The struggle seronegative myasthenia gravis patients face for diagnosis and treatment.

Rare Disease Day happens once a year, but you can bring awareness to myasthenia gravis any day of the week!

Illuminating the support rare disease patients need 365 days of the year.

Rare Disease Week starts on February 28. Learn how you can advocate for people with MG.

Janet Myder was a Dedicated MG Volunteer.

For Brenda Colmenares, an MG diagnosis set her on a path of rare disease advocacy and awareness.

MG Advocates Describe Their Experiences During Rare Disease Week

Volunteers Ensure Political Leaders Understand the Challenges of Rare Diseases like Myasthenia.

Lenora “Lynn” Waltz was an amazing advocate for the myasthenia community, with an inspiring story that touched so many people.

Drea Carbone began her MG advocacy almost as soon as she was diagnosed and she hasn’t slowed down since.