It seems that Lambert-Eaton myasthenic syndrome (LEMS) likes to keep us guessing. Two years after our daughter Grace’s…
Lori Dunham
Lori Dunham and her family have lived all over the world thanks to the U.S. Navy. She has a degree in human resources but enjoys writing to encourage and inspire others. When her daughter Grace was diagnosed with Lambert-Eaton myasthenic syndrome at age 15, Lori sought community and encouragement from those walking a similar path. Lori’s mission in writing is to inspire and encourage those who find themselves in the role of caregiver. When she is not writing or homeschooling her two youngest, Lori enjoys reading, baking, and spending time with family. Currently they live in Jacksonville, Florida.
At Bionews we’re committed to providing the most accurate, relevant, and up-to-date reporting for our patient communities. Our goal is to ensure that everyone has access to disease-specific information that is both trustworthy and easy to understand. You can read more about our editorial policy here.
Articles by Lori Dunham
For the first year after our daughter Grace was diagnosed with Lambert-Eaton myasthenic syndrome (LEMS), our schedule was…
As the mom of a 16-year-old daughter with a rare disease, I’ve had to learn how to…
If anyone had told me three years ago how our life would look today, I would not have…
We are living in unprecedented times involving a pandemic and political and social unrest that has been…
The paths of those affected by Lambert-Eaton myasthenic syndrome (LEMS) hold many twists and turns.
Eeyore from “Winnie the Pooh” has never been my favorite character. For most of my life, I could…
Many people with Lambert-Eaton myasthenic syndrome (LEMS) wait an extremely long time for a diagnosis. Our family waited…
I have often said that we would try any treatment if it meant more mobility, strength, and health…
I consider myself a pretty resilient person. My husband is in the U.S. Navy, and I can accommodate…