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What information would you have benefited from after your MG diagnosis?
What are some things you wish you could have known after you were first diagnosed with Myasthenia gravis?
Columnist Shawna shares 10 things they wish they knew in this recent piece: https://forumsstg.myastheniagravisnews.com/columns/10-things-i-wish-knew-after-diagnosis-myasthenia-gravis/.”
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1 Reply
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Perhaps a bit more honesty about how pervasive MG can truly be.
However, it us the ” snowflake’ disease.
Living day to day
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