Sharing our story is one of the most important things we can do to spread awareness of Lyme disease.
For my most recent article on the Global Lyme Alliance blog I asked four wonderful Lyme bloggers to weigh in on the question, "What is it like to have an illness no one believes in?"
Christina of Lady of Lyme, Kami of Living Grace, Victoria of Lemons 'N Lyme, and April of Happy Healin' Vegan, all had interesting and heartfelt responses to this question.
You can read the full article here:
What It's Like to Have an Illness No One Believes In
If you're reading this blog you may have Lyme or love someone who has Lyme. What's it like for you to have an illness no one believes in? Leave a comment and spread awareness.
"As long as I’m alive, I will continue to try to understand more because the work of the heart is never done." - Muhammad Ali
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.