Featured in: News from CanLyme
Lyme disease documentary makes Oscar’s shortlist
The Academy of Motion Picture Arts and Sciences announced last week that the highly acclaimed Lyme disease documentary, Under Our Skin has made the short list in the category of Best Documentary for the 82nd Academy Awards Oscar presentations in 2010. Continues →-
Lyme documentary: Faces of Lyme – Ambivalence & Controversy
Watch this wonderfully done Canadian documentary on the consequences of poor medical education, Continues → -
This success story cannot happen in Canada without doctors licences being at risk from our very conflict of interest laden health care system that crosses federally to the provinces, then remarkably closely to the United States private organization the Infectious Disease Society of America that is rife with anti-science rhetoric and conflict of interest. Has Canada been the victim of medical fraud? Perhaps.
A family’s fight for their son en route to NCAA tournament history … Continues → -
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 → -
United States: Tick-Borne Disease Working Group 2018 Report to Congress
November 14th, 2018 “A comprehensive understanding of the full economic and societal Continues →
Recent in: News from CanLyme
Time for Canada to follow U.S. recognition of mother-to-fetus Lyme disease transmission, says Mount Allison biologist
Andrew Rankin (arankin@herald.ca) February 11, 2020 SACKVILLE, N.B. — The federal U.S. public health agency has set an example for Canada to follow by acknowledging that Lyme disease could be passed from mother to fetus with serious consequences, says a Mount Allison University expert. “The first step is acknowledging that the transmission happens,” said Vett Lloyd, a biologist and founding Continues →
Nova Scotia, Canada: Lyme disease conference held in Bridgewater
November 17th, 2019 CTV reporter Heidi Petracek @HeidipCTV As the number of reported cases of Lyme disease on Nova Scotia’s South Shore continues to rise, so too does public concern. That’s why hundreds of residents and medical professionals gathered in Bridgewater this weekend for the Bridgewater Lyme Disease Conference. “When you look at the map of infected areas, this province Continues →
1990 archive, MacLean’s magazine: A growing menace
[CanLyme Note: Here we are 30 years later since the formation of the Lyme Borreliosis Society of BC, later rolled into CanLyme, and our government funded agencies with their bureaucrats collude with private medical associations (IDSA, AMMI, CPS), pharma, and medical insurers to deny access to appropriate diagnosis and care to hundreds of thousands. Our elected officials in Canada still Continues →
Lyme disease is an emergency. Instead of feeding the hype, we must support the science.
The controversy may be low-hanging fruit, but what we really need to focus on is a motherlode of hopeful research shining new light on the disease. Oct. 7, 2019, 2:18 AM PDT By Pamela Weintraub, health and psychology editor, Aeon The fight over Lyme disease is one of the hottest topics in medicine right now. Is Lyme underdiagnosed or overdiagnosed? Easily detected Continues →
Illinois expands insurance coverage for those with tick-borne diseases and children requiring EpiPens
[CanLyme Note: Yet another U.S. state ignores the baseless dogma of the private group the Infectious Disease Society of America (IDSA), that chronic treatable active infection does not exist after 3 weeks of antibiotics. Chronic treatable active infection does exist, is devastating, and requires long-term antibiotics just as many diseases do. The Public Health Agency of Canada (PHAC) blindly follows the Continues →
Global TV News: Why Lyme disease is on the rise, explained
[CanLyme Note: Both AIDS and Lyme disease arose as an issue in the late 1970’s with the first case of Lyme reported in Quebec in 1977. As pointed out in this piece, since then there have been over 11,000 clinical trials for AIDS yet only 60 for Lyme disease. Lyme disease research funding in Canada is abysmal and is directed Continues →
‘Scary World’ of Generic Drug Manufacturing, Revealed
[CanLyme Note: This is very important for those being treated for Lyme disease who may not be responding to the treatment. It may be bad medication. Talk to your doctor and pharmacist to possibly switch manufacturers. One wonders what Health Canada is doing about this serious problem.] Ellie Kincaid June 06, 2019 In 2008, investigative journalist Katherine Eban started digging into the generic Continues →
Toronto Sun: Ticks: A ticking Lyme bomb
May 26th, 2019 Nice weather is here and you’re out and about? Be on the lookout for eight-legged menaces on the march. Tick populations armed with the Borrelia bacteria are increasingly creeping into Canada, expanding and growing – and so too the number of tick-borne diseases, predominantly Lyme. It’s a ticking Lyme bomb, and vastly under-detected across Canada. Dr. Vett Continues →
Latest research shows Canada’s decision to fund only one large national Lyme research conglomerate goes against creation of new ideas.
[CanLyme Note: Even worse is that the 4 million tax payer dollars given to the conglomerate, Canadian Lyme Disease Research Network (CLyDRN), is now controlled by members of the anti-science/ethics private group the Association of Medical Microbiology and Infectious Disease of Canada (AMMI) which is the puppet arm of the highly controversial Infectious Disease Society of America (IDSA). Most of the Continues →
Lyme advocates say Canada offers “toxic tokenism” to patients
The Canadian government recently announced new investment in Lyme disease research. However, Canadian Lyme advocates fear that the patient voice will be excluded from the decision-making process. In the following article, the Canadian Lyme Consortium (CLC)–made up of advocates, patients, researchers and practitioners–offers background and context. By Vett Lloyd, PhD; Liz Zubek, MD, CCFP FCFP; Sue Faber and Jennifer Kravis, co-founders, LymeHope; Janet Sperling, CanLyme; Linda Kelso, 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 →
Toronto Star: Everything about Lyme disease is steeped in controversy. Now some doctors are too afraid to treat patients
[CanLyme Note: In the below article there are outrageous, disgraceful, and dangerous comments by Tara Moriarty and Todd Hatchette. Tara says a study showed labs returning 60% false positive test results which is simply not true, or in other words, a blatant lie. That study was not powered to determine true positive or negative results. The conclusion of that study was, Continues →
Papineau Case Against Doctors Delayed an Unreasonable Three Years – A new Charter of Rights Case Perhaps?
Nov 22, 2018 Papineau case delayed 3 years!! The delays in the Papineau case against his physicians may end up being a Charter of Rights case. Legislation has been introduced focused on the criminal justice system but the civil justice system does not seem to be given the same priority. This leaves those with legitimate claims against people or Continues →
United States Annual Cases of Lyme Disease for 2017 Over 400,000
[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 →
Mount Allison University’s Lyme Research Network presents their 2017 – 2018 report on research funded by the Canadian Lyme Disease Foundation
Another successful year building capacity and knowledge within the Canadian science community. These funded students will be our near-future experts. “Overview On May 2017, Mount Allison University announced the formation of the Mount Allison Lyme Research Network, formed with support of the Canadian Lyme Disease Foundation. This network consists of 14 researchers united to provide a comprehensive approach to Lyme Continues →