62. The role of patient organizations with Mario Levesque
Lyme patients working together to get the healthcare they need.
Exploring the politics, activism and history of Lyme disease through conversations with philanthropists, politicians, authors, Lyme-literate physicians and more
Lyme patients working together to get the healthcare they need.
Harnessing the power of words to communicate, advocate, and heal.
Twenty years and counting: CanLyme continues to support patients through research, education and advocacy.
This week Sarah is joined by Dr. Shelley Ball, an evolutionary ecologist, fellow of the Royal Canadian Geographical Society, and Founder and President of Biosphere Environmental Education, a social enterprise focused on connecting people with nature.
In this episode, Sarah speaks with Rossana Magnotta, who established the G. Magnotta Foundation in honour of her late husband, Gabe, who passed away after a courageous battle with Lyme disease. The G. Magnotta Foundation leads scientific research into Lyme disease at the University of Guelph in Ontario. Rossana tells Sarah that Gabe was an…
In today’s podcast, Sarah is joined by Jim Wilson, founder and President of CanLyme — the Canadian Lyme Disease Foundation. After contracting Lyme disease 30 years ago in Nova Scotia, Canada, Jim dedicated his time and energy to improving the lives of Lyme patients and their families, helping to bring a balanced perspective of Lyme disease to the forefront.
As Dr. Maloney says, “Research is our way out of this.” This is our kind of expert leading the way in the field. In today’s podcast, Sarah explores a comprehensive (and free!) online education program designed for healthcare professionals, which was founded by Lyme disease expert, Dr. Betty Maloney.
In today’s podcast, Sarah talks about ticks, Lyme disease and climate change with investigative reporter Mary Beth Pfeiffer. She lives in New York State, an area of the US which is highly endemic for Lyme disease, and has been investigating this disease for the past eight years.
Advancing a vision for research in Lyme disease and translating research from bench to bedside.
In this episode, Sarah speaks with another champion for Canadians living with Lyme, Green MP Elizabeth May. She describes how she first learned about the severity of Lyme disease when speaking to a woman from Pictou, Nova Scotia who required a wheelchair for mobility. After moving to British Columbia, Elizabeth met others who were experiencing life-altering illness due to the tick-borne diseases.
In this episode of Looking at Lyme, Sarah speaks with Internal Medicine Specialist and Canadian Lyme expert, Dr. Ralph Hawkins. Dr. Hawkins has been treating Lyme patients in Canada for many years, gaining a wealth of knowledge about the disease. He recounts his introduction to the shortcomings of Lyme disease testing in Canada while treating…
In this episode, Sarah interviews an Infectious Disease Physician who has treated Lyme patients in the US state where Lyme disease was first identified.
Funding grants for healthcare practitioners are available now!