Category Archives: Lyme in New Brunswick

Recent in: Lyme in New Brunswick

Canadian MP Len Webber addresses Minister of Health on Lyme disease

Minister of Health Patty Hajdu readily admits there is “still lots to learn” about treatment of Lyme disease but as typical opts to keep sick people sick without options of extended antibiotic treatment that has helped hundreds of thousands of people who had to leave Canada for help. Instead she wants more research, none of which is going to help Continues →

Canada loses a great Lyme disease defender, Paul Haefling author of Oh Canada: The “Politicks” of Lyme Disease

Obituary Haefling, Paul M.A. (English), LL.B – Passed away surrounded by his loving wife Catherine of 54 years and family members at the Wellington Terrace Nursing Home in Fergus on Monday, January 13, 2020. Paul Haefling, in his 79th year, was the husband of Catherine (Lipton) Haefling. Predeceased by his parents Jerome and Irene (Sullivan) Haefling and by his sister Continues →

Canada: Serious flaws in a medical system lacking medical and scientific ethic

Presenting at a Lyme disease conference held in Bridgewater, NS, in November 2019, it was said that Nova Scotia lacks proper protocols when dealing with the ignored epidemic of Lyme and tick-borne diseases [TBD’s]. We have the highest incidence in Canada conservatively estimated as 454/ 100,000 across the province to as high as 1,826/100,000 in the western zone. These estimates Continues →

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 →

Talking Ticks and Lyme Disease Testing with Dr. Vett Lloyd

Most researchers are inspired to specialize in a particular field by a fascinating graduate course, an inspiring professor or a promising lab test. Dr. Vett Lloyd has a slightly more unique reason for devoting a large portion of her career to the study of Lyme disease: she was actually diagnosed with it. A geneticist by training, with an MSc-equivalent degree Continues →

Parenting When Children Have Lyme Disease: Fear, Frustration, Advocacy

Emilie M. Gaudet 1 , Odette N. Gould 1,*, Vett Lloyd 2 1 Department of Psychology, Mount Allison University, Sackville, NB E4L 1C7 Canada 2 Department of Biology, Mount Allison University, Sackville, NB E4L 1G7 Canada * Author to whom correspondence should be addressed. Healthcare 2019, 7(3), 95; doi.org/10.3390/healthcare7030095 Abstract Increasing numbers of Canadians, including children and adolescents, are being infected with Borrelia burgdorferi and contracting Lyme disease. 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 →

Listen to CanLyme president Jim Wilson on CBC radio – Radio Canada International

August 5th, 2019 [CanLyme Note: This is just one of several interviews given by Jim Wilson the morning of August 5th. Live separate interviews were done for CBC radio Toronto, Quebec City, Winnipeg, Regina, Yellowknife, Whitehorse, Vancouver, and Montreal, each at different time slots.] “We’re in the middle of a Canadian summer, and people are enjoying the best of what Canada’s Continues →

Join Us in New Glasgow, Nova Scotia for Lyme presentation

Jennifer MacLean and Amy Haynes-Desjardins have arranged for a Lyme and other tick-borne disease presentation to be held in New Glasgow, NS on Friday evening, September 6th, 2019 at the Pictou Wellness Centre 2-2756 Westville Rd, New Glasgow, NS – 4:30 to 6:00 PM for Health Care Professionals 7:00 to 9:00 PM for the public Presenters will include; Vett Lloyd, 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 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 →

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 →