My Bitter & Best Friend: MG - a Column by Sarah Bendiff

I met someone who looked ravishing and well put together, with great posture, beautiful hair, and impeccable makeup, and I had my usual thought: “That’s what I would’ve looked like if I didn’t have myasthenia gravis.” But this time, something clicked, and I told myself: “This is not a…

My worst fear happened this week. The antibodies whose presence often helps diagnose myasthenia gravis (MG) disappeared in my latest blood test. My heart felt like it had stopped. Not because I felt better. Not because something changed in my body. But because I was suddenly afraid of losing…

While staying at home and resting are a go-to piece of advice when living with myasthenia gravis (MG), I’ve always loved challenging that idea and trying to live life to the fullest. But what are the real limitations imposed by MG? What’s the list of things to never do…

Anyone who knows me would completely agree that I am too talkative. It is not always easy for my entourage, but for me, it is necessary. If I keep everything inside, it drains me, and I can spend hours trapped in my thoughts, overthinking every step, questioning every decision, and…

I have sometimes been told that I must be happy to have myasthenia gravis (MG). Maybe this is because I appear too comfortable with it, or perhaps it’s easier to think I’m happy than to face the reality of living with this invisible disability. Hearing such a thing used…

Sometimes, it feels like I’m cursed with an invisible form of myasthenia gravis (MG)  whose symptoms still puzzle doctors, whose presence sometimes makes me doubt my own feelings, and whose complexity is difficult for many to grasp. Even small obstacles can feel overwhelming. No matter how hard I try…

Over the years, I’ve developed an annoying habit of blaming everything on myasthenia gravis (MG). Being aware of it sometimes makes it worse, because I catch myself doing it and still feel unable to stop. It feels like I’m slowly handing control over to MG, one excuse at a…

Any job comes with pros and cons, and working while living with a chronic disease highlights the cons in bright colors. While I often talk about my digital career, I never thought to share one of the most physically challenging jobs I’ve had with myasthenia gravis (MG): teaching.

In Algeria, we say that no one truly feels the pain of lava stones except those who have been burned by them before. It’s our way of saying that pain creates empathy, and that suffering opens the door to understanding others. When I was diagnosed with myasthenia gravis (…

I love working. I love creating. I love staying active and leaving my mark on the world. But myasthenia gravis (MG) doesn’t always enjoy accompanying me on that path, so I had to come up with a plan to keep going. The struggles are real and concrete. One of…