Three Sections from MY LIFE

I received a long-awaited phone call from my social worker. But before I answered the phone I had one of those knowing-feelings and knew it would be the adoption agency telling me about my soon-to-be child.

Then on a crisp morning in Seoul, Korea, a wide-eyed baby was readied to leave his homeland. Dressed in a pink bunting to keep out the winter chill, one-year-old Kook Yung was carried aboard Korean Airlines, and he set off for a new life; adoption in the United States.

When the plane landed in California, Kook Yung was placed in my arms, and I felt awareness deeper than the ocean, grasping the loss his first mother endured. That boy became my son, Jay. The one who would later pick purple and yellow wild flowers for me, and bestowed me with the title of adoptive parent and the pleasure of being his mother. 

.   .   .

We had three kids. First I gave birth to our daughter and our son was placed with us as a one-year old with special needs from Korea. Then we added a third child to our family who came to us from foster care at age ten. When we decided to add more children to our family we wanted to make a difference in this life by parenting children who were already born, waiting, and needing a family. We wanted kids that were considered hard to place because deep down inside I knew adopting children who were waiting to be matched with parents was my calling in life. When I shared this with my husband he said, “I've got that same feeling.” Then we tortured ourselves by examining and delving into the myriads of types of special needs placements we wanted to pursue. We wanted a child with a special need, but we only wanted to take a small risk.

Looking back, I can see that our thinking was pretty much the same as those who claim they only want to parent a “healthy child.” We wanted to believe that it was possible to be in control of the outcome. We wanted to chart our future and to be able to map out our children’s medical conditions. But when I gave birth to my first child we were open to receiving our baby in whatever form he or she was delivered into this world with. Why then when it came to foster care or adoption did we insist on only children who would carry a medical label that felt minor and easy for us to handle?

Today if I were to bring another child into my family, I'd like to believe I would welcome the opportunity to consider all types of special needs, instead of only those requiring corrective surgery. Now I’d consider receiving a child with a host of unknowns, because the unexpected special medical need our son developed much later on, that we did not choose, which we would have given anything to avoid, has reshaped me, chiseled off my rough edges and softened me, made me better, and filled me with tender grace. But back then I was looking for a guarantee that my children would have only minor health issues.

After nearly a year of waiting, finally the call came and we received a referral for a one-year-old boy in Korea who was born with Syndactyly. His fingers on both hands were joined together, bones and all, making his hands look like small mittens. Might this child be right for our family? We wanted this child and we began to do medical research to familiarize ourselves with what this condition would mean. While we considered what might be ahead health-wise for our child to be, our good friend, Bruce, who is blind and lost his eyesight as a young adult, yet went on to become an outstanding wood craftsman and cabinet maker, kept telling us he had a strong feeling this was going to be one of those things we looked back on as no big deal, and that our little boy was going to be fine.

And when my son was placed in my arms, immediately I understood something was far beyond ordinary about him. He was calm and centered in a way that let you know he possessed a great amount of wisdom; his presence made skeptics believe in angels. 

There was something extraordinary about the trauma that surrounded Jay’s early life and how he eased his way through it. He endured the first syndactyly-release surgery when he was eighteen months old, and the process involved skin grafting, with grafts taken from the soft skin near his groin area. Every few months he underwent another surgery to separate another finger, and by the time he was five, he had ten individual fingers. Granted they were misshapen and scared. But he had fingers. Fingers that he could now stuff into gloves, or a baseball mitt, which delighted him, and he found his own way of making his new fingers work perfectly for his needs.

Turned out Bruce was right. The condition that caused Jay to be placed with us as “Special Needs” when we adopted him, turned out to be hugely unimportant. We’d managed to have an easy outcome, just like we set out to do in the beginning. It breaks my heart, however, knowing that if my son had congenital heart disease, or a host of other diagnosis, or if I had looked into my crystal ball, chances are we would have been frightened off, and might not have adopted him, causing me to miss out on having him for my son and some of the best years of my life as a mother.

The truth is before we adopted Jay I did look into my crystal ball, or rather I went to the hilltop and I got real quiet, and what I knew for certain was that if we adopted this baby, it would be wonderful, better than anything I could ever imagine, and that his life circle would be small. Within a slip of a moment I could feel my joy and pain braided together, and I knew that I was meant to take this journey. When I know something, I know. But how could I know? As a young child I discovered that often I feel things, and I know.

With my vision tucked into the recesses of my mind, for the next six years I enjoyed a blissful, wonderful motherhood, joyous beyond measure. Then suddenly ours life changed forever. I learned that 7-year-old Jay had a brain tumor. 

Following surgery, radiation, and then chemo, the cancer went into remission and the brain tumor was gone, and stayed gone for much longer than the doctors had initially predicted. Each time Jay had an MRI, the scan came back perfectly clear. He was back to snorkeling at the beach, and he looked healthy, if fragile. And on the head of a pin we delighted in eight more wonderful years, joyous beyond measure. And then the tumor came back, and Jay died at age 15.

Following my son's death, I felt the way Mt. St. Helens looked ten years after her summit was removed by a volcanic eruption. I stood under an evening sky watching the slate blue dusk blend into ragged peaks and lava domes. 

A friend once had a cabin perched on a bluff overlooking the lake, surrounded by gigantic pines, and now fireweed and purple-red flowers dotted the level earthen floor, in a place where a forest once stood. My son Jay, a pole star of my life, had passed. I knew I would never get over it. Nor would I ever be the same. And I would not give up or given in to societies mistaken notion of getting over grief. I’d find a way to learn to live with it and not allow it to hold me back. 

I walked, circling the crater, and saw wild violets blooming. The mountain had been scattered and sundered into bits, and she survived. I swallow a clotty grief deep inside my throat. A grief so wide it gives me laryngitis. Bold and enthusiastic thoughts of my son Jay filled me. 

I shuffled out into the empty field of my mind to find enough words to make it through another winter of writing. My life has changed into something I didn’t want, and I began gathering the pieces that were left of me, coaxing them back into growth, and starting again, but like the mountain I’d lost all of my big trees. 

I felt myself a part of the mountain, with hills catching the sunset through a furious wind, dust devils kicking up dirt. All my senses became alive, out on the edge. I imagined fireweed blooming on the burned over land in my heart with tiny purple petals, and it was a beginning.

That was in 1999. Like a river stone tumbling in the raging water, my grief has grown softer, and I found gold along the way, but I had to reach for it. If I had the chance to do it over again, I would choose to be Jay’s mother and take this journey again. Everyday I thank my lucky stars. Out of this has come an unimagined gift. Loving Jay with all my heart and soul, and having to let go, gives me the faith to open my arms and embrace each moment. The special need Jay came to this earth with—was to spread his love wide.

Race, Ethnicity and My Face

As a mixed-blood woman of Cherokee, Lenape, Seneca, and German descent, I came of age understanding that I'm not totally a Native person, and I’m not a white person. I'm a border woman dwelling between the boundaries. 

I have light skin, light enough that some people think I’m white. My dad, a Native man, and my mother, a white woman, had me when they were teenagers in 1953. 

I grew up in Compton, California. The family next door was Bolivian and they loved me like a daughter. My best friend was Japanese and Mexican. Still, when I was 10 years-old, my dad sat me down to have “the talk” with me about race. He told me about how to navigate the streets, about how to stay safe. He also wanted to make sure I understood that in order to be accepted by certain white people it mattered who your friends were. 

By that point, however, I already knew. 

I had discovered that when I went to the houses of my white friends after school I needed to be aware of how I was holding myself at all times. I learned to stay alert and watch for clues: sometimes there might be an older brother who pulled his eyes in an upward slant and said something mean about Chinese people; or a father that casually spouted racial slurs at people of color, and made fun of Indians. When this happened, I knew I had to make an excuse to go home and I’d never go back. Sometimes I’d make up stories when asked about my darker skinned, mixed-race family in order to protect them. But if the mothers of my white friends didn’t feel satisfied with my answers, I wouldn’t be allowed to stay at their houses for long. 

Things would be different when I went over to the houses of my friends of color. Their mothers would always take me in without hesitation. And if there was a grandmother at home who spoke English with an accent, or didn’t speak English at all I could usually be certain they wouldn’t ask me if my daddy had a job. In their homes, I felt safe. 

As a child I had things all figured out. But when I reached my late teens and early twenties it became more complicated. 

Hanging out with my friends of color meant witnessing them get treated poorly and face multiple instances of discrimination by white people. Being out with my white friends, however, meant that we could expect to be given preferential treatment no matter where we went. When I began dating and went out with Native boys or other boys of color in my community, I was considered “white trash” by many white Americans. I could even expect to have a white man point to my date and ask me what I thought I was doing being with the likes of someone like him. But when I dated the first guy that was white, I was allowed to be white by association and had access to the privileges of white America because of that. In stores or restaurants, we were always served or seated first, before people of color. 

When we acted up or got into mischief in public, it was laughed off as opposed to being taken seriously with the assumption that we were up to no good like it is for teens of color. My early adulthood was charged with decisions to make: Should I mention my Native identity? Should I let white people I don’t know well and may not ever want to become close friends with, assume I’m white? Keep my racial identity private from employers and others who would discriminate against me if they knew I’m a mixed-blood Native American woman.With dark skinned family members and dark skin friends, and with strong ties to Native America and firmly rooted within a community of color. 

When people look at my face, what they also can not see is that my mother, who was born white, is a member of a mixed-race family, with white and Black and Mexican family members. 

At age twenty-three, I found myself employed full-time in a company that was predominantly white. So white, that my intuition told me if my boss had known I was anything other than white, I would have probably not been hired. My white co-workers seemed to only accept people of color who adhered to white social norms and didn’t challenge their biases. They could not accept how vastly different the culture values, thought processes, and social norms of ethnic people were from white America. 

I wear the face of a woman with light skin privilege. While keenly aware of the advantage it has given me over my friends and family who are not able to pass, I always make the decision to disclose my Native identity. I never try to pass. Passing would mean turning my back on my Native family, my family and friends of color, and my community and my identity. 

Following my experiences working in a predominantly-white company at 23, I began to make sure that at each interview I had for a new job, I’d take a “racial temperature check” to ensure that people of color who looked like my friends and family were always welcomed. And I’d proudly list all the positions I’ve held within American Indian and Asian-American organizations on my resume. 

Later on in my life, I married a man who was white and we had a daughter together, before adopting two Korean children. Two of our kids had apparent ethnic features and their black hair and darker skin often caused people to mistakenly assume they were Native American. I knew that blending into white society would never be an option for them. So it was always a toss on whether they would be able to ride on the wings of my white privilege, or be subject to the racism that ruled America when they were out on their own. 

In turn, I did my best to connect them with their Korean roots by becoming deeply involved with the Korean community in our town. For more than four decades my heart and my soul was shaped by my connection to the Korean community for which I am grateful to be a part of. 

Now, in my 70s, my gray hair and wrinkled face reveal the many years I have lived. Yet what has not changed is what most cannot see: I am a border woman. Borders are set up to define or to separate, but I am neither part white, nor part Native. My blood is a mix between two worlds, Native and white merging together to form a third: a mixed-blood dwelling between the boundaries. 

First published in Santa Clara Review, vol 108 / issue 01. 

Copyright © Terra Trevor. All rights reserved.