LEMme Tell Ya - a Column by Dawn DeBois

When you take a plethora of medications to manage multiple chronic conditions, it’s only a matter of time before some of the side effects catch up to you. I’ve battled chronic migraines since college. I remember my first migraine hitting me while I was living in my freshman dorm. I…

When I checked into my last day of immunoglobulin therapy last week, I sat next to another patient in the waiting area. She looked over at me and said: “I’ve read all of your blog articles. It’s nice to have them, because you really do understand what we go…

Five years ago, Will Schuller was thoroughly enjoying his senior year in high school when he began experiencing symptoms of Lambert-Eaton myasthenic syndrome (LEMS). He was in the marching band, running 25 miles a week, and taking four Advanced Placement classes and one honors class when his life suddenly changed.

Spontaneity is what I miss most about my pre-LEMS life. No longer can I hop in the car and go to a concert, the beach, or a quick weekend away without planning around meds and treatment schedules. Even with the best-laid plans, I find myself pulling over to make sure…

I recently attended the first meeting of the Northern New England Myasthenia Gravis Support Group in Portland, Maine. The event was hosted by a pharmaceutical company to promote its new product. However, I didn’t let that deter me. I wanted to meet other local myasthenia patients like myself. The…

I used to pass out at the sight of blood. As a toddler, I saw the blood from my mother’s suicide attempt. The images from that night will forever be 10-second flashbacks in my brain. Fainting was my body’s way of protecting myself from more trauma. As I grew older,…

Did you know that October is “National Disability Employment Awareness Month“? I hadn’t realized it until midmonth, though I’m legally disabled and employed as a writer. This year’s theme, “The Right Talent, Right Now,” jumped out at me as thoughts swirled in my head about having a month dedicated…

We’ve all been there. Our doctors suggest a new treatment for our rare disease, and after consulting with other patients through social media, we decide that the option is too scary. I did this with intravenous immunoglobulin (IVIG) replacement therapy. For more than a year, I held my neurologist…

This month’s “’LEMme Tell Ya’ Patient Stories in Their Own Words” features a Lambert-Eaton myasthenic syndrome (LEMS) patient I am grateful to call my friend. Price Wooldridge offers encouragement to newly diagnosed patients, and doesn’t hesitate to brainstorm with someone who is struggling with symptoms. His advice is…

One of the first Lambert-Eaton myasthenic syndrome (LEMS) patients I had the pleasure of meeting in real life was Romy Braunstein. Romy is taller than me, which is no small feat because I am pushing 6 feet. Her personality is larger than life, and her sense of humor has…