Did anyone's diagnosis of primary, secondary, or tertiary AI take years?
I have secondary. I was on my death bed before I found out. Endocrinologist said I could of had it for a long time. Mine comes from my pituitary gland being scarred and too small
Primary: first symptoms presented in 2014, but I wasn't diagnosed until September of 2018. I saw specialist at multiple hospitals, but it took a desperate last ditch attempt with a little diabetes clinic to be diagnosed.
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