I am so pleased to announce that I will be a contributor on Lymeology:
"Lymeology is an editorial website dedicated to educating, empowering, and inspiring Lyme and invisible illness patients."
I'm listed as a "Lymologist," which is amazing. Check out my bio.
My 1st post on the site is.This is something I've struggled with since my diagnosis. I hope these tips help others know what to say:
5 Ways to Answer the Question 'How Are You Feeling?' If You Have Lyme Disease
I will be guest posting there from time to time, and I'll keep posting the links here.
Make sure you check out all the great articles on Lymeology, and if you are a Lyme blogger or patient consider submitting one of your own.
"By reaching and stretching and trying new things, you’ll expand your life experiences and, in turn, your confidence." - Dr. Phil McGraw
I'm Kerry and I was diagnosed with chronic Lyme disease in 2016. This is a positive space for those of us coping with Lyme disease and other invisible illnesses.