Imagine never feeling well and having doctors diagnose you with a different illness each time you sought help. Imagine health providers blaming your mental state for a disease that you would later discover had been the cause of your suffering all along. And then imagine realizing that your infection had been passed to your kids, and this particular disease is so not funded in Canada, making accurate diagnosis and treatment extremely limited. Such was the case with Tanis Michelsen, who has since become an advocate for the recognition and treatment of lyme disease.
Jill Amery
Jill Amery is a mom of 2 small boys and the Publisher of UrbanMommies, a stylish digital lifestyle magazine filled with fitness, style, health, recipes and savvy mom advice to help you through pregnancy, birth, and raising your kids.








