I arrived in Millbrook at 10:48 a.m. for the Mardi Gras parade. I parked at the Presbyterian church.

The first person to greet me was wearing a Carnevale mask and cape. They immediately informed me they were Episcopalians, then asked if I wanted a beer.

“But,” I replied, “it’s not even 11 o’clock in the morning.”

“The Lord doesn’t live by Earth Time,” came the response.

A cold aluminum can was placed into my hand. I was ushered into a parade vehicle by a Millbrook policeman. My chariot was a snazzy Pontiac convertible, driven by the preacher’s wife, Miss Judy.

I rode atop the vehicle, waving to the crowd like a dork. I could see the looks on people’s faces as I passed by. Most were thinking, “Who is this idiot?”

My driver was cheerfully shifting gears. Happy as a clam.

“Are you an Episcopalian, too?” I asked Miss Judy.

“I am today,” she said, gunning the engine. “Hold on tight.”

Millbrook, Alabama, has been throwing a Mardi Gras parade for 18 years. This celebration is no

small affair. This is the largest Mardi Gras celebration north of the coast. “Southern Living” wrote about this parade once and said, quote, “These people are nuts.”

Which might not be a direct quote. But I, for one, can assure you that the people who throw this party are, indeed, bat-dookie crazy.

The Revelers Mardi Gras krewe is made up of approximately 120 folks who are deeply committed to fun. Most of them are in costume. Many have flammable breath.

“We maintain several floats, and we throw, literally, thousands of Moonpies and beads,” said one woman. “You throw so many Moonpies your arms are sore the next day.”

So I was excited. Mainly, because this is only the second parade I’ve ever been in.

My first parade happened when I was 13. I was a member of—this is true—the pitchfork drill team. Our…

Homewood. Supercuts hair salon. The young woman cutting my hair goes by the name Shelby. She is as country as a collard, with an accent like Ribbon cane syrup.

She is 21. She is constantly laughing. She smiles a lot. All the customers here do the same whenever Shelby is around. This girl is Pollyanna.

I ask where Shelby’s originally from.

“Woodstock,” she says. “Not the one in New York. The one in Alabama.”

I would have never guessed.

I ask how she got started styling hair.

“Started cutting hair when I was 10 years old. My mama was a hairstylist, but she didn’t cut men’s hair, so Daddy would hand me the scissors and say, ‘You cut my hair, Shelbylane.’ That’s my real name, Shelbylane. My daddy wanted me to have a double first name like a Southern belle. Do you want me to trim the clumps of hair shooting straight out of your ears?”

“Please.”

While Shelbylane works steadily, I’m trying to imagine a world wherein a grown man would give a 10-year-old child surgically sharpened scissors

and allow the child to take a whack at his head.

“Your father trusted you a lot, to let you cut his hair when you were so little.”

She laughs. “Oh, Daddy believed in me so much. His confidence in me made me what I am. When I was a kid, I felt like I could do anything because of his faith in me. Do you want me to trim your unibrow, sir?”

“Please. Does your father live in Woodstock?”

“No, he passed away.”

“I’m sorry.”

“It’s okay. He died when I was 14. I’ve had time to deal with it. But I miss him real bad.”

I know all about daddies dying at young ages. I know all about missing daddies real bad.

“But I have a theory,” says Shelbylane, firing up her electric clippers. “If you lose your parent…

She has long red hair. Fair complexion. A high-school senior. Quiet. Mild mannered. When she speaks, her voice sounds like Locust Fork, Alabama.

Her name is Morgan. Seated beside her is Clarabelle, a black Labrador wearing a Service Dog Alabama vest.

Morgan has paralysis on the left side of her body; her left hand doesn’t work. She has frequent seizures, she is sensitive to light. She has diabetes. She has low vision, and is nearly blind in one eye. Her intestines are paralyzed, too, so digestion is an issue. A day in the life of Morgan is no walk on the beach.

Her health issues stem from a previous bout with encephalitis (brain swelling). The encephalitis complications should have killed her. But they didn’t.

“Took me six months to learn to walk again,” she said. “But I knew I could do it. I believed I could.”

She’s a tough cookie. Morgan practically grew up in Children’s hospital, in Birmingham. Her youth was nothing like the average American childhood. While most kids were busy playing in their

backyard sprinklers, eating Flinstone Push Ups, Morgan was in a hospital room, relearning how to walk.

Her mother remained at her bedside. When Morgan was too paralyzed to feed herself or hold her head upright, nurses did these things for her.

“My happiest childhood memories are at Children’s hospital. Those people love me.”

In her teenage years, things have gotten even tougher. What she misses most is her independence. When you deal with the medical trials Morgan deals with, you’re always under supervision. This gets old, fast.

“I couldn’t do anything on my own. Couldn’t even walk the school hallway without nurses hovering around me, waiting for me to have a seizure.”

Morgan wouldn’t sleep by herself, for fear a nighttime seizure would kill her. She wouldn’t eat by herself, for fear that she would choke. She couldn’t drink a bottle of water without…

It was a big day in Heaven. Maybe one the biggest. You didn’t know this. Neither did I.

After all, you and I were merely going about our day, here on earth. We were doing our thing. Walking around the planet. Driving our vehicles. Buying stuff we need. Visiting Publix. Taking kids to school. Cooking supper. Making important phone calls. Paying bills. Buying hemorrhoid cream. Whatever.

Meanwhile, something huge was happening On High. Something astronomical.

You see, our lives here on Earth are so small. Sure, I know it seems like you and I are the center of the Solar System, but we aren’t. Our lives, our schedules, our concerns, our problems, they are all so paltry in comparison to the Hereafter.

It all began this morning. Heaven’s big party was scheduled for 7 a.m. There were posters all over. Even posters plastered on the Mother-of-Pearl Gates.

Everyone was coming to this party. And I mean everyone. This was going to be a party with a capital P.

All week, the angels have been fluttering around,

getting everything just so. Saint Peter even booked a band. The band included the Duke Ellington Orchestra, Glenn Miller, Wolfgang Amadeus Mozart, Ludwig van Beethoven, Strauss, Debussy, and Hank Senior was on vocals.

There was an all-you-can eat buffet that was about the size of six U.S. states. One of the administrative angels ordered an ice sculpture that was about the size of Des Moines.

There were trillions—no—centillions of people who gathered. More people than you can imagine. So many people that, when you looked into the distance, the entire horizon was made of heads.

There was an electricity in the air you could feel. The clock was showing 6:58 a.m., Earth time. Everyone was ready.

Then, suddenly, the back of the crowd started going nuts. The roar was deafening. Not figuratively, but worse, metaphorically.

Because God was coming to the party.

God wasn’t…

“Hello. Thank you for calling customer service, website support,” says the woman’s voice, with a pronounced foreign accent. “How may I help you today?”

“Yeah, hi, I have an issue with my website. It’s not working.”

The sound of a keyboard tapping. “What seems to be the issue, sir?”

“My website. Like I said. It’s not working.”

“I see. And are you having a problem with your website, sir?”

“Yes, I just told you.”

“Describe this problem to me, please, in great detail?”

“Okay. None of my blog subscribers are receiving my blog post via email when I send the post out. Ergo, my website isn’t working.”

“Ergo?”

“That’s right. I think it’s a Latin word.”

“I don’t know this word, ‘ergo,’ sir. How do you spell it?”

“Does it really matter?”

“Will you hold please?”

“No, I will not hold. I was just on hold, waiting for forty-one minutes to talk to you, I don’t want to hold agai—”

Hold music.

Ten minutes pass.

“Hello,” says the foreign voice, “and thank you for your patience, sir, we are experiencing an unusually high call volume, but your call is important to us. What seems

to be the problem today?”

“I already told you what the problem was, remember? My blog post? It’s not going out via email?”

“I do not remember you, sir.”

“I was the one who used the Latin word.”

“Ah, yes. How can I help you?”

“I just told you, my blog isn’t working. None of my subscribers are receiving my blog post?”

Keyboard tapping. “Let me see what I can find out on my end, sir. Thank you for your patience.” More keyboard tapping. “Are you having a nice day?”

“Don’t make small talk with me. Please.”

“I’m sorry, sir? ‘Small talk?’”

“That’s right. I know you couldn’t care less how my day is going, so don’t pretend by making small talk.”

“What is this ‘small…

I arrive at the Shelby County Arts Council center. It’s early afternoon. I am here for the annual Helen Keller Art Show.

The parking lot is full of children. The kids are all dressed in their Sunday best. They are walking toward the building, accompanied by parents.

Several children hold white canes. Other kids use wheelchairs. Some are carried by their parents.

I see one blind young man run headfirst into a brick wall. He begins to cry. His mother holds him and begins crying alongside him. She is weepingly apologizing to her son for taking her attention off him.

“Hello,” says a tiny voice behind me.

“Hello.”

“My name’s Henrietta,” says the little girl. “What’s yours?”

Henrietta is using a pink wheelchair. A seatbelt is buckled around her tiny waist. Her face is cherubic. She wears a black and white dress with a jean jacket. Her eyes are looking past me.

“My name is Sean,” I say.

“Hello, Sean.”

“Is your art in the art show?”

“Oh, yes,” she says. “I won a Helen Keller award. I’m a winner.”

“Congratulations.”

“Thank you.”

Henrietta has

low vision. She can’t see well. Her eyes are just one of the many organs of her body with problems. Her physical issues stem from a mitochondrial disease.

The mitochondria are what turn sugar and oxygen into energy, so when your mitochondria don’t work, this affects different systems of your body: your brain, kidneys, muscles, heart, eyes, ears. Take your pick. A mitochondrial disease is not for wimps.

“I spend a lot of time in hospitals,” says Henrietta. “Sometimes, all I do is live in a hospital.”

The disease affects Henrietta’s immune system. Whenever Henrietta gets a common cold, it’s a big deal. When she gets the flu, it’s a national emergency; get her to the ICU.

“You must be a pretty fearless person,” I say.

“No way, I’m not fearless,” she says. “To be…