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 →
Tag Archives: research
Segment 1 LYME AND REASON: THE CAUSE AND CONSEQUENCE OF LYME DISEASE Segment 2 LYME AND REASON: BATTLES AND BREAKTHROUGHS AGAINST LYME Segment 3 LYME & REASON 2.0: LYME DISEASE & THE VOICES OF CHANGE Segment 4 LYME & REASON: THE POWER OF INNOVATION Segment 5 LYME & REASON: DR. KRISTEN HONEY
[CanLyme Note: This for profit money drive takes medical research away from cure to ‘a drug for every symptom’. In Canada, relative to Lyme disease, the private Association of Medical Microbiology and Infectious Disease of Canada (AMMI), is an extension of the ‘do not cure’ medical money machine. They offer opinion and poorly designed research to support the ‘do not treat 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 →
Nov. 1, 2018 A study recently published in Scientific Reports discovered that 65% of Lyme disease patients irrespective of their disease stage respond to several microbes. As a consequence, the authors have demonstrated that microbial infections in individuals suffering from Lyme disease do not follow the “one microbe, one disease” status-quo. Moreover, the probability that Lyme disease patients would respond Continues →
Are you a parent in Canada with a child struggling with Lyme disease? Canadian researchers want to hear from you!!
May 2019 UPDATE “The data collection for this study is now complete. The researchers from the Mount Allison University Lyme Research Network would like to thank all the parents who took the time to respond to our request for letters. The letters we received were compelling and impactful, and we are grateful that you took the time to respond to Continues →
[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 →
Nov 15th, 2017 SACKVILLE, NB — Mount Allison University’s Lyme Research Network (LYRN) has released a new resource to help New Brunswickers track ticks in the region. The website – maritimetickmaps.ca – allows users to explore maps of the current and projected geographic distribution of the blacklegged tick in New Brunswick. The project is a collaboration between Mount Allison biologist Dr. Vett Lloyd and Dr. David Continues →
[CanLyme Note: CanLyme and the G Magnotta Foundation for Vector Borne Diseases have worked together for 5 years to bring this research program to fruition. This is the first step in a major thrust to aid in diagnostics, inform treatment, and bring much needed knowledge to the Canadian medical community.] CTV National News: Motivated by trajedy. July 23, 2017 After her Continues →
Australia: A Senate inquiry has recommended urgent government funding for research into tick-borne disease in Australia.
Nov. 30th, 2016 Inquiry calls for Lyme funding, research A Senate committee has recommended the federal government urgently increase funding for research into tick-borne disease in Australia and get to work on finding a treatment. Thousands of Australians claim to be suffering from tick-borne Lyme disease, but medical authorities insist it’s not possible to contract the disease in Australia. Continues →
Policy statement aims to halt missteps in the quest for certainty Monya Baker 07 March 2016 Misuse of the P value — a common test for judging the strength of scientific evidence — is contributing to the number of research findings that cannot be reproduced, the American Statistical Association (ASA) warns in a statement released today1. The group has Continues →
St. CATHARINES, ON – APRIL 15, 2015 – At sunrise on May 11, 2015, Niagara natives, 22 year old Daniel Corso and his long time friend Tanner Cookson will begin their 8000 km bike ride across Canada to bring awareness to, and raise money for, Lyme disease. The ride begins in Victoria, BC at the Terry Fox “Mile 0” mark Continues →
LymeDisease.org Publishes Largest Study of Chronic Lyme Disease Ever Conducted; Patients Suffer Poor Quality of Life and High Rates of Disability and Unemployment
Los Angeles, CA (PRWEB) April 01, 2014 Chronic Lyme disease is associated with a poorer quality of life than most other chronic illnesses, according to a newly published comprehensive patient survey. Compared to the general population, patients with chronic Lyme disease have high disability and unemployment rates, are five times more likely to visit healthcare providers and twice as likely Continues →
Researchers from Mount Allison University and veterinarians from across New Brunswick are joining forces to determine how widespread Lyme disease is in the province. They will be collecting blood samples from dogs and testing for antibodies to Borrelia, the bacteria that causes Lyme disease. Borrelia is commonly transmitted to both dogs and humans through tick bites. About 75 dogs in the Hampton Continues →
Read many peer reviewed published articles/papers on Lyme Disease. Read articles here