Featured in: Featured
Virginia passes law forcing physicians to disclose the limitations of tests
Va. now must disclose the flaws in Lyme disease testing Tuesday, February 26, 2013 BY MARKUS SCHMIDT Richmond Times-Dispatch Lyme disease is one of the fastest-growing infectious diseases in the United States, but despite testing, many patients are not aware that they are infected until it is too late. New legislation passed by Virginia’s General Assembly is supposed to change Continues →-
The Ad Hoc Patient and Physician Coalition From Around the World Reject Newly Proposed IDSA Guidelines
The Ad Hoc Patient and Physician Coalition Comments of the IDSA Proposed Lyme Guidelines Continues → -
Response by Nova Scotia’s Chief Medical Officer of Health relative to Lyme disease comes under serious scrutiny as to it’s relevance to ‘true’ science.
[CanLyme Note: Dr. Strang’s response below to CanLyme director Rob Murray’s letter from 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 → -
CTV’s Avis Favaro “Mothers on a mission to prove Lyme disease can be passed to unborn child”
“These mothers and their kids struggled for years with severe dizziness, pain, digestive Continues →
Recent in: Featured
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 persistent hard work in making this review happen and inviting us to participate in their journey. Also, the immensely important assistance and input from Ralph Hawkins, MD, and Vett Lloyd, PhD, brought the science to the forefront. Finally, much needed dialogue can begin on Continues →
United States: Tick-Borne Disease Working Group 2018 Report to Congress
November 14th, 2018 “A comprehensive understanding of the full economic and societal cost remains unknown. It is likely orders of magnitude higher and potentially a $50- to $100-billion-dollar problem for the United States, although more research is needed (Vanderhoof & Vanderhoof-Forschner, 1993; Zhang et al., 2006).” “The U.S. National Institutes of Health (NIH) and CDC spend $77,355 and $20,293, respectively, per new surveillance case of HIV/AIDS, and $36,063 and Continues →
Lyme disease vastly under-detected in Canada, according to new study
Mount A biologist co-authors research that suggests only 3-4% of Lyme cases are officially diagnosed Friday October 20th, 2018 A new study published in the journal Healthcare suggests the vast majority of Canadians who have Lyme disease are slipping through the cracks. The research was done by Vett Lloyd, a Mount Allison University biology professor, and Dr. Ralph Hawkins, a Continues →
Twins Ice Cream Parlour in lovely Port Rowan, Ontario, for years has been very active in raising awareness and funds for Lyme disease.
On the north shores of Lake Erie sits the idyllic community of Port Rowan, Ontario. It is a beautiful community whose residents, businesses, and visitors for three years now have joined together with the very popular Twins Ice Cream Parlour on the Civic holiday weekend to raise awareness about the scourge of Lyme disease and to raise funds for CanLyme Continues →
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 Equity in ICD11 Borreliosis Codes by CanLyme president and founder, Jim Wilson. Presentations were made in June 2018 to the United Nations in Geneva, Switzerland, and a report was submitted to the World Health Organization in March 2017 co-authored by Canadian, Vett Lloyd PhD, with recommendations for changes to Continues →
Canadian Lyme Consortium research network wants you! Such an important cause, please read and pass along.
June 23, 2018 Hi Folks, CanLyme is a proud and active supporter of the Canadian Lyme Consortium research network and here is their most recent communication… ————————————————- Greetings fellow members of the Lyme community; I am reaching out on behalf of the Canadian Lyme Consortium (CLC) research network to the Canadian Lyme community with an important update and invitation. As Continues →
Corruption and Human Rights Violations Against Lyme Doctors, Scientists and Parents Now on United Nations Record
The 2018 Report ‘The Situation of the Human Rights Defenders of Lyme and Relapsing Fever Borreliosis Patients’ was submitted to Special Rapporteur Michel Forst and to Special Rapporteur Dr. Dainius Puras of the United Nations in March 2018. This resulted in a meeting between United Nations Human Rights Council Special Rapporteur Forst and medical professionals, scientists, human rights experts and Continues →
A home for patient-oriented research
[CanLyme Note: On the Lyme disease file in Canada the patient has been rejected, removed, and denied by the same people we pay to protect us. We put forward experts, they are not accepted as experts. We put forward scientific evidence, it is ignored. The Canadian Institute of Health Research and the Public Heath Agency of Canada collude to exclude the Continues →
“She looked like a stroke victim”
[CanLyme Note: How is it that physicians are so under-educated and misinformed on this disease after it being here for so many years? The physician said the symptoms were not classic and were too soon!!! When are our College’s of Physicians and Surgeons, including the provincial and the Royal College going to start acting like responsible, ethical institutions. Time for oversight Continues →
Lawsuit: Insurance companies conspiring with physician members of the Infectious Diseases Society of America
November 19th, 2017 Lynne LaRowe Texackana Gazette Major health insurance companies are accused of putting profits over patients suffering from Lyme disease in a lawsuit filed recently in a Texarkana, Texas, federal court. The suit alleges companies including Blue Cross, Kaiser and Aetna violated RICO and anti-trust laws when conspiring with physician members of the Infectious Diseases Society of America Continues →
Prof. Christian Perronne, MD, PhD, outlines his history and the history of resistance within mainstream medicine regarding Lyme disease.
Christian Perronne, MD, PhD, is Professor of Infectious and Tropical Diseases at the Faculty of Medicine Paris-Ile de France-Ouest, University of Versailles-St Quentin en Yvelines (UVSQ), Paris-Saclay, France. He is chief of a Department of Medicine at the Raymond Poincaré University Hospital in Garches (Hauts-de-Seine), belonging to Assistance Publique – Hôpitaux de Paris, the Greater Paris University Hospitals. My fight Continues →
Unprecedented claim against the CDC over Lyme tests
August 23, 2017 written by Huib In the USA 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. You can read about the aim and potential impact of this lawsuit in this article. “In the current situation, even in Continues →
Listen to today’s testimony of Dr. Ralph Hawkins, Dr. Liz Zubek, Canadian Blood Services and the Public Health Agency of Canada in the standing health committee.
June 8th, 2017 You can listen to the interesting testimony here… Dr. Njoo from the Public Health Agency of Canada believes patients are too stupid to be equal partners in setting guidelines on diagnostics and treatment. Only his buddies at AMMI, IDSA and the US CDC are qualified to have the final say… the same group who have failed us Continues →
New York Times: More Than 80 Percent of Patient Groups Accept Drug Industry Funds, Study Shows
[CanLyme Note: We have been approached by various pharma industry to work with them but we have steadfastly refused in order to maintain our independence, so as to not be beholding to the for-profit industry. Now if government and the Canadian medical associations and societies could shake their relationship with big-pharma then perhaps better health care would result.] March 2nd, 2017 Continues →
Canadian tax payer funded Lyme research not good value for dollar
In December of 2016 a Canadian article was published in PLOS ONE proporting itself as a good systematic review about Lyme disease testing accuracy. CanLyme has been trying to work closely with government on the value of good science as good evidence yet once again the government of Canada has managed to publish low-quality material without any patient expert input into Continues →