Teen Lyme Activist Thanks Senators Susan Collins & Tina Smith for Passage of Kay Hagan Tick Act
by Press Release from Outbreak News Today on (#4WXJ7)
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 now law, marking a historic moment for people who suffer from Lyme and other tick-borne diseases. The legislation adds $150 million in new federal funding to fight ["]
The post Teen Lyme Activist Thanks Senators Susan Collins & Tina Smith for Passage of Kay Hagan Tick Act appeared first on Outbreak News Today.