![]() Groundbreaking news! ILADS Guidelines listed on Public Health Agency of Canada website! Canada is a world leader! The Public Health Agency of Canada has now listed the International Lyme and Associated Diseases Society (ILADS) treatment guidelines - on their website - as one set of evidence-based treatment guidelines for Lyme disease. More to come, but we wanted to get the news out! To see for yourself: Scroll to the bottom of the page (link) below - under More Information and International Treatment Guidelines https://www.canada.ca/en/public-health/services/diseases/lyme-disease/health-professionals-lyme-disease.html#a3 Thank-you to all the tireless Lyme advocates from across Canada who have been pushing for this important recognition. Let's help more Canadians! Please sign, comment and share our Canadian Lyme Petition! https://www.change.org/p/minister-petitpas-taylor-ticking-lyme-bomb-in-canada-fix-canada-s-lyme-action-plan-now #canlyme #lymehope #lymeadvocatesworkingtogether
9 Comments
6/6/2018 09:53:45 am
It has come along way .. But still not helping long term Lyme. Still have to leave Canada for treatment .. And no help paying the bills .. Nothing for travel or treatment ..
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Carmelina Crudo
6/6/2018 04:46:15 pm
I have Benn so ill for years and each year I got sicker and sicker to the point of complete debilitating disability, bed ridden, home bound. Every test for Lyme Disease came back negative until I went to an Internist and Naturopathic Doctor who specializes in Lyme Disease by the advice of my MD. I had to take out a small mortgage that I couldn't afford to pay for these tests that went to Germany and California and results came back astounding me with how severe my Chronic Lyme Disease and it's co-conditions of Fibromyalgia and Chronic Fatigue Syndrome or Myalgic Encephalomyolitis. Confirmed with 6 different infections caused by ticks in my central nervous system and brain and parasite, heavy metal poisoning , mold, Candida and yeast overgrowth everywhere, 7 live viruses including Epstein Barr Virus and a form of Malaria and the list goes on . Final diagnosis .... MULTIPLE SYSTEM INFECTIOUS DISEASE SYNDROME aka severe Chronic Lyme Disease and it's co-conditions. I feel like I'm dying a slow death and have lost my life, health, income, independence , and dignity. The testing in Canada is appalling as I was told I was negative for Lyme Disease 5 times over the last decade. This cannot go on. We are dying and the treatments are all out of pocket because the CDC has regulated what doctors can and cannot do to help us. Antibiotics are not enough to treat our multiple systems infections and viruses and mold and toxins. Things needs to change NOW. We cannot afford the costs of integrative medicine....this should be the norm and covered by our governments as Chronic illnesses are becoming more and more complex by environmental changes, food industries GMO'S, over processed foods and agriculture stripping goid nutrients from our diets. People are committing suicide at an alarming rate because we can't live like this any longer. Decades of being so sick with no answer is not right.
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Theresa
4/7/2020 02:23:36 pm
Where did you go in Germany and California to do this additional testing? Is there no where local in Ontario?
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Hanna
10/7/2018 07:04:22 pm
I scrolled to the bottom of the page but did not find the "international treatment guidelines". How might I obtain the international treatment guidelines on lyme?
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