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Nobody gets MG.
Until they get MG.

Chris Givens gets real about how MG has affected his life and his plans for the future in this interview.*

One relentless illness. Three unstoppable people.

A Mystery to Me

A Myasthenia Gravis Docuseries

WATCH THE TRAILER

OUR MISSION

MG RAISES QUESTIONS.
LOTS OF THEM.

MG United began as a conversation with people in the MG community. This is what we heard. And it’s why we’re here.

SEE HOW MG RESEARCH IS PUSHING FORWARD. (WE HAVE AN APP FOR THAT.)

MyRealWorld™ MG research study participants may contribute to research firsthand by recording information related to their MG diagnoses and management over a two-year period.

If you have MG, you have a story to tell.

Every person living with MG has a story that may help others in similar situations. We’d like to hear yours.

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*Paid contributor to MG United

MG United provides news and information for people with myasthenia gravis and the people who love them. But it does not provide medical advice. Always go to your physician, neurologist or other appropriate health professional for individual guidance, diagnosis and treatment.

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