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.

Articles by Lori Dunham

My Daughter Receives Evusheld to Protect Against COVID-19

Every six months, my daughter Grace and I go to the children’s hospital for her Rituxan (rituximab) infusions. This has proven to be one of the most effective treatments for Grace after she was diagnosed with Lambert-Eaton myasthenic syndrome at age 15. The Rituxan infusions are usually preceded…

How the LEMS Community Inspires Others by Giving Back

My husband says traveling is in his blood. He grew up overseas, so it was only natural that we would often travel to his “home” early on in our marriage. When we started having kids, we learned all the tricks of traveling with toddlers. Thanks to the U.S. Navy, we…

Coping With Surprises in Life With a Rare Disease

I don’t like surprises. Almost every Christmas, my husband and I end up sharing what we bought for each other long before we find the gifts under the Christmas tree. Along the same lines, I would much rather plan for and anticipate a vacation than be surprised with one. So…

How to Stay Safe Despite Physical Limitations

When my daughter Grace was 10, she requested a taser for Christmas. I’m not sure what prompted this request or why she felt the need for one. Regardless, she did not find a taser under the Christmas tree that year. However, as she grew into a young teen, Grace continued…

While You’re Being Thankful, Make Sure to Laugh a Little, Too

Traditionally, November is when we give thanks. With Canada and the U.S. celebrating Thanksgiving in October and November, respectively, it’s a season when many of us turn our attention to gratitude. That’s even true for us in the rare disease community. We face many hurdles throughout the year; life with…