very close to me, taps on each of my arms, and asks me to tell him which arm he is tapping on. Then he does the same with each of my fingers on each hand. There is more neurological terminology chatter between them. I am starting to get annoyed. I look Dr. Volt straight in the eye and say, âYouâre going to explain all of this to me later, right?â He looks at me as if Iâve spoken out of turn. âWeâll talk about this at the end of the exam.â
He asks me to place my palm out flat, tells me that he will draw numbers on my palm with his finger.
âWhat number is this?â he asks.
âEight.â
âAnd this?â
âOne.â
âAnd this?â
âZero. Zero. And I think that oneâs zero too.â
They start to get excited. The three of us walk to the hallway outside, where Dr. Volt tells me to walk away from them, then toward them. Then on my heels, on my toes. I overhear Dr. Volt say to the resident âsee the duck walk, the stiffening of the gaitâ¦â I become self-conscious and loosen up at the knees. âThere, now itâs gone.â
Though theyâre trying to hide it from me, I can tell theyâre really getting worked up, and Iâm getting excited too, though I donât know why weâre all so excited. The tension mounts with each test; I feel like the quarterback on our little winning football team about to make the winning neurological touchdown; after I walk up and down the hall again weâll all high-five and throw the contents of the waiting-room water cooler over our heads. Instead, the end of the exam catches me by surprise. The resident leaves, and Dr. Volt takes me back to the room and tells me to talk to the receptionist about when to schedule my neuropsychological testing. I feel a bit let down, even a little used. I want to say, âGuys? Wait? Hey, guys? Do you want to, like, get coffee? Oh right, you already have coffee. I see.â
I try to stall Dr. Volt as he jots some final notes on my chart. âIâm used to leaving a doctorâs office with ⦠something. A diagnosis. Could you at least tell me what you saw? Did you ⦠gather any important information?â He looks up from his notes and laughs. âWell, we wonât really know anything until we get back your MRI and neuropsych testing. And maybe a PET scan ⦠Then weâll all meet to discuss the results.â I stare at him blankly. âHere, go home and Google this.â He writes something on his prescription pad, tears off the page, and hands it to me.
âBut I am often wrong,â he adds. âDonât hold me to it.â
On the slip of paper heâs written âGerstmannâs Syndrome.â I think, Oh good, I have a syndrome . A syndrome feels as if it grants me more purchase than a learning disability, although really itâs just a new name for the same set of symptoms.
*Â Â Â *Â Â Â *
I may have a rare neurological disorder, a mysterious condition, the main signifier of which is the inability to tell my pointer from my pinky.
What Is Gerstmannâs Syndrome?
Gerstmannâs syndrome is a neurological disorder ⦠characterized by four primary symptoms: a writing disability (agraphia or dysgraphia), a lack of understanding of the rules for calculation or arithmetic (acalculia or dyscalculia), an inability to distinguish right from left, and an inability to identify fingers (finger agnosia).
This is the first description that I find when I punch âDevelopmental Gerstmannâs Syndromeâ into Googleâs search field, translated from Dr. Voltâs scrawl. The definition is from the Web site for the National Institute of Neurological Disorders and Stroke.
Gerstmannâs has the feel of a hot-dog diagnosis, stitched from a pile of leftovers. Take a tube filled with bovine guts; where some see a hot dog, others see a cow. Both would be right.