Activists call for provincial Lyme disease strategy
May 6th, 2015 Jessica Bell from the Ontario Lyme Alliance and Jeanne Pacey who suffers from Lyme disease, spoke to CityNews’ Francis D’Souza. Watch City News
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May 6th, 2015 Jessica Bell from the Ontario Lyme Alliance and Jeanne Pacey who suffers from Lyme disease, spoke to CityNews’ Francis D’Souza. Watch City News
Cindy E. Harnett / Times Colonist May 10, 2015 Retired anesthesiologist Dr. Martin Rodgers was treated with two days’ worth of antibiotics and told not to worry after he showed his family doctor a classic bull’s-eye rash caused by a tick he extracted from his navel. That was three years ago this July. Now Rodgers, 74,…
Watch touching video of a Grandpa who started running for Lyme on January 2nd, 2015 and has logged over 1000 km since then. He keeps on running to help his grandson and others stricken with Lyme and unable to get help in their province. Watch video
May 6, 2015 /PRNewswire-USNewswire/ — It’s been forty years since Lyme disease was first recognized in the US− when researchers studied an unusually large number of children diagnosed with juvenile rheumatoid arthritis around Lyme, CT. Their investigation was initiated through a phone call by a mother with sick children, Polly Murray, who noticed the anomaly…
By LAUREL BROWN FOR MAILONLINE PUBLISHED: 22:53 GMT, 7 May 2015 | UPDATED: 22:59 GMT, 7 May 2015 For close to three years, Real Housewives Of Beverly Hills star Yolanda Foster has dealt with chronic Lyme disease. Based on an Instagram photo the 51-year-old former model posted on Thursday, however, she has not given up…
by Kendra Wong – Victoria New posted May 7, 2015 at 1:00 PM Two Ontario cyclists will be starting their 8,000-kilometre cross-country cycling trip in Victoria next week to raise awareness of lyme disease. Daniel Corso and Tanner Cookson from St. Catharines, Ontario are riding from Mile 0 in Victoria to St. John’s Newfoundland for a…
Council proclaims May as Lyme awareness month, and, “Council sucks limes” for Lyme. For the video of the meeting relating to the proclamation and challenge click below and then go to Lyme Disease Awareness – Lyme Sucks Challenge Watch here
By Lauren McNabb Senior Reporter/Anchor Global News – May 1st, 2015 WINNIPEG – At this time of year they could be as small as a poppy seed, but no matter the size, a black-legged tick can carry a potentially nasty bite. May is Lyme Disease awareness month and it is one of several tick-borne diseases doctors say an…
Dear Abby: Speedy diagnosis essential for treatment of Lyme disease To be published in newspapers May 1st in Canada Dear Abby: May is Lyme disease awareness month. I’m a longtime Canadian reader who has suffered from it for many years. More than 300,000 people are infected by this tick-borne illness every year, yet people know…
Hopkins physician Paul G. Auwaerter, MD, has told the Allentown Morning Call that Lyme patients invent ideas about what ails them. “When is a Johns Hopkins School of Medicine researcher no longer competent to conduct research and treat patients?” asks Cutler, who has been battling Lyme disease for more than nine years. “When he ceases…
Staying informed can be your best . By Jane Doucet WITH THE WARM weather arriving, many Canadians will be spending time camping, hiking, and horseback riding. While it’s wonderful to watch Mother Nature spring to life, less desirable creatures are also stepping up their activity at this time of year. Read full article
BY DAN FUMANO, THE PROVINCE APRIL 22, 2015 In 2013, a clinic heralded as the first of its kind in Canada opened in Vancouver with a mandate to diagnose and treat Lyme disease in B.C. It was a moment of great hope and optimism for many chronic Lyme sufferers in B.C. But two years later,…
[CanLyme note: Dr. Gerald Evans’ comments in the article linked below are a great example of why patients Canada-wide are so disgusted with Infectious Disease doctors. Lyme disease patients are doctors, lawyers, microbiologists, engineers, labourers, truckers, plumbers, house wives and husbands, and children. He paints us as being naive, incapable of making sound health care judgments…
On April 24th, 2015, the Canadian Lyme Disease Foundation’s founder, Jim Wilson, was proud to have his brother, John Wilson, and oldest daughter Candra Wilson make their challenges to others to take the Lyme Sucks Challenge in the effort to raise awareness of the disease, and increase funding for a very necessary and long overdue…
Because the patients are contested “They immediately may send the patient to test for all manner of serious immune and neurologic disease, not realizing that Lyme disease itself may cause profound immune and neurologic conditions if it is not treated at once.” Read full article
The Canadian Lyme Disease Foundation is dedicated to promoting research, education, diagnosis and treatment of Lyme and associated diseases.