All the letter-writing, phone calls, meetings with members of Congress and the federal government are paying off for 15 year old LivLyme Foundation founder Olivia Goodreau. The Kay Hagan Tick Act is...

By NewsDesk  @infectiousdiseasenews Colorado teenager Olivia Goodreau has garnered support from some of the world’s top scientists as a leading advocate for Lyme disease awareness and research funding....

13-year old Olivia Goodreau has been living with Lyme disease for half her life. She joined me today to tell her story from the tick bite to a myriad of symptoms to visiting 51 doctors before being diagnosed...