Featured in: Government
Canada: A systematic review on the impact of gestational Lyme disease in humans on the fetus and newborn[CanLyme Note: We at CanLyme want to thank Sue Faber and Jennifer Kravis for their excellent Continues →
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Ground Breaking Recognition of Lyme Borreliosis in 11th International Classification of Diseases – World Health Organization[CanLyme Note: CanLyme was represented on the international Ad Hoc Committee for Health Continues →
Corruption and Human Rights Violations Against Lyme Doctors, Scientists and Parents Now on United Nations RecordThe 2018 Report ‘The Situation of the Human Rights Defenders of Lyme and Relapsing Fever Continues →
Recent in: Government
Advocates claim policy harms patients and violates HHS standards for information quality Washington, DC – WEBWIRE – Tuesday, February 19, 2019 Advocates for Lyme disease patients are calling on the Centers for Disease Control and Prevention (CDC) to withdraw its endorsement of single-dose antibiotic prophylaxis for prevention of Lyme disease after a tick bite. A key limitation of the recommendation Continues →
[CanLyme Note: Robert Strang has been purveyor of misinformation relative to Lyme disease; it’s prevalence, the chronic nature of the disease, and the ability of the bacteria to survive short term antibiotics, for so long and with such an anti-science, pro-opinion bias see that he is disqualified to represent public health, yet the Nova Scotia government has done nothing to protect it’s Continues →
Chronicle Herald: Chief medical officer’s Lyme disease retweet likely violated policy — legal expert
January 29th, 2019 by Andrew Rankin The Chronicle Herald HALIFAX, N.S. — A recent tweet by Nova Scotia’s top doctor dismissing chronic Lyme disease as a pseudoscience supported by a cult following appears to violate the province’s social media policy, says a Dalhousie University law professor. “What I also don’t understand is what does he really mean by the retweet,” said Continues →
[CanLyme Note: Once you read this article you will see that the Nova Scotia Minister of Health chimed in with the usual pre-formatted line that the province follows evidence-based guidelines. For research and science to become evidence, it requires transparent debate with stakeholders. There is no more important stakeholder in health care than the sick patient and their experts. No such Continues →
Canadian government asked by international Health Equity committee to reverse secretive, harmful, and unethical interference that will affect mothers and children worldwide.
December 22, 2018 Dear Prime Minister Trudeau, Honorable Minister Ginette Petitpas-Taylor, Honorable Minister Jody Wilson-Rebould, Dr. Mithani, Dr. Tam, Honorable Andrew Scheer, Elizabeth May and Jagmeet Singh and Kimberly Elmslie, I am the Director of the Ad Hoc Committee for Health Equity in ICD11 Borreliosis Codes (or Ad Hoc Committee). The Ad Hoc Committee is fully voluntary international group including Continues →
BREAKING NEWS: The Public Health Agency of Canada Secretly Implements Global Act Against Children with Congenital Lyme
[CanLyme Note: As a result of the allegations revealed in the below article by Jenna Luche-Thayer, CanLyme wrote the following letter to Canadian leaders, sent December 21st, 2018, “Dear Prime Minister Trudeau, Honorable Minister Ginette Petitpas-Taylor, Honorable Minister Jody Wilson-Rebould, Dr. Mithani, Dr. Tam, Honorable Andrew Scheer, Elizabeth May and Jagmeet Singh, The news that we have received from within the Continues →
[CanLyme Note: The numbers reflected by the CDC in no way represent the total number of cases occurring annually in the USA. As per the CDC press release in 2013 they acknowledge that “surveillance data” only gathers about 10% of the true numbers of cases putting a more realistic total annual count for 2017 at over 400,000 cases.] ————————————————- In 2017, Continues →
The Situation of Human Rights Defenders of Lyme and Relapsing Fever Borreliosis Patients: Edition One March 6, 2018
Thanks to the tremendous effort of Jenna Luché-Thayer the report was presented at the United Nations in Geneva, Switzerland, in June 2018 by several of us on the The Ad Hoc Committee for Health Equity in ICD11 Borreliosis Codes representing many different countries affected by poor policy. Authors: Jenna Luché-Thayer, Holly Ahern, Robert Bransfield, Joseph Burrascano, Anne Fierlafijn, Theresa Denham, Huib Kraaijeveld, Continues →
June 3, 2018 Chronicle Herald – Public health failing to address Lyme disease crisis, says author From the article titled “Public Health failing to address Lyme disease crisis says author” this is a quote … “Heather Fairbairn, a spokeswoman with the province’s public health department, issued a statement to the Herald last week saying in part, that Lyme disease and other Continues →
[CanLyme Note: We have had many meetings with the BC CDC over the years pointing out the problems with their testing but were completely ignored. Even this more sensitive test will miss many cases. Meanwhile mothers were being accused of having Munchausen by proxy syndrome by doctors at the BC Children’s Hospital simply because they were not accepting the infectious disease Continues →
[CanLyme Note: The Lyme disease disaster for Canadians is an excellent example of how the ‘self-regulating’ medical colleges and medical associations have woven themselves into the publicly funded health care system positioning themselves as the only experts, and policing any physicians who disagree with them, out of business. No outside scientific expertise is allowed no matter how much harm is done Continues →
Tuesday, April 10, 2018 [CanLyme Note: The Canadian system via the Pubic Health Agency of Canada (PHAC) and the Canadian Institute of Health Research (CIHR) adopted the same corrupted, biased position of the US CDC. Now we need Canadian parliamentarians to do the right thing for the sick. Last year, Health Canada announced there would be a tiny bit of Continues →
CanLyme has questioned the self-policing of physicians for years as it protects bad nonsense – NOW CHANGE MAY HAPPEN? Are our politicians listening?
[CanLyme Note: This is not isolated to Ontario, it is Canada and world-wide. Many provinces and countries have given the right to medical colleges and associations to self-police. The process has been corrupted and abused for years with many doctors given far too light consequences while on the other hand they use self-policing to force doctors to follow bad policy Continues →
Lyme disease in Ireland: This is a global threat that is being denied by government bureaucrats around the world who are tied to the United States Center for Disease Control.
Article on Lyme disease sparks calls for awareness campaign March 11, 2018 A UK SCIENTIST, whose daughter contracted Lyme disease in Bantry, says she would like to be part of an Irish awareness campaign on the tick-borne disease. Responding to reports of high rates of the disease in West Cork and South Kerry, detailed recently in The Southern Star, Helga Frost Continues →
The Canadian Lyme Consortium, representing scientists, clinicians and patients provides an update regarding government promised research grants.
March 9th, 2018 The Canadian Lyme Consortium, representing a united and transparent relationship between patients, clinicians and researchers has issued an update detailing the situation with the Canadian Institute of Health Research (CIHR) granting process. Ethics and good science do not seem to be relevant at CIHR as Health Canada continues to fail Canadians. Read full update