The Symptom-Searching Rabbit Hole: When Google and AI Help, and When They Don’t
I have a slightly complicated relationship with researching my health online. On one hand, it has helped me understand myasthenia gravis (MG) ...

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.
I have a slightly complicated relationship with researching my health online. On one hand, it has helped me understand myasthenia gravis (MG) ...
I was watching a story on Instagram recently from a disabled woman who uses a wheelchair, and I haven’t really stopped thinking about it since ....
When people think about living with myasthenia gravis (MG), they often picture the obvious things: medications, hospital appointments, flare-ups, or the bigger lifestyle changes that come with a chronic illness.
When I was diagnosed with myasthenia gravis (MG), I don't remember being handed an instruction manual. Looking back, I think someone forgot to include it ....
After being diagnosed with myasthenia gravis in 2021, I joined support groups, read stories online, and connected with plenty of people through social media who also had the condition. But I had never actually met another person with MG in real life, until recently ....
Myasthenia gravis already feels like living with an unpredictable energy system. So burnout in this context is not just emotional exhaustion. It also becomes physical ....