Why It Matters How Myasthenia Gravis Is Portrayed in Media
Living with MG is a journey shaped by resilience, adaptability, and a daily dose of humour in the face of unpredictability.
Misha Grayson Coleman was diagnosed with myasthenia gravis, a rare neuromuscular disease, in 2021. Despite this diagnosis and her life being turned upside down, she is determined to live her life to the fullest and to spread awareness about the condition to help others who may be going through similar struggles. Not only is she a dog mom, but she's also a fashion and travel influencer as well as a health enthusiast. She dedicates her time to researching, learning, and sharing the best ways she's found to manage her condition with the goal of reaching remission. Connect with her here.
Living with MG is a journey shaped by resilience, adaptability, and a daily dose of humour in the face of unpredictability.
Living with Myasthenia Gravis (MG) means dealing with changing symptoms. On tough days, it can feel like you're at the mercy of your body. But symptom-heavy days can be opportunities to tap into creativity and mindfulness.
Living with myasthenia gravis (MG) isn’t something I anticipated. When I first received my diagnosis, my world tilted on its axis.
There's a special kind of comfort that comes from being around animals, especially when you face the unpredictability of Myasthenia Gravis (MG).
Living with Myasthenia Gravis (MG) is like trying to predict the weather—unpredictable and sometimes downright frustrating.
Living with myasthenia gravis (MG) has been a relentless journey of self-advocacy. From Day One, I realized getting proper care means constantly fighting to have my voice heard.