hands and began carrying out independent research into their symptoms. Both ended up in the middle of a controversial medical debate and found themselves having to fight hard for adequate treatment.

Understanding the Persistent Symptoms in Lyme disease

Although initially discovered in 1975 in the Town of Lyme, Connecticut, it took the medical profession almost 45 years to accept the fact that the disease could cause long term effects because the initial symptoms of fever, pain and swollen joints could disappear after a while only to come back again later…but disguised as another disease, often as: Dementia, Chronic Fatigue Syndrome, Lupus, Alsymers, Fibromyalgia, ALS, Rheumatoid Arthritis and especially as Multiple
Sclerosis. It took years before they recognized Lymes disease as being “The Great Imitator” (just like Syphilis).

There is a good description of the bacterium “Borrelia burgdorferi”…appearing to look like a cork screw (or spirokete) which can penetrate deep into the cartilage of knee and hip joints or into heart muscles. It can migrate to and infect any organ of the body, including the brain and can cause psychological problems like OCD (Obsessive Compulsive Disorder). The history of the scandals in the USA pharmaceutical industry was examined at length and demonstrates how power, money and greed contributed to the scientific and medical community becoming biased towards certain views, delaying the realization of the truth about this disease.

A fascinating, must see video full of depth and knowledge.

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