Lyme Action Group, a southern-Ontario based advocacy group seeking improved Chronic Lyme Disease public policy in Canada, held a press conference at the Ontario Legislature on 7 November 2008. Participating were Helke Ferrie (Part 1, introduction), patient Janet Mitchell (Part 2), patient Dr. Graham Kucan (Part 3), patient Karin Klouman (Part 4), and Dr. Jozel Krop (Part 5). For more info please visit: LymeActionGroup.blogspot.com
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Lyme Action Group Press Conference – Part 5: Dr. Jozef Krop5 comments to Lyme Action Group Press Conference – Part 5: Dr. Jozef KropLeave a Reply |
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I am so grateful that men like this exist…. a man who serves to help heal … and is BOLD enough to stand up against the powers against him… may God’s richest blessing be upon him …
We may have better tests in the U.S. but they still are only 50% accurate. Even in the U.S. you are denied the diagnosis when you do have Lyme disease. Igenex labs in the U.S. is one of the few labs that tests all of the bands, whereas the labs used by most physicians leave out many of the Lyme specific bands making it more difficult for you to be positive. This is wrong. I hope another Canadian physician will take this doctor’s place. We need more LLMDs.
This is happening in the U.S. as well. You can thank the Infectious Diseases Society of America (IDSA) for starting this witch hunt against doctors with integrity. I hold the IDSA largely responsible for the disinformation that is being sent around the world regarding chronic Lyme. The IDSA are present day Nazis — Lyme Nazis.
I can’t even start to watch this.
This is a crime. Doctors are being persecuted for treating patients with chronic Lyme disease. If anyone is interested, I wrote a Lyme disease brochure with the help of 2 Lyme specialists and would be happy to email to anyone. Great resource information that includes some of the many Lyme organizations out there. Please, everyone get involved with the fight against Lyme disease !!