Living with Myasthenia Gravis (MG) means navigating constant uncertainty. Symptoms flare out of nowhere, your body decides its own rules, and rest becomes more essential than optional. But a question that follows me is: Why me?
Moving into a new home is often described as a fresh start. But when you live with myasthenia gravis (MG), it can feel more like a marathon you didn’t train for.
Myasthenia Gravis (MG) weakens your muscles, especially upon exertion. Side effects, other diseases, and additional health conditions can happen after you’re diagnosed. One of these problems is how it can impact your sleep.
Living with Myasthenia Gravis (MG) is like budgeting energy on a card with an unpredictable limit. Some days, I make it to the end of the day with credit to spare. Others, I’m overdrawn by 10 a.m. and paying in symptoms.
When I was first diagnosed with Myasthenia Gravis (MG), I focused on the obvious: My immune system. I assumed that if I could manage that, everything else would fall into place.
If you've followed my blog for long, you may know one of the main symptoms of myasthenia gravis (MG) is difficulty swallowing. Yes, your throat and tongue are muscles.
