Latest Blog Posts from Misha Grayson Coleman

Why It Matters How Myasthenia Gravis Is Portrayed in Media

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.

By Misha Grayson ColemanOctober 29, 2024
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When MG Unlocks Your Creativity

When MG Unlocks Your Creativity

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.

By Misha Grayson ColemanOctober 15, 2024
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What I've Gained from Living with MG

What I've Gained from Living with MG

Living with myasthenia gravis (MG) isn’t something I anticipated. When I first received my diagnosis, my world tilted on its axis.

By Misha Grayson ColemanOctober 8, 2024
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The Power of Pets in Living With MG

The Power of Pets in Living With MG

There's a special kind of comfort that comes from being around animals, especially when you face the unpredictability of Myasthenia Gravis (MG).

By Misha Grayson ColemanSeptember 24, 2024
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How Weather Affects MG

How Weather Affects MG

Living with Myasthenia Gravis (MG) is like trying to predict the weather—unpredictable and sometimes downright frustrating.

By Misha Grayson ColemanSeptember 10, 2024
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Advocating for Yourself When You Live with MG

Advocating for Yourself When You Live with MG

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.

By Misha Grayson ColemanAugust 27, 2024
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