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New Brunswick resident Stephanie Stoneleigh has had enough and wants the News Brunswick health care system to wake up to the fact that Lyme disease is occuring in numbers far above what is being reported. Her published letter to the editor spells out the issues.
Recently, the Montreal Gazette newspaper published this article … According to the Montreal Gazette we are scaring people by telling them we have a serious and growing problem, a problem echoed by the Public Health Agency of Canada. https://montrealgazette.com/health/opinion-lyme-disease-is-very-real-but-its-no-epidemic We asked for equal print space to write a rebuttal. We were refused because the editor…
Editor’s note: Pamela Weintraub is the author of “Cure Unknown: Inside the Lyme Epidemic” (St. Martin’s Press), winner of the 2009 American Medical Writers Association book award, and executive editor of Discover magazine. Follow her on Twitter: @pam3001 (CNN) — Our nightmare began in 1993 after we moved from the city to a house down…
December 31, 2014 Belleville News By Diane Sherman Elizabeth May, leader of the Green Party, MP for Saanich-Gulf Islands, introduced Bill C-442, June 2012, to stimulate debate about prevention, diagnosis, treatment, and research on Lyme disease, a disease caused by insect bites, primarily ticks. December 16 the bill became law: An Act respecting a Federal…
[How many more just are left to die in Canada? Not a great tourism advertisement for our country and it’s alleged great medical system] NEW DELHI: Doctors at a private hospital here have given a new lease of life to a man declared “near brain dead” by a hospital in Canada. Asok Debnath, an IT professional…
Experts say precaution is crucially important May 17th, 2019 by Anam Khan, GUELPHTODAY.com As the warmer weather finally sets in, the tick season brings on a serious cause for concern as Lyme disease cases in Canada rapidly rise. The problem? There is no perfect laboratory test that can tell you whether or not you have…
[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…
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I’m suffering from chronic Lyme disease I have spent over 50 thousand dollars trying to get better, and lots of it went to the States, first of all why can’t canadian doctors treat you, and is it not better if our money stayed this side of the border…..I’m sick and tired of not being able to get help, at the moment I have 2 frozen shoulders, and of course when you mention lyme to the doctors, they move on and start talking to you about fibromyalgia and so on, it’s been over 6 months, I’ve been sent to an orthopaedic surgeon, physiotherapy and on my own and out of my pocket have gone to acupuncture and chiropractor treatment and still I’m in a lot of pain…..