Wow! Now that's a lot of bad luck in the world of diagnosis. Having worked in Neurology as a Medical Assistant, I can't understand how they would be able to deduce the MG in a parkinsons patient, unless you were positive for the MG antibodies. Parkinsons, as you probably know, can be seen and diagnosed in many ways including brain MRI. There is a specific "thing" or "things" that can be seen as difinitive proof of that disease. The same cannot be said for MG. Even those with positive antibodies are not able to distiguish between the qualitative number and the severity of the disease. I have actually seen patients that had positive antibodies but had no symptoms of MG.

I also have more than one diagnosis which makes it incredibly difficult to cope. It's overwhelming for me and your situation is much more burdensome. Are any of the Parkinsons medications helping with your tremors and movements? MG weakness and fatigue is hard when I am resting so I really can't imagine how intense it must be with constant movement. Does your constant tremor contribute to your weakness or does it even matter? I mean, do your movements get less the more you move (due to the MG weakness)? I hope that question makes sense.

When were you diagnosed with each? At the same time or at different times. This fascinates me as a medical person so I apologize if this seems like the third degree.

What are some of your challenges each day and how do you think that your combination of diseases makes your struggles unique?

I'm sorry that I didn't read your "about me" in full so I didn't see if these questions could be answered there?

Take care of yourself and hugs to you.