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Discover how patients navigate rare and serious diseases with resilience, support, and hope—and how their voices are driving change for others.

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Swimming Through the Invisible: Tia Chakrapani’s Journey with Myasthenia Gravis
At 14, competitive swimmer Tia Chakrapani spent eight months being told her symptoms were anxiety or asthma. After finally receiving her myasthenia gravis diagnosis, she's now helping other young patients get the care and answers they deserve.
Upsetting the MG Status Quo: Shawna Barnes
Meet Shawna Barnes: An MG Patient Who Refuses to Falter
Welcome to the Family: Victoria’s Journey with gMG
Told for seven years that her bloodwork was normal, Victoria faced disbelief before being diagnosed with antibody-negative generalized myasthenia gravis.
Smiling Halfway, Living Fully: Layla’s Journey with gMG
Diagnosed with myasthenia gravis at 18, Layla now navigates life with renewed purpose as a community manager and advocate through @sonriendoamedias.
Sonriendo a medias, viviendo por completo: el camino de Layla con Miastenia Gravis Generalizada
Diagnosticada con miastenia gravis a los 18 años, Layla hoy comparte su experiencia mediante @sonriendoamedias y vive con propósito como community manager.
I Just Know My Kid: Kari’s Journey Navigating Her Son’s gMG
Kari works in accounting, not medicine. One day she had to sit down at her computer and work out what was wrong with her son. She was right.

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