When I was given the go-ahead to travel after my transplant, I was terrified. Buses, subways, and shared vehicles to get around town were nerve-wracking enough: I always wore a face mask, sometimes I wore gloves, and I never left home without a full complement of anti-bacterial spray, wipes, and hand sanitiser. I had been notified early on by the doctors that it was dangerous to board a plane and that I’d basically have to wear a hazmat suit if I did decide to do so. The first trip I made was to Miami, only six months after transplant. It was ambitious, but I felt at the time I had to do it.

I booked the ticket, but only after weeks of U.N.-worthy negotiations in my head and with my friends. And by ‘negotiations’, I mean flat-out freaking out. Family, friends, and the occasional stranger and I tensely pawed through the pros and cons: the risks involved, what might happen if I got sick in Florida, what the consequences would be if things went south, how I would manage the sleeping arrangements, what I would be able to eat—and so on. And the pros: the prospect of warm sand underneath my feet as I stood at the ocean’s edge, time with friends in a social setting—something I had very little of in those first months, and respite from January in New York City. 

Even in my imagination I was, at this point, too scared to consider dipping my bare toe in the ocean for fear of bacteria entering my system. My imagination, however, was also able to picture myself far outside of the four walls that seemed to be shrinking in on me during the many months I was stuck there, feeling lonely, sick and depressed. The four walls that defined my world were oppressive and safe, holding me tenderly and choking the life out of me. Three-and-a-half years later, the room is gone; my parents moved three floors down to a smaller apartment, with no lingering vibrations or memories to shoot out of nowhere and shock me into that grim state of dependence and dis-ease. Three-and-a-half years later, I can picture that room and feel gratitude and a general “Fuck You” attitude in equal parts.

At that time, I had only really been in the cocoon of the apartment, and I barely ventured out into the grime-filled city. I was still too afraid to eat in restaurants (bacteria), or even go to the park (rats). I certainly didn’t dare enter the subway (nor had I yet been permitted to by the doctors). I had acute symptoms of PTSD and I was not prepared for the big bad world. I was no longer the fearless girl let loose in India at 18, the supposedly well-seasoned traveler who got accidentally kidnapped and lived to tell the tale. Here was someone new: nerdy and delicate, who for months regarded a trip to Brooklyn as impossibly exotic, a faraway dream.

The apartment also oppressed my parents; my mother spent as much time in it as I did, often on her feet and making grilled cheese sandwiches I usually had to put down after a bite, making runs to the laundry, and changing the sweaty sheets. My father made me breakfast each morning which more often than not went barely eaten, and took regular trips down to a butcher on 9th Street to pick up bone broth and organic meat to make stews with: since I had to eat a certain amount of protein a day, I could no longer be a vegetarian. Everyone was tired. I was getting better, and I became aware of life beyond my self-contained world. Sometimes it’s easier to do the things we fear out of altruism, and to be able to give my parents a much-deserved rest after months of intensive care-giving appealed to me enough to start turning the tide. I also knew that if I didn’t venture out, our collective heads were likely to explode. In the end, my desire to do something to help ease the frazzled nerves of our family won out over fear, (added to that the ripe seduction of freedom - at long last, freedom!).

Yet the girl who, since the age of seven had filled two passports— American and British—with stamps and visas from four continents, must have been in there, somewhere. That girl left the dreary worrywart at the gate and boarded a plane heading out of subzero temperatures in New York City to land in warm and sunny Miami. I booked in a safe-sounding 6 days, so I could get back in time for blood work the following week and back to my sterile bedroom for safety. When my transplant PA gave me the green light to go, her only words of advice were “Don’t use the airplane toilet.” I couldn’t believe she let me go. I half-expected her to put the kibosh on it immediately when I asked (and half-hoped, since my fear needed something to feed on). But the angel let me go.

This first trip was rocky. There were tears in transit; there were tears pretty much daily. If you told me tears were healing waters that bathed my new liver, I’d tell you I was over-medicating. But there was lots of laughter, too, the famous ‘best medicine’, more powerful than tears, with highly preferable side effects. I had to laugh at my first plane trip. I was slung into a wheelchair and used the airport assistance in New York and on landing in Miami—which was an entirely new paradigm for me. I wore a mask and doused myself with hand sanitiser so often that I may as well have showered in the stuff. I used half a box of antibacterial wipes trying to scrub away germ-infested surfaces, which included every part of my seat. I imagined an invisible jelly of strangers’ dead skin cells, splattered, dried vomit, carelessly changed babies, the drool of passed-out drunkards. I didn’t even look at the toilet, much less go anywhere near it. When I was in-flight, I wrapped my scarf around my head so no germs could enter, or germ-infested people could come anywhere near my personal space (it was January after all). Anytime someone coughed, I flinched. I’d like to say that’s the only time I travelled in that way, but those rituals continued for a couple of years. That was the only trip I would make in that first year of transplant, because of a rejection episode that came in April. But it was a triumph. It spelled an idea of actual life being a possibility after transplant. I hadn’t been so sure.

The next trip wouldn’t be until the beginning of 2017, when I went to LA and was equally as terrified, but with a bigger bag and more trauma under my belt. I cried at least five times, coming and going. I broke down even before the plane took off because, weakened by two years of undernourishment and over-medication, I couldn’t lift my hand luggage high enough to go into the overhead bins and the flight attendant—bizarrely—refused to help me. It was a low moment and one in which I wished the devastation inside my body was visible, so I didn’t have to explain.

I later sent a strongly worded letter to the airline, which was far too verbose and a wee bit overwrought—but I saw clearly that the people on the flight who were supposed to help wouldn’t help me because I didn’t look like your standard “disabled” person. Even worse, I could practically see speech bubbles over their heads calling me spoiled, over-privileged or lazy. In response, they said they were taking the matter seriously and gave me $100 for my trouble, which made me feel a little cheap (and yes, of course I took it). I booked five flights with it. Ya, right.

I’ve often experienced this perceived ableism. People, strangers, to whom you appeal for help with heavy baggage, a place to sit down because of a dizzy spell or…fill in the blank…can be obtuse and unhelpful. There are various levels, from a look of subtle disbelief, to eye-rolling, resentful assistance. But the worst is when someone just dismisses my stated needs, which happened with more regularity as I recovered and now looked so good. I have tried to be stoic and ignore my own needs before asking for help. This is not advisable, but I’ve found it inevitable that even when I clearly state my medical history and explain real dangers to my immune system in a situation that poses no threat to anyone else, my careful explanation is not always met with compassion or even understanding. Sometimes it’s actually easier to navigate by practicing stoicism, rather than complain. And of course, sometimes you meet someone who gets it, and helps.

After the success and joy of venturing for the first time outside of my four walls, I’ve gone full throttle into travelling. I take precautions and take care of my transplant, and luckily, I’ve always been ok (touch wood). The very tired, very frightened person who couldn’t imagine putting even one little toe into the Atlantic Ocean in Miami has been slowly re-growing fins. I cautiously began to swim back to myself, starting with speedboats, canoes, even a sailboat; I went on to floating on a raft in a clean Canadian lake, I let white water whoosh over my feet in a Vermont creek, I dove into a certified-sanitary swimming pool.

On the two-year anniversary of my transplant, I stood with my feet in the sand looking out at the Cantabrian Sea—next to the Atlantic Ocean once more. I took a few ginger steps into the salty and warm August water, salty tears pouring out of my eyes. I cried not only because I finally found the courage (and opportunity) to swim in the sea but also because I couldn’t believe my growth—that I had emotionally overcome the fear that was so present for so long. And I could not have got there without self-work, therapy, and a commitment to reminding myself that I was transplanted to live, not to hide. And though I often do let fear take over—I still flinch if I’m sat near someone who displays even a slight sniffle (but I no longer make faces, which was always a bit rude), it’s not the first thing I reach for.

My doctor told me that the surgical masks don’t actually work very well against microbes in a plane, and that I only really had to wear one if it made me feel better. So I always travel with a supply of masks; I put one on if I feel I need to, but I’ve relaxed about that, too. I still douse myself in hand sanitiser and make sure I wipe down my arm rests and the back of the seat in front of me. I realised last year that, unconsciously or not, I trained myself to never touch my hands to my face in transit. I finally started using the toilet after my bladder was about to burst after a short trip to Canada last year, and now I just make sure to hose myself down on arrival. The shower is my first port of call. I think we should all take up this practice, considering how disgusting airplanes are. I don’t use a wheelchair anymore, but if I’m forced to stand for a long time, sometimes I rethink my decision. Standing for long periods of time result in dizziness and fatigue, and any unwanted attention I get sitting in a wheelchair beats the spectacle of me in a heap on the airport floor.

Ah, fatigue — that pesky foe. Travelling fatigues me completely, in a way it never did before, when a latte or a melatonin was all I needed to reset myself after a 15 hour flight (after which I could easily go out dancing for a further 15). Granted, I was younger then, and most people past their 20s are fatigued by travel. Since the transplant, it takes me a little longer to bounce back from jet-lag; the big difference is that now my body is overcome with an ache that seems to permeate every cell in my body. Knowing that this is my usual reaction, I make sure I am mindful and try not to push myself too hard—although it can be tough to resist going from baggage claim to a party. Last year, I took a chance on a trip to Colombia, and nothing bad happened (except for having all my credit card details stolen, which is less transplant-related and more idiot-related). There wasn’t a shred of ambivalence: I loved every single second. In 2015, I couldn’t have imagined taking such a trip; even in 2017 I probably would not have believed you if you told me it was a possibility.

We all have something that defined us pre-trauma, illness, or accident, and our greatest fear or challenge is that we might not be able to be/do that again. Growing up the way I did, travelling, speaking other languages, learning other cultures, meeting new people felt like some essential part of who I am. The fear of losing that great privilege was huge, but it was just one possible change among so many actual and potential upheavals. It’s not at all lost on me that my privilege is two-pronged: not only am I able-bodied enough to travel now, I also have the means to do it. Even though I’ve had to take certain precautions in the way I carry myself: from the street, to the airport terminal, to the bathroom, to the aircraft—it’s made me more mindful in general, and the small tweaks to my travel routine (what some might call quirks) are a small price to pay to be able to continue to experience the world. The big welcoming world that I’d almost lost.


When I was seven years old, my parents moved from New York to Hong Kong for my dad’s job, and we set off on an adventure that would change the course of this little Queens Chick’s life. Two years later, we moved to London. At the end of the school year, my teacher had me point to where my family was moving to on a world map and all the kids in my class “oohed” and “aahed”. My seven-year-old brain could barely fathom that a plane could travel that far, much less that there was life beyond New York. The farthest I had travelled by that time in my short life was to Boca Raton in Florida to visit my grandpa. It was the start of a grand adventure, of living all over the world, gathering people up as I went. As I got older, I would get the two year itch — to move on, to keep exploring, to discover new experiences and people. I ended up going to seven different schools and lived in six different countries by the age of 18. I was what they might call a precocious motherfucker. Even though I was always aware of my privilege, and knew it was really just good fortune to have had the opportunity to grow up in such a global way, I still took it for granted in many ways. I thought it would always be accessible. I wouldn't change my experience: I’m inordinately lucky to have lived in other countries at such a young age and see the world in an outward facing way, and to be comfortable living in other countries and cultures. But it can make you feel adrift and like you have no real home. That’s where the friends come in.

Most international school kids will tell you the same thing: once you find the group of friends in which you feel at home — you stick to them like glue, since the rest of your life experience has been so transient. The proverbial glue can mean lots of long-distance relationships over WhatsApp groups, FaceTime, Skype and thank-god-for-the-internet messaging. When you repeatedly show up as the new kid in school and then fall in love with the people around you, only to be forced to move on, you hold on to the good ones.  And try to create some semblance of community wherever you go. I used to sob for hours on end the night before going to a new school. I’d feel particularly different and weird for a while and then slip right into the fold (ah, the resiliency of children). I never felt like I fit in, anywhere, because I was not always only the new kid but also foreign. I am foreign wherever I go, which I’ve come to see as a great gift. I fit in with a group of freaks who understand that experience and have a similar conundrum of not actually having a straight answer to the question: “Where are you from?”. I’ve luckily found them, and because of that — many of them live in other cities, countries, continents. If you ask me where I'm from I will have to ask you how long you have and to please never ask me where I'm from. 

So when I got sick, and was dragging my feet on taking my sorry ass to the hospital, I’d call and text consistently with my multiple long-distance relationships (and also with those who did live near me and also with anyone who would listen, the guy at the bodega on the corner, the cleaning lady at work—the world needed to know and I was getting those phone numbers). Two of my good friends, Jenny and Mike, had just started dating and I acted as confidante to them both. It was basically me just telling them both to man up and fall in love (which they have, successfully — well done guys). My matchmaking services are available for a price as long as you keep a guest room for me wherever you happen to end up and feed me and maybe pay me a stipend. 

When I’d consult Mike about my symptoms (who is definitely not a doctor although I treated him like one during those early days), it would mostly go like this: 

“Mori, I don't know what to do, what should I do?” 

“Nora, you should seek medical help immediately.” 

Then I’d laugh it off and change the subject. I’d keep him up-to-date on the deepening yellow of my eyeballs or how many public bathrooms around NYC I managed to vomit in that day. Through out my subsequent recovery he maintained that healing crystals would not and could not save me. He may have been right, but it didn’t stop me from taking them with me wherever I went for protection. I no longer carry a heavy sack of crystals with me wherever I go, but I do carry one in my pocket and spread them all round my house. Jenny allowed me the space to sob down the phone to her later on, as did many, many-a-loved one —in person or virtually. I certainly upstaged their new relationship with my liver failure, but thankfully they didn’t hold it against me.

At the time we were also planning a trip to Central America for which we had a Whatsapp group called “7 wonders of world tour” (terrible name probably created by my friend Faris). The group provided endless jokes — including the below photo to indicate what I would most likely be doing on the trip. It wasn't too far off from what I would, in fact, be doing in the coming months.

I would send them (and the cleaning lady) photos of my yellowing skin and pock-marked face. I’d get separate messages back “You don’t look so good,” and “What’s going on?!”, and “What do the doctors say?!”.  No one quite knew how to respond and it was difficult to really convey what was happening over text message. Technology does have its limits when attempting to accurately convey a total breakdown of one of your vital organs. Hell, it was hard enough to see in person. Still others would provide comic relief in moments when I didn’t know how to react to the whole horrid thing. 

As time has gone on — it’s now been three years since first getting sick, and two years since my liver rejection — I don’t speak to everyone as much and I no longer ask for consults because I have a team of professionals to do that. Some of that is circumstance: lives get busier, kids are born, moves are made, time feels in shorter supply. But the idea of knowing my people are just down the other end of the phone is enough to get by on. There were times in my illness and recovery I could no longer speak to anyone, because I had nothing to say — and things felt so, so bleak. I’ve since dug myself out of that hole (with considerable help from family, friends, mental health professionals, my social worker, and spiritual teachers). It helps that I am now able to live more and be out in the world — which means I have more to talk about than I did for a long time. Sometimes it’s still hard to pick up the phone, but I push myself to connect when I’m able, because I know it’s how to participate in my community. My world is no longer limited to the merry-go-round of doctors appointments, medication and setbacks. It doesn’t feel so tiny anymore, and I don’t live in the confines my bedroom, shuffling from my room to the kitchen to the bathroom and back again. Although my reality does include the medical appointments, the medication and its accompanying side effects plus the prospect of an occasional setback — the limitations of my experience are less confined. I’m grateful for all the Facetiming I did in my darkest days, and for the many times I didn’t pick up because I just couldn’t face it and for my friends who still stuck with me—and kept trying. And for the knowledge that you can come back to yourself — changed, bruised but still breathing, and maybe for the better.