
My name is Fallon, but most people call me Ayden.
I was barely sixteen months old when my little sister was
born... too young to remember how I felt when my parents brought her home. But
my mom loves to tell me how excited I was to have a new little sister to play
with. Come time to breastfeed her, mom says I would run to my room, grab a baby
doll, and mimic her every move.
I can't say that I wanted to be a mother even then, but for
as far back as I can remember, I've known I wanted kids of my own some day. In
fact, I had my future all figured out by the time I was in middle school. I'd
graduate from high school, go to college (or become a hippy), and marry my
childhood sweetheart. We'd then have six kids and live in bliss.
Most of my dreams have come true. But the six kids part hasn't been nearly as easy to make reality.
At fourteen, I began experiencing severe migraines. After
numerous tests and hospitalizations we learned I had a lesion behind my right
eye. No one seemed to know what caused the lesion, or what we might expect from
it.
My neurologist put me on a regimen of different medications
in the hopes of easing the migraines and various other symptoms. Shortly after
we seemed to get a handle on those, we began to notice that my menstrual cycles
were becoming increasingly irregular. When my period came at all, I'd be in so
much pain, I couldn't move. So my mom dragged me back to the doctor.
My PAP-smear was abnormal. They thought I had uterine
cancer. Within days, I underwent my first surgery. We found out later that I
didn't have cancer, but the rest of my teen years were a blur of neurology
visits, gyno visits, migraines, irregular periods, and a slew of medications to
help with both.
At eighteen, I underwent my second surgery. This time, I had
a cyst the size of a softball on my ovary. At that point, my gynecologist
informed me that I had PCOS and cautioned that getting pregnant might be a
challenge. I didn't plan to have kids right then, so he put me on the
Depo-Provera shot to help ease the menstrual pain.
Two years later, my childhood sweetheart (SS) and I were
married. I stopped taking the Depo shot in preparation for the day we decided
we were ready. A year later, we decided it was time to start working on
bringing home Baby #1. We visited with a new gynecologist who reviewed my
history. After more tests, he diagnosed me with PID of unknown origin.
Even though the brain lesion was gone, the neurologist
refused to clear me for IVF because of the stroke risk, so they put me on Metformin
and Clomid.
After the first round, by some miracle, I became pregnant.
SS and I were over the moon, making plans. Our first baby
was growing in my belly and we were going to be the best parents ever.
A month later, I miscarried.
Our hearts were absolutely shattered.
They shattered again when, eight short days after my gynecologist
confirmed the miscarriage, my little sister gave birth to her second son. He
was three and a half months early and had very serious medical complications.
We spent months by his side at the hospital while he fought for his life.
At that point, my husband and I decided to take a break from
fertility treatment. I couldn't take any more heart break, not while my sister
and my sweet nephew needed me.
For the next four years, we devoted our time and energy to
helping my sister care for her tiny little miracle as he battled for his life. You
can read his story
here.
I went to college and then to grad school. I volunteered
faithfully.
My husband worked his way up the totem pole at work.
We never used protection, and we never became pregnant.
In late 2009, we decided we were ready to try fertility
treatment again. We researched everything we could about IVF, and were making
plans to visit a Reproductive Endocrinologist (RE) when I got sick.
The migraines were more intense than ever before, and they
wouldn't go away. For days on end, my head hurt nonstop. When I fell in the
living room one day, my husband had enough and dragged me to the emergency
room. They called the staff neurosurgeon to discuss my history, and he informed
them he wanted to see me first thing the next morning.
He was waiting for us when his clinic opened. By the time I
left his office two hours later, he'd scheduled me for a battery of tests he
wanted done before the week was out.
After a lumbar puncture and a MRI/MRV, he called me back
into his office to inform me they'd found another brain lesion, in the corpus
callosum this time. He warned me that they thought I might have Multiple
Sclerosis.
We spent days waiting for further test results. When they
came, we learned that I, thankfully, didn't have MS. But once again, they
didn't know why I got lesions like this, what to do to prevent another one from
forming, or what to expect in the future.
They had no choice but to treat me symptomatically. We had
to get the migraines under control before they caused me to have a stroke or
caused brain damage in and of themselves. And my life was being seriously
impacted by the other neuro issues.
I began an entirely new regimen of medications.
My heart broke all over again when my neurosurgeon told me the
risk for IVF was just too high for him to clear me. We'd had so much hope, and
suddenly it was gone.
On top of that, the side effects from the medications were
incredibly difficult to handle. I was so confused, I parked in the middle of
the road the first time I drove. My husband took my keys. I hallucinated the
strangest things. My nightmares were worse than ever. I had allergic reactions
left and right. I was depressed. Angry. Devastated.
I pulled away from my friends, unwilling to burden them with
my grief. And I did grieve. I felt like all the medication had killed the
person I was, and I didn't know how to get her back with my mind clouded with
drugs that wreaked havoc on my cognitive function.
I poured myself into writing, my books becoming the babies I
felt I wasn't allowed to have. I churned out completed manuscript after complete
manuscript, refusing to let the brain lesion and medication take writing from
me too. My family convinced me to seek publication.
When they wouldn't stop pushing, I reluctantly agreed. Three
months later, I had my first contract offer. Things started looking up.
My teenage cousin came to live with us for a while. I
focused on being her mom.
When she left and my heart broke all over again, I stood
facing that same dark hole I'd been wallowing in since falling ill. I hated
that I'd kept myself there for so long, so I began pulling myself out,
determined not to be the person that just gives up when things get tough.
I finished my graduate degree. I began working as a social
worker. I forged new friendships. Published two novels. We moved into our dream
home. I bought my dream car. We adopted a cat and a dog to join our little family. Took vacations when we
wanted.
We were in a good place after years of uncertainty.
And then my husband fell ill.
He had a horrible cough and began losing weight rapidly.
Despite my badgering, he refused to see a doctor. And then he started coughing
up blood. His doctor told him to go straight to the emergency room. When we got
there, they did an X-Ray, and then a parade of people entered the room, each
asking a thousand different questions.
Had he traveled out of the country? Been exposed to
asbestos? Done this? Been here? Traveled there?
No, no, no no, and no, we told them.
They told us they'd found a mass in his right lung.
My world tilted on its axis. I was terrified. I was angry. We'd
gotten to a good place finally, and suddenly, the rug was pulled from beneath
us. Worse, my best friend was sick and I couldn't help him as he underwent test
after test. His doctor began preparing us for the worst. And then it came.
Non-Hodgkin's lymphoma in his lung and the lymph nodes in
his chest.
We were discharged from the hospital in a cloud of fear just
a few short hours after his doctors delivered that diagnosis. There was nothing
they could do for him inpatient. He needed to see an oncologist and a
pulmonologist.
We waited for our appointments for both. And when we got
there, the world tilted again. The mass in his lung had doubled in size in two
weeks. There was no way this was lymphoma. Once again, they began preparing us
for the worse. Small cell lung cancer.
They sent us to see more specialists, who ordered more
tests. All the while, he continued to get worse. He couldn't walk more than a
few steps without gasping for air. He was pale all the time, gaunt. He barely
ate. In a matter of months, he'd lost seventy-five pounds.
His medical team grew to include eight different specialists
and his primary care doctor. While they debated what to do next, he became too
sick to stay home.
We rushed him to the ER and they admitted him for the second
time. His doctor decided to take him into the operating room the next day to
remove several pieces of the mass to figure out what it was, and to try to
prevent it from strangling the top of his lung. The mass covered the entire
upper portion of his lung, killing it little by little. If they didn't figure
out how to treat him soon, they weren't sure they'd be able to save his life.
He spent the next ten days in intensive care, slowly dying
while his team did everything they could to figure out what was wrong. Finally,
finally, they had a diagnosis. Pulmonary blastomycosis. A rare, severe fungal
infection not indigenous to this area of the United States.
They began treating him, but the medication caused a severe
allergic reaction. His doctor came in to talk to us, and told us they didn't
have another option. Without that medication, he would die. So, we agreed to
let him pump him full of various other medications to continue treatment. His
kidneys began failing. But the mass in his lung began to shrink, too.
We made the decision to continue treatment.
His kidney function began to increase. He stabilized. His
medical team slowly began to believe he'd survive this horrible infection.
He became well enough to come home with home health to
continue treatment. Two weeks later, he switched medications. His kidney
function returned to normal. He stopped losing weight, began eating more. The
cough disappeared, and so did the blood.
As I write this, it's been four months since we almost lost
him, and his health has continued to improve day by day. In less than a week,
we go in for a check up to find out where we go from here.
We've had a lot of time to talk in the last four months. A
lot of time to think, to evaluate, and to realize that we've walked through the
fire, and we've both come out the other side a little healthier, and a little
wiser.
We've also had a lot of time to discuss the future, and just
as it always has, our vision of our future involves children. We don't want to
keep waiting to bring our baby home, not when we both know intimately that the
future isn't guaranteed for any of us.
We're both doing better health wise. We've completed our
educations and settled into our careers. I will be 30 in 3 weeks and he is 33. Our home is ready for a baby. We're
financially stable. There's no reason to keep waiting for the perfect time
when, in reality, there is no such thing. We both know that intimately now,
too.
So we've committed to getting pregnant in 2014. After SS's
check up, we'll begin talking to an RE to evaluate our options. We both very
much want to be pregnant and experience the entire crazy, beautiful journey.
But if the risk is still deemed to be too great, we're prepared to begin the
adoption process.
I'll be sharing our journey to parenthood here, alongside
one of my oldest and dearest friends, Jayme, who is taking that same journey
herself. Our lives have taken us in different directions, but our hopes and
dreams and love for one another have never changed. And I can't think of anyone
I'd rather share this journey with than her. Infertility unites us, hope binds
us, and motherhood waits for both of us.
xoxo,
Ayden