I don’t go anywhere these days without Mr. ALS. Not the grocery store. Not the swimming pool or locker room at the YMCA. Not even to the mailbox at the end of our driveway. Mr. ALS is like the awkward kid at summer camp who has yet to learn how to give it a rest.
Last week, Peggy and I traveled to Southern Arizona at the invitation of dear friends, to spend some time relaxing together, and to experience first hand the complicated issues of border security and immigration reform. More on those two thorny controversies in another post.
Air travel with Mr. ALS is a whole new adventure. No carry-on luggage. No sprinting for a just-in-time departure. New with this trip is a welcome ride in a wheelchair to the gate and between connecting flights. Oh, and lest we forget, once in flight, there is the long, unsteady walk down the long narrow aisle to the tiny bathroom with a folding door.
Even without turbulence, every person in every aisle-seat notices Mr. ALS. I nod and smile, imagining what they might say when Mr. ALS and I are sitting squarely in their lap.
And then, lucky for us, there is TSA. A supreme adventure unto itself.
Relinquish your cane. Remove your shoes without falling down. If you’ve decided to wear your AFO (brace for foot drop), it comes off too. Then we get to negotiate the slight incline into the scanner, which I’d never noticed before traveling with Mr. ALS. Once inside the scanner, we must help dear old Lefty raise a hand overhead, which requires a bit of gymnastics. Righty grabs hold of Lefty and hoists both overhead for the 5 seconds it takes to scan my insides. The exit off the incline is the last hurdle before finding a chair to reassemble the footwear. All of it deserving a round of applause.
In general, TSA agents seem mystified by Mr. ALS. I interpret their universal expression as doubt. I don’t often introduce Mr. ALS, which perhaps is rude of me, but based on their quizzicality, and everything else I need to do, so as not to fall down, I have chosen to let that opportunity pass by.
Last week, a TSA agent at a busy, metropolitan airport tainted the TSA adventure of with a fetid twist of meanness unseen before, beginning at her scanner. Peggy had already helped me to get un-shoed, with cane, shoes, backpack, and vest on the belt. (There are no chairs on the entry side of the scanner.) The TSA officer barked orders like a grim-faced Victorian school marm:
- “Step forward!” I shuffle forward over the lip, into the scanner.
- “Get into the scanner and put your feet in position,” pointing at the yellow footprints spread apart. I adjust my feet, carefully.
- “Raise your hands over your head.”
The agent’s bark must have rattled Righty, because there was no time for the usual gymnastics to help Lefty, who, upon command, barely made it shoulder high.
This is when the barking turned into shouting which felt like screaming.
“He can’t raise his arm,” she shouted, over and over, “He can’t raise his arm,” signaling to the other agents that assistance was needed.
Then, shouting at me, she continued her tirade: “Get out of the scanner.” “Move.” “Get back out of the scanner!”
Even as I shuffled out of her scanner, she continued to yell at me, now adding a humiliating shushing-wave of her hand. “Step aside. Stand to the side.” I quietly obeyed.
As the others behind me marched forward, I felt their sympathy. Notably, no one said a word.
I stood to the side with Peggy who steadied me until a tall, cheerful agent took charge. He spoke calmly, and quietly. He offered me his hand as I returned to the scanner. He smiled, and gently peppered his instructions with phrases like, “ You’re good, boss.” “Take your time boss.” “ Here, have a seat boss.” What a difference.
While Mr Smiles was assisting me, Ms. Barking Agent resumed her station at the scanner. Peggy was next in line!
I looked back in time to see Peggy lean into Ms. Agent’s face with a stern comment or two. While Peggy’s voice was low and forceful, Ms. Agent shrieked something incomprehensible.
“What did she say,” I asked as we re-united along the conveyor belt.
“I told her the shouting was uncalled for, that you had ALS, and that a little kindness would be helpful.”
“And she said…” I asked.
She said, “I don’t feel like being kind today!’”
This outlandish statement, and the behavior that preceded it, are examples of anti-kindness. They are unkind actions that prevent or inhibit kindness.
Once we recovered from the effects of anti-kindness, and recounted the practicle kindness of Mr. Smiles, Peggy and I wondered what might have motivated the anti-kindness in Ms. Agent.
- Maybe Ms. Agent eschews kindness, because she equates kindness with being sweet, and she perceives her job as being tart.
- Maybe Ms. Agent has never experienced kindness, and therefore has no reference for how to be kind.
- Maybe Ms. Agent is scared of making a mistake or being thought of as weak.
- Maybe Ms. Agent has learned to yell at people to get things done her way.
- Lost and broken wheelchairs.
- Refused boarding because you must present yourself in a wheelchair long before able bodied passengers, if you hope to have your wheelchair on the flight.
- No wheelchair waiting at the connecting gate, as promised
- Fellow passengers maligning someone who moves slowly or has slurred speech.
- Think about it. How does anyone with a wobbly gait or the inability to walk get to a toilet on an airplane?
- And, why do trains and subways, city buses, and even the trams between airport terminals have wheelchair and handicapped seating, while the entire airline industry has gotten away with not offering these accommodations?
Frankly, I don’t think it should be necessary for those of us traveling with a disability, like Mr. ALS, to announce and explain our unfortunate circumstance to merit a bit of practical kindness that affords us inclusion and participation in the ordinary inconvenience of present day travel.

Jim, your words not only convey the incredible challenges and obstacles that folks with varying abilities must contend with but also the fierceness of your partner and advocate Peggy, and maybe most importantly that undeniable grace you possess in meeting every day. We love you! T
My father had Bulbar Onset ALS and lost his ability to speak. His ears worked perfectly fine, but for some reason everyone spoke to him as if he was deaf or had a mental condition. That was when I realized that I needed to be a kinder person to those around me as they may have an invisible handicap that is none of my business. Prior to this personal experience I can recall seeing someone using a handicap spot and walk perfectly fine to the front doors of the store and I would likely judge them without cause which is truly unfair, and it takes seeing your loved one treated with such disrespect that you realize that you need to be part of the solution moving forward and spreading kindness.
Dr. Ogan,
I’m just reading this now. I am amazed at your patience and generosity with such anti-kindness and thank you for opening my eyes to the larger anti-kindness in the design and processes of air travel for the many among us living with disabilities. Amazing that you live this and have a sense of humor while recounting. My family misses you and we all send our love.
Dear Jim,
I’m always amused, moved, and inspired by your writing and your open sharing about what life is like with Mr. ALS. Today, I was really angry, too. Shame on that agent! The story reminds me to dig deeper every single hour of every single day to be kinder and more patient.
I’m glad to see you and Peg are getting around and having some fun – and meeting some big shots, too! BOB is a favorite 🙂 Happy Easter and Love from the Argons
Jim,
Your grace, patience, perseverance and kindness is a testament to your beautiful faith. Thank you for sharing!
Dr. Ogan,
This and the other stories and insights you have shared on this blog (and in your wonderful Medical Center Hour) are so beautifully genuine and teach us all how to be better humans. Thank you for all of this and for having taken such loving care of my children and nephew in your practice. We miss you and send our love.