My goal is to minimize MG effects, even if it means not doing certain things where I may overexert myself. 

My MG is under control and doesn’t bother me that much, and I want it to stay that way.

My goal is to be able to make plans and keep them so I can do more of what I love. 

My MG isn’t great, but I’m content with things staying this way as long as I don’t lose ground. 

I do not have MG.

I can speak normally.

I have intermittent slurring or nasal speech.

I’m constantly slurring or having nasal speech, but I can be understood.

It’s difficult for others to understand my speech.

I can chew normally.

I experience fatigue when chewing solid food.

I experience fatigue when chewing soft food.

I need to use a gastric tube.

I can swallow normally.

I have rare episodes of choking.

I have frequent episodes of choking that make dietary changes necessary.

I need to use a gastric tube.

I can breathe normally.

I experience shortness of breath when exerting myself.

I experience shortness of breath when at rest.

I depend on a ventilator to breathe.

MG has no effect on my ability to complete these activities.

I can do both activities with some extra effort but don’t need any rest periods to help.

I need rest periods in order to complete these activities.

I’m unable to do at least one of these activities.

MG has no effect on my ability to do this.

MG has a mild effect on my ability to do this. I sometimes need to use my arms to get up.

MG has a moderate effect on my ability to do this. I always need to use my arms to get up.

MG has a severe effect on my ability to do this. I always need assistance to get up.

No, I don’t experience double vision.

Yes, but not daily.

Yes, I experience it daily but not constantly.

Yes, I experience it constantly.

No, I don’t experience eyelid droop.

Yes, but not daily.

Yes, I experience it daily but not constantly.

Yes, I experience it constantly.