When I first meet Jefferson he is tucked inside blankets inside a cardboard box inside a tent inside a field hospital in Haiti. I am one of hundreds of people who have come to Haiti to provide medical care in the aftermath of a devastating earthquake. Our team has delivered a lot of babies, and we have seen and taken care of a lot of babies, so when I first meet Jefferson he is, to me, just another baby in a box.
I don’t know a lot about babies, and I’m generally not very good at being around babies, and I’m generally quite afraid of babies—and I joke, often, about how I might burst into flames if I have to be around children for any period of time, especially if said period of time involves the actual holding of babies—but this baby, this little baby named Jefferson changes me, and with his help I learn some very simple things: how to feed him, how to change his diapers, how to hold him. And he teaches me other things—the kinds of things I feel I have waited a lifetime to learn—about life, love, survival, death, tenderness and openness. He unlocked something, something deep, and there is some newness to me now.
For a while, at least for a few days, I don’t know his actual name, or at least no one tells me his name, which is okay because I typically call him Pumpkin. Jefferson feels tiny in my adult hands, and he is just one week old—born one week after the earthquake—and he has patches of dark hair on his head with a smidge of darkness for eyebrows and little bean sprouts of hair here and there. His parents brought him to our field hospital because he was sick, very sick, and so we have his tiny body in a make-shift baby warmer attached to wires and cords.
• • • •
Our field hospital is pretty awesome and fairly similar to what I saw when I watched re-runs of MASH when I was a kid. But our hospital is a bit rudimentary in that we don’t have all the shiny tools we would have in the States. By that I mean we lack pediatric ventilators, IV warmers, baby warmers, x-ray machines and various other things. Sean Penn, however, would later arrange for us to get a digital x-ray machine, which would arrive with pediatric ventilators—and a few hundred people would smile from a few thousand miles away.
While we lack equipment, we don’t lack creativity, and we have some amazing thinkers on our team. We don’t have much of anything for babies so we have to get creative. We MacGyver things together using whatever we have on hand: knives, duct tape, string, water bottles, syringes, cardboard boxes and plastic containers. We make baby warmers, pediatric breathing masks, pediatric feeding gizmos, containers for needles, and a hodgepodge of other things.
Carol is a trauma surgeon, and she is the doctor who is responsible for Jefferson when he is first brought to our hospital. She has gray hair, is an avid reader, and has a spirit and attitude that comes with age and wisdom—the kind of spirit and attitude that I craved when I was in my 20s, and am still trying to find now that I’ve breached my 40s.
When I wake up, sometime around four o’clock in the afternoon, I find my way to where we have boxes of MREs and rifle through them looking for whatever sounds remotely good—this does not include and will not ever include “beef patty” or “imitation pork ribs.” I also hoard empty boxes for Carol, because she likes to use them as baby boxes for the many babies we would see throughout the night.
In the ICU, with the help of whoever is on staff, we fashion them into baby boxes as needed. We stuff them with paper gowns and blue chux and silver emergency blankets that crinkle and irritate my ears with each touch. The actual box is not that large, but it is wide enough and deep enough and long enough to tuck a baby inside with blankets. We take the warmers that we would use to heat our MREs and tape them inside the box to keep the babies warm, or we take one liter bags of IV solution, hang them just outside the exhaust on the generator until they turn a gross brown, but they are warm and we have piecemealed together a pretty awesome baby warmer.
• • • •
Jefferson has neonate tetanus, most likely contracted from his umbilical cord in a non-sterile delivery. The prognosis for someone with neonate tetanus isn’t good. When I find my way to the ICU on this particular evening, Julie asks me to check on the baby in the box. Julie is a pediatric nurse with curly hair and an infectiously inspiring personality. She has one of those hearts, the ones that are surely made of gold, and if you give her a baby blanket and a set of sutures, she’ll whip together the best baby hat ever.
He is tucked inside one of our make-shift baby warmers, the silver emergency blanket covering his tiny frame. I pull back the top layer, find another layer, pass my hand beyond the warmed bag of IV solution and touch his little body. His temp feels good, feels warm, and he doesn’t move when I touch him, not even in the slightest. He has diapers on, and they are too big for him, and this makes me smile a little. I check the pulse oximeter taped to his toe, check his heart rate, his oxygen levels, cover him back up, this little baby in a box, and tell Julie that everything is good.
Jefferson sleeps in his baby box just one bed away from another patient with tetanus, a boy of about 16 who had to have his foot amputated when he was brought to our hospital in very bad shape: his jaw locked, his body mostly unresponsive. Not a single doctor on this deployment—and we have some awesome doctors with amazing backgrounds who work at major hospitals in major cities—has seen a patient with tetanus. Not ever. Here, in the same room, two beds apart, we have two: one tiny baby and one young man, both of who will be with us for many days.

I spend a lot of time in the ICU touching patients, calling the kids “pumpkin” and talking to them even though they are unconscious. I massage their arms, hold their hands and rub the tips of my fingers across their cheeks. And sometimes, when I am close to tears, I place the palm of my hand over their heart and say quiet words inside my head.
At night we meet for a team meeting and start the process of shift change and transferring care to the oncoming crew. We listen to everyone talk, listen to each Team Leader talk about things that are going on, and our lead doctor talks to us about Jefferson, about how we don’t have what we need to keep him alive, that this is how things go, that we need to say goodbye and that’s all there is to say about that. So we walk into the ICU—me and Julie and Carol and a handful of other folks—and we prep for shift change, and Julie sits with Jefferson and cries. I watch her from where I stand, and watching her cry while she holds his tiny frame breaks my heart.
I stand, two beds away from where I can see Julie crying, and I watch the kid with tetanus purposefully moving his hand, so I reach out to him, reach for his hand, and he grabs my hand and holds it in the way that guys shake hands. I try to hold his hand normally, the way one would shake someone’s hand, but he grabs it the other way. He hangs on tight, and when I pull my hand back, pull it toward me in release, he grabs my hand tighter and he does this every time I try to let go. He keeps me there for minutes, and I can feel tears are about to fall and I hold them back, tightly, and I hold his hand tighter and look at Julie and all the people in the room and it seems crazy and fucked up and wrong in so many ways.
Steph is one of the mental health professionals on our team. She has blond hair always pulled back in a pony tail, and she has a sense of humor like no one I have ever met before. Later, she would send email reminding us of how it is totally appropriate to run out of your tent in your skivvies after an earthquake as long as you have your helmet in hand. Steph walks up to me while I’m holding this kids hand, trying to let go and not being able to let go, and she touches me gently on the arm and asks if I’m okay. I can’t answer her. I don’t know how to answer her. I do know that if I say even one word to her I’m going to lose it, and I’m going to start crying in some endless sort of way, and I can’t do this, not here, not now, not in front of the 15 people standing in this room. But the tears come, slowly, and a few people notice this and hold my arm until I have to walk away and take a few deep breaths.
Julie pulls Jefferson out of the box, and she holds him and kisses him and several of us throughout the course of the night say goodbye to him. We hold him, this little bundle of goodness, and we don’t let go of him, not for even a second. Later, when things have slowed in the ICU and someone else is holding Jefferson, Julie decides he needs a hat, so she takes a baby blanket, measures his head, cuts a pattern and sews him a hat using sutures. She even makes the hat have a brim with a tassel on the top. This is, in my opinion, the best hat ever, but Julie will surprise me later and make an ever better hat, one with little ears on it, and this is the hat Jefferson would go home in, the one he would wear on his tiny head while his mother carried him out of our hospital while we all stood around and clapped.
• • • •
Jim has speckles of gray in his shaggy hair and is one of the three-person mental health team that is with us on this journey. He is also a chaplain, and he can play guitar, and he manages to get his hands on a guitar while we’re in Haiti. He goes around to the various tents and sings with the kids, and eventually he starts a bit of a band with some of the family members who have come to see their kids. Jim and Julie sit outside the ICU and they hold Jefferson and talk and cry. I wander outside occasionally, not wanting to disturb their moment. Jim holds Jefferson close, tight like a football, and at some point I ask if I can hold Jefferson. I don’t hold newborns much, almost never have, and there is a quick moment of learning how to hold the body and the head and transfer this little package between large adult hands. I hold this tiny body in my hands and snuggle him close and whisper things into his ear and after awhile I hand him back to Jim who stays up all night and holds him.
Jefferson has what we call agonal breathing, which means it’s a bit gasping. He doesn’t breathe normally, not in any sense of what we would call normal. He breathes slowly, and with random gasping breathes, and not for a single moment in 12 hours does any one release him from their hands. Morning comes and he is still breathing, still hanging in there, and we transfer him to the day shift, and they hold him, too, never let him go without touch.
Later, after sleep, I wake up and find that Jefferson is still here. That he is eating and thriving and fighting for his life. I ask the nurse who has been watching him if I can hold him for a while, take him for a walk, and she hands him to me and asks me to promise that I will feed him. She has been feeding him pedialyte through a syringe, and I take the syringe with me, with its oddly blue colored liquid inside, and I walk Jefferson to the main area where everyone eats and gathers between shift change.
Julie is sitting there, and she smiles when she sees me walk up with Jefferson. I tell her that he is eating and if she wants to hold him again she has to promise to feed him, because I have to uphold the promise I made earlier about making sure he eats. She looks at me and thinks quickly inside her head and asks me to get her some things: a binkie, a butterfly IV, and a syringe. She takes the binkie, which has a tube running from it to a syringe, and she sticks this in Jefferson’s mouth, and he starts to suck and eat and this amazes all of us. We watch him eat and get tired and fall back asleep. Then he wakes up and does it all over again—and this delights us to no end.

Deb is a pediatric doctor, probably in her late 40s. I have dinner with her one night, and she tells me she is eating better than she has ever eaten, all the while we tear open our MREs. It’s dark out, and I’m sure she can’t see the shocked look on my face, but I ask questions about her eating habits and learn a great deal of information. Deb talks to us and tells us not to get our hopes up, not to have hope that Jefferson is going to live. But she fits him with a feeding tube—a tiny tube that goes through his nose, down his throat and into his stomach—and we feed him this way. We put a syringe on the other end of the tube and squeeze formula and pedialyte into his tiny belly.
The next day everything is different. I wake from sleeping, eat my MRE, and then find my way to Jefferson. He has developed a fever over night and this is not a good thing. He is, once again, put on death watch, which is to say this is the second time—and there will be a third time. At some point we take out his feeding tube and wait for him to go—never letting him go outside the reach of human hands—yet he doesn’t go. There is some point, some marker, at which I’m quite sure Jefferson says “fuck you!” This is the point, I think, when he starts talking. By “talking” I mean he starts crying and getting fidgety and lets us know that he is fully aware of everything that is going on.
Christine is one of the mental health people on this deployment. She is the epitome of zen and has one of those styles and attitudes that silently whispers “calm” and being around her I can’t help but be anything other than calm. She is also one of the people who refuses to put Jefferson down, and if I want to know where to find Jefferson—so I can get a little J-Time—I look for her or a handful of other people who can be seen holding him close. She has a firm belief: that the reason Jefferson continues to thrive and do well is because of touch, because we have refused to let him die in a box, sit in a box, sleep in a box—because we refuse to let him experience anything but love and touch.
• • • •
Joan is tall, and whenever I look at her I think about passing her a ball so she can make the next slam dunk. She has an affection for Jefferson that goes deep, and she holds him as much as possible, and watches over him with an insanely endearing quality. When I see the two of them together she is like the mother bear protecting a cub.
I’m not sure what day it is when I wake up and stumble to the MREs, and I’m not sure how many days Jefferson has been with us at this point, but I take notes in my journal and comment on how he continues to thrive each day, on how he continues to prove us wrong. At this point he is a solid structure, the center of various hearts, and the center of a very large circle. Joan comes to find me and asks if I’ve heard about Jefferson’s latest milestone. Before she even tells me what this is, I burst into a huge grin and I think: “This kid rocks all that I have ever known.” At this point, Jefferson is nursing and he has had his first breast milk-related poop, and this is a pretty huge milestone for a kid we had put on death watch some three times now.
For the next day or two, I try to spend as much time as possible holding Jefferson. And I walk up to people like Carol or Christine or Steph and ask them if they need a little J Time, because we are all thrilled that Jefferson is doing so well that he can go home and be with his family. And there is a lot of holding and transferring of his tiny frame, and he cries each time he is shifted, each time there is movement so as to say “People! Quit moving me around! I need to sleeeeeep now!” I watch his brow furl, and his nose tighten and his mouth open, at which point his tongue does this rattlesnake type movement. And once he’s changed hands, he falls quickly back to sleep.
• • • •
On the last day that our team would spend in Haiti—another team had been deployed to replace us—we find out that Jefferson is going home. This gives us closure, the kind of closure you need once you’ve become attached to someone in some way you didn’t know you were capable of becoming attached. I spend the day knowing that he is leaving, and I ignore the whole notion of him leaving all the while I spend minute after minute giving him Eskimo kisses. Soon, Joan comes to announce that Jefferson’s mother has arrived, that she is here to take her precious cargo home, and we all run to the front end of our hospital where we can say goodbye.
We line up, some dozen or more of us, along the walkway just outside of our triage area. When Jefferson’s Mom walks up with him in her arms there is an insane amount of applause and tears being held back. She looks, I might say, not quite like she understands why we are clapping. And she walks past us, slowly, through the gate with a little boy who changed a lot of people.
When I get home, back to the States, there is a clear lack of Jefferson in my life. And every moment that he crosses my world—and this is a lot of moments, an infinite amount of moments—I say outloud: Hi Pumpkin!