Twin Cities Lyme Foundation has partnered with Coin Up, the easy, safe and fun way to support Lyme awareness and proper diagnoses all year long. With a one-time set-up, you can start rounding up your purchases to the nearest dollar and the difference can make a real difference in the lives of those affected by […]
TCLF founder shares her journey
Weather is factor in tick population
Fall sports another risk for Lyme
Founder spouse and foundation board member shares the Lyme story nationally
Fall means ticks – TCLF raises awareness at state fair
Lisa Najarian shares information about Lyme disease on a Twin Cities podcast. This was a segment in “The BS Show,” which can be downloaded at thebsshow.net as well as iTunes, Stitcher and playerfm.
There’s nothing Gelfand knows better than disease. It’s just that medical research tends to take place before noon. It’s a shame, because Lyme needs all the research it can get. You may not be a Gelfand, but you can still help by donating to the Twin Cities Lyme Foundation. Lyme, not Lyme’s.
Lyme disease has become one of the fastest growing epidemics in the nation. Join Lisa Najarian as she relates her story of battling Lyme disease and how she has started the Twin Cities Lyme Foundation in response.
Twin Cities Lyme Foundation founder Lisa Najarian, with husband Pete, shares her journey and more about the launch of the organization.
Member of Minnesota’s own Najarian family, living with Lyme disease, launches Twin Cities Lyme Foundation