Category Archives: Media

Lyme disease television, newspaper, radio, and social media coverage

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Systemic Sarcoidosis Associated with Exposure to Borrelia burgdorferi in a 21-Year-Old Man

ABSTRACT Objective: Here we describe a rare case of systemic sarcoidosis in a healthy young man with neuroborreliosis as a putative trigger. Case: A 21-year-old forestry worker was diagnosed with systemic sarcoidosis involving his lungs, kidneys and skin. Additional diagnostics revealed signs indicative of a recent infection with Borrelia burgdorferi. The patient was treated successfully with prednisolone and antibiotics. Conclusion: Sarcoidosis is a multisystem 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 →

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 →

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 →

Woman walks away from wheelchair after recovering from Lyme disease

July 23, 2018 Chronicle Herald by Nikki Sullivan PORT CALEDONIA — Melissa Boutilier knows how quickly life can change after you get Lyme disease and how hard it can be to diagnose it. In July 2015, Boutilier biked around the Cabot Trail for a Heart and Stroke Foundation fundraiser. She was also getting ready to buy her first home and Continues →

Lyme Disease Patients File Federal Antitrust Suit Against Infectious Disease Specialists & Health Insurers

Nov 15th, Last Friday, 28 patients filed a federal antitrust lawsuit against the Infectious Diseases Society of America, eight health insurance companies, and seven medical doctors, Courthouse News reported yesterday, “because health insurers are denying coverage with bogus guidelines established by their paid consultants, who falsely say the disease can always be cured with a month of antibiotics.” Contrary to the often-reported claim that Lyme disease Continues →

MacLean’s magazine: How the new impatient patient is disrupting medicine

Patient activists have never been as vocal. But are they truly being heard? Anne Kingston October 21, 2017In late August, Sue Faber and Jennifer Kravis hauled close to 150 pounds of documents and scientific research into a Health Canada office in Ottawa. The two women, co-founders of Lyme-patient advocacy group LymeHope, had been granted a 15-minute audience with then federal Continues →

LANDMARK PARTNERSHIP PAVES WAY FOR CANADA’S FIRST RESEARCH FACILITY TO IMPROVE LYME DISEASE TESTING AND TREATMENT

New G. Magnotta Lyme Disease Research Lab to be Established at the University of Guelph; $1.4 Million Grant Awarded June 14, 2017 – GUEPLH, Ontario: The G. Magnotta Foundation for Vector-Borne Diseases has announced a $1.4 million grant over three years to the University of Guelph, Department of Molecular and Cellular Biology to undertake Canada’s first evidence-based translational medicine approach Continues →

Watch Mount Allison University Lyme Research Network announcement partnering with the Canadian Lyme Disease Foundation

May 5th, 2017 One of the pillars within the mission statement of the Canadian Lyme Disease Foundation is promoting research. We are pleased to announce our partnership with Mount Allison University in assisting their Lyme Disease Research Network with funding. Developing a broad capacity within Canadian universities to cope with what the government of Canada has admitted is a coming Continues →

Mount Allison University and Canadian Lyme Disease Foundation announce partnership in research.

Mount A researchers uniting expertise against Lyme disease May 5th, 2017 CumberlandNewsNow.com Fourteen researchers have come together to form the Lyme Research Network to provide a co-ordinated way to respond to the research needs of the Lyme community, to develop research that looks at the issue from new perspectives, and to share findings. The researchers represent a variety of disciplines Continues →

Listen to AM 740 radio interview with CanLyme president Jim Wilson

Zoomer AM 740 radio interview with CanLyme president Jim Wilson  May 1st, 2017 Lyme disease a serious and growing concern.  Government and medical leadership refuse to allow experts who disagree with their policies to be at the table… very dangerous for the Canadian public. Listen now, go here and scroll down to hear CanLyme interview.  

June 3rd, Ottawa: We Need To Continue To Be VOCAL

We Need To Continue To Be VOCAL The Federal Framework on Lyme Disease Conference held in Ottawa in May of 2016 allowed for people suffering with Lyme disease to finally come together. Because of the opportunity, the idea of VOCAL was formed. VOCAL – Voices of Canadians About Lyme – is a cross-Canada Lyme awareness initiative whereby each province will Continues →