A high school teacher and junior high teacher were instrumental to my diagnosis, and I finally caught up with one of them by letting them know about the booth (having not spoken since my diagnosis). There’s a slight chance I may meet her in person (for the first time) one of the days of the booth, but we will definitely have to meet soon.
Our very first collective Lyme Disease Challenge goes out to Dan and Tanner and the Ride for Lyme team (aka the Adalaine project), in a location of their choosing as they cross the continent for Lyme patients and their friend!
This challenge includes the patient they ride for that day, IF the patient is well enough. If not, we’ve got that patient covered, as we’ll be doing extra ‘bites’ on behalf of that patient in their honor.
If you haven’t, we’d highly encourage you to join this Wyoming family, and thousands of families (and teams, celebrities, news stations, and public figures) across and beyond the nation in doing so. It encourages patients, spreads awareness, and raises money for Lyme disease research. All funds raised through challenges and t-shirt sales go to ILADS.
This is an inventive, unique, and inspiring Lyme Disease Challenge from the small town of Ryegate, Montana (with a population of around 300 residents), by Carole Will Bennett. Her original posts are included here, followed by a few links and facts about the challenge.
She was also willing to share a response to a comment in one of her Facebook posts that shines some light on what she and her family have been through over many years with Lyme disease.
I’m willing to bet that the photos in her first post depict the largest collective #LymeDiseaseChallenge in the state of Montana by the time it occurred and to date. If I find I’m mistaken, I will be very surprised and you will most certainly hear about it. And if you find that I’m mistaken, please let me know about it!