Guest Voices

When I sat down to write a column about parenting with myasthenia gravis (MG), I had to give it a lot of thought. So much has changed for me since my diagnosis two years ago. I’m a single parent. My daughter was conceived with a donor, so it’s…

“You can’t do anything about the length of your life, but you can do something about its width and depth.”  — Anonymous These are wise words from an anonymous writer. Following these words and disregarding my myasthenia gravis (MG)-related restrictions, I decided to join my family on a trip…

A diagnosis can change your life, but it doesn’t have to define it. For me, living with myasthenia gravis (MG) doesn’t just mean learning how to manage the disease. It has helped me ask questions, notice patterns, and even become something I didn’t expect: a patient researcher.

Sixteen years ago, when I was diagnosed with myasthenia gravis (MG) at the age of 12, I was very active. I played sports, including volleyball, until I had to quit because double vision made it impossible. I didn’t like giving up sports, but since I was a teenager and…

Everything began when I was 12 years old, still in school, and suddenly started seeing double. I didn’t understand what was happening, and it scared me. After school, I told my parents, who immediately took me to our general practitioner (GP) and arranged a visit with an optometrist. Both the…

Chronic illness rarely announces itself with clarity. Instead, it unfolds quietly, often disguised as fatigue, stress, or temporary discomfort. My experience with myasthenia gravis (MG) began in October 2020, shortly after giving birth. It was a period I had expected to be defined by recovery and bonding. Instead,…

Note: This column describes the author’s own experiences with Mestinon (pyridostigmine bromide). Not everyone will have the same response to treatment. Consult your doctor before starting or stopping a therapy. I started noticing slight muscle weakness about six months before I began to seriously think that something might be wrong.

“You will never amount to anything” and “useless” are words that were etched into my mind since I was very young. Difficulty breathing, chewing, swallowing, and speaking are just some of the symptoms I experience every day. Because of these, I once came close to believing those words. Maybe…

Those of us with myasthenia gravis (MG) often discuss the symptoms we experience and spend considerable time planning around them and managing their impact on our daily lives. MG literature is full of strategies for coping with muscle weakness and poor vision or avoiding triggering our condition, but we…

Tears gathered in my eyes as I read the disappointing visit summary from a neurology appointment. Being a seronegative myasthenia gravis (MG) patient, I’m leery about seeing neurologists for fear they will dismiss the diagnosis that took years for me to get, but I left the appointment pleasantly…