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@colleenyoung

Hi @wcburns2, I expanded the title of your discussion to reflect your question and included it in the Eye Conditions and Visiting Mayo Clinic support groups as well. I'm tagging fellow members like @ginnycoleman @Erinmfs @laurievr @shellyleon_dd @skhollandmt who I believe have been treated for myasthenia gravis (MG) at Mayo Clinic, some of who have eye issues related to MG. They can share more about their experiences at Mayo.

I see in other comments that you have an upcoming appointment at Mayo Clinic later this month. That's fantastic. You're in good hands at Mayo Clinic.

As someone who has been dealing with ocular MG for several years and also living with ocular cicatricial pemphigoid, I'm sure that you have a list of concerns and questions for the experts at Mayo Clinic. What questions have you prepared? Which Mayo Clinic will you be going to: AZ, FL or MN?

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Replies to "Hi @wcburns2, I expanded the title of your discussion to reflect your question and included it..."

Could you describe some of your experience with ocular MG?

Thank you for tagging me. When I went to Mayo last month, I had several tests, with the main 1 being the ENG, and Myasthenia Gravis was ruled out. I was diagnosed with Parkinsonism. I do have several symptoms of PD, but they are very slight but seem to be increasing. So I will continue to see how I progress.