Among the points that emerge from the article Jay linked in Post #154, two stand out. First, blame. If practitioners cannot identify the cause of the symptoms due to lack of training or experience in Lyme disease, some patients report finding themselves being blamed for their malaise. This, unfortunately, is found in accounts of individuals whose Lyme symptoms are mistaken for lupus, various forms of neuropathy, or depression, sometimes for years before there is an accurate diagnosis.
Clearly the physician that the subject in the foregoing article saw in Toronto got it right, and was able to help this woman.
The second takeaway is ignorance and denial by provincial health ministries. This woman and her husband reportedly spent $50,000 on treatment and medication over just three years. There is no indication in the article that she was compensated for these costs once a Lyme diagnosis was made. This is a pattern that began long before the COVID-19 crisis. There are similar stories from Lyme patients in other provinces. The article goes on to say there are 2000 reported Lyme cases in Canada.
Lyme treatment should be fully funded by provincial governments. If that were to occur, it might reveal the true Lyme disease numbers in Canada are much higher than 2000 reported cases, research might expand and, most importantly, more people might receive treatment. The status quo is a failure.
Clearly the physician that the subject in the foregoing article saw in Toronto got it right, and was able to help this woman.
The second takeaway is ignorance and denial by provincial health ministries. This woman and her husband reportedly spent $50,000 on treatment and medication over just three years. There is no indication in the article that she was compensated for these costs once a Lyme diagnosis was made. This is a pattern that began long before the COVID-19 crisis. There are similar stories from Lyme patients in other provinces. The article goes on to say there are 2000 reported Lyme cases in Canada.
Lyme treatment should be fully funded by provincial governments. If that were to occur, it might reveal the true Lyme disease numbers in Canada are much higher than 2000 reported cases, research might expand and, most importantly, more people might receive treatment. The status quo is a failure.