December 2014

The Senate’s unanimous passing of Bill C-442, An Act to Create a Federal Framework on Lyme disease, provides hope and promise for both current and future Lyme disease patients. The following article, entitled “No Coordination of Care in Canadian Health Care,” published recently in The Medicine Hat News, describes the struggles that are all-too typical for so many Canadians

While many of the points addressed in the Bill have been agreed upon by all stakeholders at the meeting, certain wording within the bill has created concern for infectious disease specialists, who argue that it suggests support for ‘pseudo-science’ treatment guidelines, while dismissing current evidence-based guidelines put forth by the Infectious Disease Society of America