We have all been thrown into the world of rare disease with varying circumstances. We walk different paths…
Articles by Lori Dunham
We are all on a journey in this rare disease world. Whether we have Lambert-Eaton myasthenic syndrome (LEMS) or…
Watching a loved one suffer is unbelievably hard. Watching your child suffer and lose function is practically impossible. In my…
These last days of summer blanket us with a thick layer of humidity and unrelenting sun. For us in the…
Turning the page on the calendar is a reminder that the new school year is quickly approaching. Like most parents,…
“Kind words do not cost much. Yet they accomplish much.” — Blaise Pascal It’s that time of year again. Every…
Our world has changed over the past few years. Around the globe, COVID-19 has altered the way we all…
I’m a student of living life with intention. That means living with the end goals in mind. Whether they’re career…
Living with a chronic illness, or caring for a loved one with a chronic illness, can often be overwhelming. When…
When our daughter Grace was diagnosed with Lambert-Eaton myasthenic syndrome (LEMS), she was just 14 years old. At that…