Category Archives: Lyme in Nova Scotia

Recent in: Lyme in Nova Scotia

How many cases of Lyme disease are we missing?

June 27th, 2019 DONNA LUGAR I participated in a “Tick Talk” in Bedford with Lisa Ali Learning of AtlanTick on June 25. One takeaway from that meeting, for me anyway, is that we are not doing enough to ensure Nova Scotians are adequately aware of the risks associated with tick bites. One family, new to the country, had never even Continues →

There’s no evidence quick dose of antibiotics will stave off Lyme

[CanLyme Note: Canadians have got to beware of information produced by any members of the Canadian Lyme Disease Research Network (CLyDRN) as their information does not serve you the public, but instead serves the for-profit medical industry and their many components while patients struggle with a lifetime of disability and multiple daily drugs not intended to fix the disease itself. They Continues →

Lyme disease treatment needs better approach, Conservatives say

Tim Houston and the Progressive Conservatives are urging the province to take a new approach to combating the growing Lyme disease endemic in Nova Scotia. “The province’s focus on prevention is skirting the real issue that people will continue to be bitten by ticks in this province and people are continuing to contract Lyme disease,” said the Progressive Conservative leader. Continues →

Lyme disease study raises possibility of mother-to-baby transmission

Andrew Rankin (arankin@herald.ca)  May 15th, 2019 A scientist who co-authored a recent Public Health Agency of Canada study on the impact of Lyme disease during pregnancy says the illness can have fatal consequences for a developing fetus if the mother goes untreated. “Miscarriage, newborn death, and newborns with respiratory problems or jaundice have been found to occur,” said American epidemiologist Alison 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 →

Chronicle Herald: COUNTERPOINT: Hitting the wall of denial with chronic Lyme

[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 →

Nova Scotia’s top doctor takes heat over retweet dismissing chronic Lyme disease

[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 →

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 →

‘Every season is tick season’: Experts warn of winter Lyme disease risk

People have ‘let their guard down’ and aren’t checking for ticks as weather cools, says zoologist   Laurenne Schiller loves taking her dog Cousteau for walks along Halifax trails as the weather cools. But even after the first dusting of snow this week, each walk finishes with a head-to-toe check for blacklegged ticks on her and her collie.   “”They’re Continues →

Halifax: Unconscious Collective Vocal Ensemble (UCVE) to stage two performances to raise funds for CanLyme

Nov 24, 2018 Save the dates!! For a truly unique experience that you will love come and see the Unconscious Collective Vocal Ensemble (UCVE). They will be putting on two performances in the KTS Red Room, University of King’s College in Halifax… 7 PM Friday the 30th of November (18-11-30) 7 PM Saturday December 1st, 2018 (18-12-01) Bring your family and friends!! These performances will Continues →

OPINION: Lyme disease tunnel vision plagues provincial authorities

Nov 3rd, 2018 Chronicle Herald newspaper Halifax, Nova Scotia, Canada by Jane Bailey. Re: “Nova Scotia’s health system has a handle on Lyme” (Sept. 18 opinion piece by Dr. Robert Strang). I was appalled at the inaccuracy and inadequacy of the information that he is supplying to Nova Scotians — patients and doctors — about Lyme disease. A 2012 Health Continues →