Life With Neurologic Lyme Disease — A Personal Reflection
The first reflection in the series: a personal look at the beginning of living with neurologic Lyme disease and what it changed about the everyday.
Lyme Disease Resources
Reflections and resources gathered from Terry Mayfield’s own experience with neurologic Lyme disease. These are personal writings and personal perspectives — written to support readers who are living with something similar, and to be honest about what the journey has actually looked like.
The series follows the experience of living with neurologic Lyme disease in Terry’s own words. Each part holds a piece of the story — the uncertainty, the small victories, and the honest accounting of what wellness and illness have asked of her.
The first reflection in the series: a personal look at the beginning of living with neurologic Lyme disease and what it changed about the everyday.
The second reflection turns toward something quieter — finding calm in the middle of a chronic illness, and learning to carry the days with more grace than fear.
Other writing that sits alongside the Lyme series in the blog — illness, healing, faith, and the everyday work of living with an invisible illness.
If you are dealing with chronic illness or seizures, you may find encouragement in the recent reflections — pieces written with honesty about healing, acceptance, and gratefulness.