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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…
Lyme disease can masquerade as MS, ALS, even dementia and its numbers are growing tenfold. So why is Canada lagging behind in treating and diagnosing it? by Anne Kingston [March 2014] For decades, Gabriel Magnotta, the well-known Ontario wine-industry firebrand, went hunting with a group of friends. These expeditions took them into the wilds of…
The Canadian Lyme Disease Foundation is dedicated to promoting research, education, diagnosis and treatment of Lyme and associated diseases.
