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For someone who’s always done things on their own, asking for help doesn’t come easily.

While navigating myasthenia gravis (MG) as a new mother, Nicole learned that strength doesn't always mean doing it all on your own. She shares how learning to lean on her support system became an important part of her journey in the Untold Stories: Life with a Severe Autoimmune Condition podcast.

Discover more of Nicole’s story and others from the Untold Stories podcast: https://bit.ly/43JOEXf

Myasthenia gravis (MG) symptoms aren’t always easy to recognize, and they can change throughout the day.

This , we’re shining a light on the different ways MG may affect everyday life. 💙

Symptoms can include:
🔹 Muscle weakness
🔹 Drooping eyelids or blurred vision
🔹 Difficulty speaking or swallowing
🔹 Fatigue during everyday activities

Greater awareness and understanding helps people living with MG feel more seen, supported, and understood, while also helping encourage earlier diagnosis and continued research.

Have you struggled to find resources that are accessible and fit your needs?

Patient training resources can often be complex and difficult to access – especially when time is limited and content isn’t available in your language.

That’s why we collaborated with The Synergist and several patient advocacy groups to co-create the Patient Engagement and Capability Accelerator (PECA), a training program shaped by patient insights to make learning more flexible and accessible.

With short video modules, multiple language options, and practical, real-life examples, PECA is designed to fit into everyday life.

Start exploring the training modules: https://bit.ly/42Mo935