I recently did an interview with Victoria of the blog Lemons 'N Lyme.
She offered me the opportunity to do a guest post on her blog, so of course I agreed.
I wanted to write something for the newly diagnosed, because I think that is a very scary time for Lyme patients, as it was for me. I thought about some of the things it would've been nice to hear when I started treatment and put it together in a post along with some friendly advice.
Here is a link to my post on Victoria's blog:
Advice for the Newly Diagnosed Lyme Disease Patient
Now spend some time looking through Victoria's blog. She has some great recipes. I can't wait to try the Creamy Cauliflower Sauce with Coodles (cucumber noodles). My two favorite veggies together in one delicious meal.
Share a comment below on what you wish you'd known when you were first diagnosed.
"I'm not telling you it's going to be easy. I'm telling you it's going to be worth it." - Art Williams
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.