Tag Archives: Sarai Washington

Death and Debt

11 Saturday Jul 2020

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Sarai & Noah, November 2003. (Donald Earl Collins).

My post today will be short. Today marks a full decade since the Sunday morning my youngest brother Eri called me, waking me up with the news that my only sister Sarai had died overnight at Mount Vernon Hospital. It was due to complications from sickle cell anemia, the disease that denies the body sufficient oxygen for carrying out it functions, ever debilitating and ever more painful as one grows older with it, as anyone with the disease can attest. Too many blood transfusions, too many invasive procedures, not enough healing. Sarai Adar Washington, who did live, and did try her damnedest to live her life her way, died at 27 years young.

Yes, I love her, and miss her still. There isn’t a week that goes by where I don’t think about her and the life that she didn’t get to have, the life that she did live, and how my life was affected by her existing. It causes me, Sarai’s older brother — one 13-plus-years older than her when my mother gave birth to her, one at one point argued for abortion to save us and her the anguish of the disease — to let out the occasional tear or feel a sense of loss. I can only imagine how much deeper the loss is for my mom, of course, and for my three younger brothers, who truly grew up with her. My only solace today is that Sarai isn’t here to try to survive the pandemic, because she most surely would not have made it if she had contracted COVID-19.

On the other end is the week that reminds me of one of the worst best decisions I have ever made. To take out the first $2,625 of what would be over $41,000 in loans between July 1987 and October 1996. I paid out the principal of my loans at least three years ago. But Sallie Mae (and PHEAA and Marine Midland Bank before that) set the interest rates back when those rates were much higher. Eight percent on a series of loans taken out between 24 and 33 years ago would be incalculable to a 17-year-old in July 1987. But as a 50-year-old, it translates to debt peonage, more than double the actual loans themselves. Except that I know that one way or another, this debt will go away, if only because I will stop living this life, eventually.

The proverbial “they” say the only two constants in life are death and taxes. No, there are at least three constants — death, debt, and taxes. Maybe in my death I can finally see my sister again, and see my debt and taxes burn in the fiery pit in the event horizon of a black hole.

Aside

Finding A Memory, Knowing the Whole Truth

16 Thursday Jul 2015

Posted by in 1, Boy @ The Window, culture, Eclectic, Jimme, Marriage, Mount Vernon New York, My Father, New York City, Patriotism, Politics, Pop Culture, Youth

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From Cam Jansen Mysteries, a series of children's books about a girl with a photographic memory who would solve mysteries and take pictures in her mind of the clues, August 9, 2012. (http://appraisingpages.com).

From Cam Jansen Mysteries, a series of children’s books about a girl with a photographic memory who would solve mysteries and take pictures in her mind of the clues, August 9, 2012. (http://appraisingpages.com).

No one’s memories — even those whom are eidetic or whose memories can be near photographic — are perfect, especially over the long haul. As far as the scientific community knows, there are no exceptions. I include myself in that category. This despite having a memory cycle that has seldom let me down. Since August 8, 1974, there have been only a few gaps of any major significance. I might not be able to tell you exactly what I had for dinner on July 16, ’85, but my guess would include either chicken and dumplings or $5 spaghetti with meat sauce and frozen chopped broccoli, both courtesy of my shopping at C-Town in Pelham, New York almost every day (it was a welcome relief from the heat of sitting home at 616, anyway).

One area where my memory had let me down was parts of the summer of ’76, the bicentennial summer. I could vague remember being down in the city for some of the festivities that July 4th, followed by a long sleep on the free Metro-North ride that day, only to end up in New Haven, CT because my father had been drinking and sleeping on the train, too. I remembered my Mom buying a Polaroid and taking pictures of herself and us and her new furniture at 425 South Sixth at the beginning of the month.

And I remembered that this had occurred a couple of weeks later:

My first memories playing with a group of Black males in Mount Vernon, New York are all negative. When I was six in ’76, a group of preteens on the neighborhood playground near Nathan Hale Elementary on South 6th Avenue tried to force me into sucking one of their dicks, practically sticking it in my face to do so. I got away before being truly scarred for life.

But I knew that I couldn’t remember what occurred beyond that, not only for the rest of that day, but for the next three weeks afterward. It had bothered me for years that I couldn’t remember beyond the flash of images I did write down.

Even in writing Boy @ The Window (which thankfully wasn’t about my earliest years growing up), as much as I drilled down into my past, I couldn’t fully conjure the memory of this incident. And when I did try, I ended up inducing headaches.

It was the year after publishing my memoir that I realized my headaches weren’t just because I needed new pillows for my neck. I had a repressed memory, maybe even more than one. I didn’t try to find a way to un-repress the memory, though. I figured that if I concentrated on other memories from the spring and summer of ’76, it would manifest itself, one way or the other. The key was my Big Wheel, the only toy I truly loved growing up, and my first “girlfriend” in Diana, who moved away at the end of first grade. Those memories helped me conjure up the buried memories I needed to fill in the blanks.

Cecil Parker Elementary School (formerly Nathan Hale ES), Mount Vernon, NY, November 23, 2006. (Donald Earl Collins).

Cecil Parker Elementary School (formerly Nathan Hale ES), Mount Vernon, NY, November 23, 2006. (Donald Earl Collins).

Over the course of a couple of weeks between Thanksgiving and Christmas last year, I either had dreams or wide-awake flashbacks that filled in my blanks. I was in fact sexually assaulted, by a light-skinned thirteen or fourteen-year-old. With the help of two of his friends, he had gotten his penis in my mouth while I was being held down to the ground on the rain-soaked, asphalt, Nathan Hale playground. I only got away because his friends were laughing after I spit his penis out of my mouth, laughing so hard that they were no longer holding me down.

I did a bit of digging into July ’76. I already knew from my memories it had rained on a Tuesday or Wednesday the week after July 4th. Turns out on that Wednesday, July 14, a quarter-inch of rain fell on the New York City area, as there was thundershower activity and high winds that afternoon, with a high of 78°F. That, unfortunately, confirmed everything.

1976 Chevrolet Nova, Seattle, WA area (not the right color, but the right model), July 16, 2015. (http://youtube.com).

1976 Chevrolet Nova, Seattle, WA area (not the right color, but the right model), July 16, 2015. (http://youtube.com).

What I remembered next after was probably just as horrific. I didn’t tell my Mom about my incident for weeks, because I was supposed to stay home while she went to work at Mount Vernon Hospital that day. I did tell her, though, about three weeks later, on the first Saturday in August, as she and my father were arguing as usual. And, my Mom being my Mom, she didn’t believe me, leading to my first attempt at taking my own life. I ran out of 425 South Sixth, straight into the street, and waited to be run down by an older Black guy in a Chevy Nova (more on that at a later date).

But maybe what triggered these repressed memories in the first place was the trauma of losing my sister Sarai in July ’10. After all, that’s also the week I learned that one of my younger brothers had been raped by a short Black guy in his early twenties while pursuing his video game addiction via arcades at the age of nine. As traumatic as that revelation was, it was my Mom’s response that was the most chilling. “It serves you right. I told you to stay away from that man,” my Mom said in response.

Maybe it was too much for my Mom to hear on the same week as her only daughter’s death. Then again, from what I’ve come to remember now, finding out about any one of her children being abused was always too much for my Mom to bear. As for me, knowing the whole truth has made sleeping much easier, my dreams more peaceful, and my headaches all about stress and neck tension.

Aside

RIP Sister, Sarai Adar Washington (February 9, 1983-July 11, 2010)

11 Saturday Jul 2015

Posted by in 1, Boy @ The Window, Carnegie Mellon University, Christianity, culture, Eclectic, Mount Vernon High School, Mount Vernon New York, Pop Culture, race, Work, Youth

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Sarai Washington, circa 2003.

Sarai Washington, circa 2009.

It’s been five years since I received my brother Eri’s call telling me what I had known and dreaded would come for nearly thirty years. That my only sister Sarai had died from complications stemming from sickle-cell anemia.

As soon as I picked up the phone five years ago, I knew. Sarai had been in and out the hospital for months since she had returned to New York at the tail end of ’09. Before then, she had lived either on her own or with two of her high school friends in Huntsville, Alabama since ’05. The skin and bone bruises, the constant blood transfusions, the always-there pain of sickled red blood cells circulating through her body. The average life expectancy for anyone with the disease is thirty-three years. That I had Sarai in my life for 82 percent of that life expectancy was still a minor miracle in the midst of what to me seemed completely unnecessary pain.

We weren’t as close in her later years, though. I mean, Sarai saw me as a bit of a father-figure when she was growing up. I had thirteen years and six weeks on her, so that’s how it goes. Between the 616 fire and homelessness for her and my other younger siblings in ’95, though — not to mention puberty — Sarai no longer treated me as her hero. That was fine by me. I already had too many people in my life who thought of me as some sort of hero or saint.

I think, though, that my sister enjoyed not really having to think about her future, about not feeling the need to grow up, since, what would be the point, really? I thought that because she knew more about her disease than anyone, it was her responsibility to grow up and find the best care possible to manage her disease, to bring some meaning to her life. That’s where our closeness became less so. I have a way of expecting more out of people than most people are willing to expect of themselves.

Sarai & Noah, November 2003. (Donald Earl Collins).

Sarai & Noah, November 2003. (Donald Earl Collins).

When Sarai came to live with me and my wife Angelia in ’03, to help us out with our then newborn son Noah, it was obvious that my sister was doing little to take care of herself. When I finally confronted her about her poor diet and unwillingness to watch over her disease, Sarai yelled, “You’re not my father!,” right in front of Mazza Gallerie, on the DC-Chevy Chase border (we had gone to see The Matrix Revolutions, much more for her than for me). Of course she was right. But of course, I was right also.

Sarai decided the next day to pack up her stuff and move back home to 616 and Mount Vernon, “where no one told her what to do,” she wrote as part of her going away letter. She also said that I “don’t know anything about the streets” as yet another familial “Just because you have a Ph.D…” coup de grace. I thought, “If I didn’t know anything about the streets, you and the rest of the younger siblings would’ve gotten your asses kicked through the early ’90s.”

But I knew Sarai’s letter wasn’t about the streets. It was about her living her life the way she wanted, without me or anyone else telling her how to take care of herself. That’s why she went away to Alabama for nearly four years.

Luckily I did get to talk to her a couple of times after that. Though we weren’t close, I loved her, and I know she loved me. The sad truth was, though, Sarai never had enough time to take charge over her life, and I couldn’t make her take that precious little time.

My Sister’s Death, Four Years Later

11 Friday Jul 2014

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Sarai, Yonkers Apartment, Yonkers, NY, December 23, 1995. (Donald Earl Collins).

Sarai at 12, Yonkers Apartment, Yonkers, NY, December 23, 1995. (Donald Earl Collins).

My sister Sarai Adar Washington died on this date four years ago, Sunday morning, July 11, ’10. If she had lived, she would be 31 years, five months and two days today. I miss her, of course. I know she’s better off in the sweet by-and-by, that living with such a permanent, unyielding and relentless terminal disease like sickle-cell anemia wasn’t a real alternative in the intermediate run.

Screen shot 2014-07-11 at 9.45.51 AM

Still, I do wonder what life could’ve been like for Sarai if she hadn’t had to live with this dreadful genetic illness. Things like whether she had experienced the joys of sex and relationships, of falling in love and having a person with which to share her love and life. Or if Sarai would’ve gone on to college after high school, as there would’ve been a reason for her to do so, to keep living her life as fully as she could. Maybe, once she did decide to move out and live with a group of friends in Alabama, she would’ve stayed there working, dating, having the best of times on her own.

There’s really nothing more to say. Sarai’s gone, and though I wish we’d been closer in age and thus closer as brother and sister, and she’d been a healthy person, it was what it was. So, for one moment on this day, let me say, once again. Sarai, I love you, and miss you very much.

The Lazarus Woman

22 Thursday Aug 2013

Posted by in 1, Academia, Boy @ The Window, Carnegie Mellon University, culture, Eclectic, Mount Vernon New York, Pittsburgh, Politics, Pop Culture, race, Religion, Youth

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Barbara B. Lazarus, obituary picture, July 17, 2003. (http://cmu.edu).

Barbara B. Lazarus, obituary picture, July 17, 2003. (http://cmu.edu).

Now that my book’s been out for a couple of months (between two and four months, depending on the e-book platform, actually), I’ve found that my thoughts sometimes drift toward those that are no longer around to read it.

Not so much my family or nemeses, though. Sarai, my only sister, who died in July ’10, would likely have never read a word of Boy @ The Window — it would be too honest an assessment of life at 616 for her. My late idiot ex-stepfather Maurice Washington was already unhappy with my numerous posts about his borderline personality issues and constant psychological and physical abuse of me and family when I picked up the phone one day that same week my sister passed.

As for my former classmate Brandie Weston — to whom I’ve dedicated my memoir (actually, a co-dedication that includes my son) — maybe, if she had been well enough. My favorite teacher, the late Harold Meltzer, though, would’ve begun reading  Boy @ The Window five minutes after it had gone live on Amazon.com!

But of all of those folks who are no longer a part of this corporeal world (or who have gone into some state of seclusion from it), one other person stands out today. My dear friend and mentor from my Carnegie Mellon years (and the six years after I finished), Barbara Lazarus. I’ve discussed her here before, but not lately. Probably because I do tear up sometimes when thinking about her support of me specifically and her work at CMU in general. Barbara helped make my otherwise rough and dehumanizing experience at CMU manageable and even career-affirming.

As I wrote about Barbara for the memorial service at CMU in September ’03:

I want to communicate to you that I am in complete solidarity with everyone who attends the gathering at CMU on October 17.  For me, Barbara’s work was more than about women’s equity in the engineering and science fields.  She was about ensuring that all (regardless of gender or race, and regardless of the degree) who attempted the grand enterprise of competing for a degree actually made it through the process … Barbara was a dear friend and mentor who truly believed in me, even in spite of myself.  I loved her, and I will surely miss her, as I am sure you will also.

That only approximated how much she meant to me during and after my four years of doctoral success and failures at CMU. The months immediately before my advisor Joe Trotter and my committee approved my dissertation were the worst, as is well documented on this blog. Barbara convinced me to not become hot-headed and drop-out of the program with a completed first-draft of my dissertation under my belt. She also managed to keep me from requesting a change of advisors so close to the finish line. She did offer to “step in” as her duties as Associate Provost would’ve allowed, but warned me that this political solution would delay my graduation. My connection with Barbara kept me from meeting Trotter in one of CMU’s parking lots late at night wearing a ski mask and dark leather gloves!

She became my best reference professionally and otherwise after those dark days ended with the end of ’96. She read my articles and my first book before they went to print. We swapped stories about family and life and religion. We stayed in touch even after I moved to Silver Spring, Maryland in ’99. Barbara died on July 14, ’03, just sixteen days before my son Noah was born. It’s been a decade, a month and eight days since she passed, nearly as long as I actually knew Barbara (roughly between October ’92 and July ’03). Boy, I wish I could’ve shared my first photos of my son with her!

There were a few people like Barbara at CMU during those years. Susan McElroy (now at UT-Dallas), John Hinshaw (at least prior to my Spencer Fellowship), Carl Zimring (before the O.J. verdict), the Gants and the other Black doctoral students I’d met there (all fourteen of us) were my CMU lifeline beyond multiculturalism and Trotter tired sense of migration studies.

But Barbara Lazarus and I had a friendship that went well beyond academia and career, and went undamaged by petty jealousies or sudden bursts of outrage from jury verdicts. I’d been to her home, met her husband and her kids, learned something about her as a person, and in the process, managed to be my better self even in the worst of circumstances. That is being a good mentor, friend and person. I just hope that I was the same to her, and that Boy @ The Window proves to be the same to others.

Sarai, 30 Years Old Today

09 Saturday Feb 2013

Posted by in 1, Boy @ The Window, culture, Eclectic, Hebrew-Israelite, Marriage, Mount Vernon New York, Pop Culture, race, Youth

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Sarai (with Maurice) at 12 years old, Yonkers, NY, November 21, 1995. (Donald Earl Collins).

My sister Sarai (with Maurice) at 12 years old, Yonkers, NY, November 21, 1995. (Donald Earl Collins).

It’s another February 9, more than two and a half years since my sister Sarai Washington passed away from complications due to sickle-cell anemia at the age of twenty-seven. Today would mark her thirtieth birthday. But given how Sarai’s life began, given her disease and the average life expectancy of people with it, it’s just as well that she isn’t here to become thirty. Sarai would likely be in pain, with skin bruises and lesions, laying on a hospital bed, in the middle of yet another blood transfusion.

My sister’s life and death is a constant reminder to forgive. It especially reminds me that forgiveness for us simple, linear humans is a constant process. It’s one in which we overcome our own feelings with the determination to love and to seek wisdom and grace. That Sarai had to endure sickle-cell anemia for twenty-seven years, five months and two days — or 10,015 total days — could feel me with enough anger so that I’d spend the rest of my life in hatred and contempt.

Not so much toward God. Even in eighth grade, I knew enough to know that people often cause their own calamities, and yet choose to blame God for the perditious decisions they made. No, there was a time I blamed my Mom, from the time I learned that she was pregnant with Sarai and for years afterward. Why? Because I also knew about sickle cell anemia, how it was a genetic disorder, and how two people with the trait had a one-in-four chance of passing on the full-blown disease to one of their progeny. And I knew this because my Mom explained the basics of it to me when I was eight years old!

My mother worked at Mount Vernon Hospital, where they very well could’ve run a genetic test for the disease at the prenatal stage. Of course, that would’ve given my mother a rather difficult decision to make about my eventual sister’s viability. But then again, she knew before the birth of my other siblings Maurice and Yiscoc that my now deceased idiot stepfather also possessed the sickle-cell trait. That she didn’t have any of them tested was, well, lazy and shameful.

I could’ve easily blamed my now dead ex-stepfather Maurice. He was a walking disaster area, as everything he touched turned into crap. Maurice never did anything in his life that didn’t hurt someone at some point. He never once cared enough about Sarai (or any of his other kids, for that matter) to make sure they were born healthy and whole. Forget about what happened to them after they were born. Maurice’s only real interest was telling guys standing on corners about his latest sperm injection. He also liked to buy cigars after the women had to endure the pregnancy and labor, abandoned by him in all meaningful respects in the process.

And there’s the grudge I’ve held against myself. As I’ve said in Boy @ The Window and in various blog posts (including “Pregnant Pauses” from November ’12), I never wanted Sarai here in the first place. Not because I hated kids or her. I knew what her birth would mean, especially after a year in which we were without food at 616 one-third of the time and three weeks’ behind on rent every single month. With my mother’s hours cut at Mount Vernon Hospital, we were on the verge of going on welfare, and I’d been taught by my mom to hate that. We were about to become a racial cliché, living and breathing racial stereotypes, and that went against everything my mother and nearly two years of living as a Hebrew-Israelite had taught me.

So how do I forgive? It’s simple, really (well, maybe not so simple). Forgiveness for me is a WWJD (What Would Jesus Do?) moment. Jesus said on the cross, just before he died, “Forgive them, for they do not know what they do.” I realize that even when we think we know what we’re doing, we don’t really know — we’re not omniscient, after all. We’re never fully aware of the effects of our decisions and actions, of all the intricacies and long-term implications.

That’s why and how I forgave and forgive — my mom, Maurice and myself. It’s the one thing I can honestly say I learned from Sarai, especially today, on her thirtieth birthday.

Sarai’s Death, One Year Later

11 Monday Jul 2011

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Sarai Washington, February 9, 1983-July 11, 2010

This was the eulogy I wrote for my sister Sarai’s funeral 360 days ago:

“On Sunday, July 11, 2010, Ms. Sarai Ador Washington passed away at the age of twenty-seven from complications from sickle-cell anemia. It was the battle of Sarai’s life from the moment she was born. Yet Sarai fought that battle with dignity and a sense that her life was worth living. For those of us who knew her, and knew her well, most of the time, Sarai lived as if her disease didn’t exist, or at least, didn’t matter.

Even in those first few months after Sarai was born, she was obviously in trouble. She hardly gained any weight, all of her food had to be fortified with iron, and she only had “three strands of hair,” as our mother put it. It was more like a few dozen in three spots on Sarai’s scalp. She always needed help. Sarai was in and out of the hospital, in need of the occasional blood transfusion, and at times in excruciating pain. Between the disease and the hardships what we were going through as a family during the early years of her life, it’s amazing to know that Sarai managed to survive in the worst of those worst times.

Despite all of this, Sarai managed to grow up and eventually find herself. She almost immediately gained a love of music, whether it was listening to her mother’s singing of hymnals or her older brother Donald’s horrible rendition of Michael Jackson’s “Man In The Mirror.” She sang in choirs with her brothers Maurice and Yiscoc while growing up. Sarai attended Mount Vernon’s public schools, where she made friends along the way. Though delayed by her bouts with sickle-cell anemia, she eventually graduated from Mount Vernon High School, in 2003.

Later that year she spent some in Silver Spring, Maryland helping to care for her nephew, Noah Collins before returning to Mount Vernon. In 2005 Sarai moved to Huntsville, Alabama to live on her own for the first time. In addition to working for Western Corporation as a customer care professional, Sarai found her voice, making a whole new group of friends, touching others lives in the process. Sarai’s wonderful sense of humor and sense of kindness were assets that her friends in New York and Alabama truly appreciated.

When her disease became more difficult to manage, Sarai moved back to Mount Vernon in the spring of 2009 to live with our mother. Though her illness had gotten worse, she still had dreams for the future. She was hoping to go back to school to earn a cosmetology license.

Sarai’s sickle-cell anemia complications got worse, so bad that she had no choice but to quit her job. Although Sarai in her final months was not always feeling her best, she still found the time and energy to spend with her nephew, Roshad Washington. Despite it all, Sarai lived her life her way. Along the way, she enriched the lives of her family and her many friends.”

There isn’t much that I’d change about what I wrote last July, other than the two or three minor grammatical errors that I didn’t catch because I was working on less than five consecutive hours of sleep per night. But I do wish that I’d been able to do more for Sarai while she was alive. I think about her almost every day, wishing that she’d stayed with me in Silver Spring long enough to look into Howard University Hospital’s work on sickle cell anemia.

Mostly, I think about how I wish the quality of Sarai’s twenty-seven years, four months and two days had been better, that her parents had been better, that my life could’ve somehow made her’s better. It just wasn’t to be.