Wow ... you are fortunate. Did you have PMR first?

I was diagnosed with PMR a long time ago. My rheumatologist still asks me about having symptoms of GCA. She says that she is "required" to ask me the questions.

I usually respond by asking her how would I know if I had GCA. I have the symptoms of GCA but I'm diagnosed with uveitis and trigeminal neuralgia. I'm glad someone can differentiate the symptoms.

I regularly see an ophthalmologist because uveitis causes visual disturbances and potentially vision loss. My ophthalmologist always reassures me that there is no evidence of GCA when he looks at my optic nerve. I have other eye problems but fortunately not GCA.
https://www.mayoclinic.org/diseases-conditions/uveitis/symptoms-causes/syc-20378734
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Trigeminal neuralgia caused such incredible facial pain that I couldn't speak for myself whenever I went to the emergency room. I felt that facial pain but attempting to speak only made it worse. I could only gesture with my thumb to respond yes or no when I was asked questions. My wife would respond and provide more details as needed when a doctor asked me why I couldn't talk.
https://www.mayoclinic.org/diseases-conditions/trigeminal-neuralgia/symptoms-causes/syc-20353344
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An ironic thing happened when my rheumatologist got approval for Actemra. Since I didn't have GCA as a diagnosis he needed to seek approval before I could try Actemra. My medical records were carefully reviewed and the recommendation was to treat me "as if" I had GCA. My rheumatologist was instructed to follow the guidelines for Actemra use for patients with GCA.