The first time my mother went to the ER was in September. She'd woken up dizzy, couldn't keep breakfast down, and by mid-morning she couldn't remember if she'd taken her blood pressure medication. My sister drove her in. Four hours later they sent her home with a note that said "viral gastroenteritis." Push fluids. Rest. Call if it gets worse.
The second time was November. Same symptoms. Headache this time, plus a kind of fog she described as "like wading through wet towels." The doctor who saw her was different. He wrote "possible early-stage vestibular dysfunction, recommend ENT follow-up." Sent her home with meclizine.
The third time was a Tuesday in January. My father — he's 76, still drives, still sharp — called me at 6:40 in the morning and said, "Diane, something is wrong with your mother. She doesn't know what day it is." I drove the hour and forty minutes to their house and took her to the ER myself.
Different hospital this time. Bigger city. I sat in the room while they ran labs and I watched my mother try to tell the intake nurse her own birthday and get the year wrong.
I am a hospice social worker. I have spent seventeen years at the bedsides of dying people. I know what end-stage dementia looks like. I know what a TIA looks like. I know what dehydration and electrolyte imbalance look like.
What I was looking at that morning wasn't any of those things.
But I couldn't say what it was. And when the first attending physician came in and started down the same path as the other two — "looks like another viral presentation, we'll keep her for observation, get some fluids in her" — I felt something cold settle in my chest.
We were going to send her home with the same wrong answer for the third time.