https://canlyme.com/2018/11/12/canadian-frank-papineau-sues-physicians-dr-pablo-romero-sierra-dr-johnny-brisebois-and-kemptville-district-hospital-in-ontario-superior-court-trial-to-start-november-26th-2018/

Canadian Frank Papineau sues physicians Dr. Pablo Romero-Sierra, Dr. Johnny Brisebois in Ontario Superior court. Trial to start November 26th, 2018

Nov. 12, 2018

Ontario, Canada resident Frank Papineau has had enough and is seeking redress from the courts alleging negligence against two physicians.

In the linked Statement of Claim it is stated that there was also a the claim against Kemptville District Hospital but the claim against the hospital was discontinued in early 2014.

The trial begins November 26th, 2018 and is slated to last 4 weeks indicating just how seriously this case is being taken.

Other Canadians with Lyme disease, their families, physicians, patient advocacy groups, and others not only in Canada but around the world will will be following this case with great interest to see if the courts can begin to offer protections for the abuse of thousands of patients by the current health care systems that have failed them so miserably.

Making this more significant is that it is taking place in Canada’s capital city, Ottawa, Ontario, under the nose of the federal Public Health Agency of Canada, and federal legislators that to date have done little to bring ethical treatment of Lyme disease patients to the offices and hospitals of Canada.  Also situated in Ottawa is the multi-billion dollar Canadian Medical Protective Association (CMPA), a non-for-profit deep-pocketed fund that physicians have access to for the legal woes and costs.

This is truly a David against Goliath case where the physicians have this access to mega-millions of dollars for their defence, as opposed to any individual.

One has to wonder where the CMPA was while almost 100% of Canadian physicians, who appropriately diagnosed and treated Lyme patients clinically, were forced out of business or forced to stop treating Lyme patients simply because they chose to not follow very-restrictive opinion based (not science-based) guidelines imposed upon Canadian doctors via the Association of Medical Microbiology and Infectious Diseases of Canada (AMMI).

Previously an Ontario physician was sanctioned by the College of Physicians and Surgeons of Ontario for not following the terrible Infectious Disease Society of America guidelines imposed by AMMI.  He appealed the decision to the Ontario Health Professionals Appeal and Review Board who sided with the doctor stating he did not have to follow those [dangerous] guidelines …

“The Board also finds that the Committee reached an unreasonable decision when it decided to caution the Applicant for failing to document the rationale for not following the recommended guidelines for treatment of Lyme disease. The Board notes that the Applicant’s consultation letter to the patient’s family physician, dated December 10, 2010, contained a detailed explanation for the treatment recommended by the Applicant.”

It is hoped that the court-room for the Papineau case will be filled with patients and patient advocates.

You can read the now-public Frank Papineau Statement of Claim here.

Of interest is also the report submitted by representatives of many countries including Canada to the United Nations Human Rights Commission in June 20

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More on legal cases regarding Lyme/MSIDS:  https://madisonarealymesupportgroup.com/2018/10/03/aussie-widow-of-lyme-disease-victim-to-sue-nsw-health/

https://madisonarealymesupportgroup.com/2017/11/15/lyme-patients-file-lawsuit-against-idsa-and-insurers-over-treatment-denials/

This is the inevitable outcome of ignoring and mistreating people for decades. This is not the only lawsuit brewing and I predict much more to come. People in Lyme-land are frustrated, suffering, and fed up.

https://madisonarealymesupportgroup.com/2017/09/25/speaking-of-fake-science-fifty-seven-million-anti-trust-lawsuit-against-cdc-lyme-tests/ An unprecedented anti-trust law suit of $57 million is being prepared against the CDC. They are accused of deliberately suppressing the use of an accurate DNA direct diagnostics for Lyme disease.

https://madisonarealymesupportgroup.com/2017/10/13/1st-officially-recognized-report-on-violations-of-lyme-patients-human-rights-is-released-updating-borreliosis-diagnostic-codes/ Human rights violation has been reported to the U.N. regarding the treatment of Lyme patients. https://madisonarealymesupportgroup.com/2017/11/14/thayer-interview-commentary-on-tick-borne-disease-working-group/

https://madisonarealymesupportgroup.com/2017/10/06/remembering-dr-masters-the-rebel-for-lyme-patients-who-took-on-the-cdc-single-handedly/  This story should be made into a movie.  For real.  Way back in 2003 Weintraub interviewed Dr. Masters of Cape Girardeau, Missouri, about Lyme disease in the South, though the “powers that be,” continued to deny it (and still do).

The CDC shenanigans are completely outrageous and we must never forget what they have done through the years to very ill patients.