A diagnosis of myasthenia gravis (MG) can feel overwhelming, but you do not have to navigate the journey alone. Patient advocacy organizations around the world play an important role in connecting people living with MG and their loved ones with community, education, resources and support. They can help you find others who understand what you’re experiencing, learn more about MG, access trusted resources and become more informed and empowered advocates for yourself or someone you love.
Connecting with an MG advocacy organization can be an important part of your journey. Whether you are newly diagnosed, supporting a loved one or have been living with MG for years, we encourage you to explore the organizations below and find a community that feels right for you. While each organization is unique, they share a common goal: helping people affected by MG feel more informed, supported and connected.
Explore MG advocacy organizations around the world and connect with your local community.
