Kandy Moreau
DOES TIME REALLY RUN OUT
If an October 2024 medical chart notes a six-year life expectancy, should one
accept that estimate as a conclusion?
Predictions may be useful to doctors, but they are still guestimates applied to a
persons whose lives may have never followed ordinary paths. Guestimates shall not apply.
In my case, going back about twenty years ago, what began as an uneventful
physical with my primary care physician became the first step in a long medical education I
never asked for.
At that visit, his primary concern was my weight, which did not surprise me, and was
the number one reason I postponed regular doctor visits. Any ailment I mentioned
somehow found its way back to that subject. I understand the health consequences of
weight, and I know how mine has affected me. However, I believed then and somewhat
believe now, that nobody ever died of a fat ass alone. Contributing factors of some sort
would surely have been present. I have also always believed that my body deserved a
closer look than a single explanation.
That closer look began after the visit, when my blood work raised a new concern.
In about a week, his nurse called to say he had referred me to a specialist
because my blood work showed elevated platelets—around 600, when 400 is considered
normal. It was not alarming, but it was worth looking into.
A few days later, I received a call from the Maine Center for Cancer.
I asked the caller to repeat herself because I felt like I was about to pass out.
She apologized and clarified that she was calling from the Maine Center for Cancer AND
Blood Disorders, and that the concern was my blood. Three days later, I met with a
hematologist, who put me on an oral chemotherapy medication to keep my platelets from
climbing. For the next several years, she monitored me as my platelets rose and fell like a
roller coaster. The diagnosis was thrombocytosis: not extraordinary, but something that
had to be managed. Time, it seemed, was aplenty.
I researched platelets—high counts, low counts, and everything I
could find. But because I had no other symptoms, felt well, and was young and fearless, I
did not dig deeply enough or ask enough questions to push my doctor toward further
action. Looking back, we were both too complacent.
After she left the practice, my new doctor ordered a bone marrow aspiration,
something that, truthfully, should have been done years earlier. The result: just like that, I
had myelodysplastic syndrome, or MDS—a group of rare blood cancers
in which bone marrow stem cells fail to mature, causing shortages of healthy blood cells.
Contributing factors can include age, exposure to certain chemicals—which did not apply
to me—or prior chemotherapy treatment, which did.
There are several types of MDS, but the specific category matters less here than
what the diagnosis forced me to confront. There WOULD be a “time limit” attached to my
future, but that limit would depend on several factors that neither the doctors nor I could
possibly predict. It will be a wait and see situation, which is so easy to say, but so hard to
manage.
When I search for answers, I research everything—sometimes to an absurd degree.
In my search for “Why me?” I began building a list of possibilities, even though the damage
has been done and nothing can change, but you never know. Answers to mysteries are
discovered every day!
A bone marrow aspiration can disclose diagnostic findings, including genetic
abnormalities. Mutations, in other words—information we may not always want but
sometimes cannot avoid.
My search for medical answers also connected to a lifelong search for identity.
I have been trying to understand who I am since I was old enough to know I was adopted
and what that meant. Over time, I uncovered a painful and complicated biological story.
Based on what I found, it appears likely that my biological parents were closely related.
Too close. That possibility raised difficult questions about genetics, inheritance, and what
may have been present in my body from the beginning.
To be clear, I am not claiming certainty; I am trying to make sense of patterns that
seem impossible to ignore. I do have genetic mutations, and it is hard for me not to wonder
whether my biological origins played a role.
Proving that would require years of research, money, and a level of institutional
interest that people like me rarely receive.
But in my mind, before my body even entered the world, it was already fighting.
Then life added trauma almost immediately.
I was born in December; a cold month in the Northeast, and according to the story I
later learned, my biological mother left me outside in a cold trash bin, near the back of the
hospital while she hitchhiked a ride to Portland. I was found, and she was
institutionalized, but damage had been done. Psychological damage for sure once I
became aware of the story, though I have always wondered just how much I took in as in
infant.
Less than a year later, I was adopted.
By the time I was two, my adoptive father was abusing me, and my adoptive mother
failed to protect me. That became the landscape of my childhood.
When my adoptive parents divorced in my early teens, freedom felt almost
unbelievable.
Eventually, I could sleep without waking at every creak of the floor.
Within a year, while babysitting for a neighbor, I was assaulted again.
That is the larger context behind my resistance to simple predictions.
I started life with complications, and they kept building.
The physical issues appeared much later, but I believe the trauma contributed to my
body in ways I may never be able to prove. Had none of the trauma happened, would the
chromosomal issues have mattered? No one can know, and that is the point.
A diagnosis may describe a disease, but it cannot fully measure the life that carries
it. I believe my history—genetic, medical, and traumatic—has shaped how I arrived here.
That does not make me predictable. It makes me complicated, and complexity does not fit
neatly into a life-expectancy note.
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Hi!
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I’m a professional commissioned artist, and I’d love to work with you to turn it into one, if you’re into the idea, of course! I think it would look absolutely stunning.
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Best,
Lauren
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Very well written, and deeply moving. This line toward the end: “A diagnosis may describe a disease, but it cannot fully measure the life that carries it” is extraordinary. It captures the truth that nothing can take the story out of a person; even when wounded, even when facing illness, circumstances never fully define who you are. May you defy every life‑expectancy note any doctor gives you, and have many, many more days ahead.
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Sad. Very well written, all the same. The angst and trauma have been very well brought out.
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