One year ago today, I received my cancer diagnosis. One year
ago today, this train changed its course forever. I heard the words too many
people hear. In that instant, at 20 years old, I was a young girl just trying
to maneuver college, and in that instant, I also became a
#FutureCancerSurvivor. I immediately joined a club no one ever thinks they will
be part of.
In that instant, and in the weeks
and months that followed, I didn’t know exactly what was going to happen. I
just knew it would feel like a long road ahead. I filed an incomplete for my
summer classes and cancelled the rest I was registered for in the fall. For the
first few weeks, it was as if it didn’t really sink in. I felt like I was in “production”
mode, like I was preparing to go to the newsroom on campus and write someone
else’s story.
I had
diagnostic surgery and a helluva recovery in July.
I had
surgery to implant a port in my chest for chemo in August.
I began
chemo shortly after.
I lost my
hair in September, the day before my 21st birthday.
And all this time I refused to identify as a cancer patient.
In October,
I became weak. The daily visits to the hospital and infusion center for chemo
treatments had replaced the part of my mind responsible for hunger and appetite
stimulation. I lost 15% of my body weight and
never spoke because I was too nauseas, leaving nothing but internal dialogue to
turn into depression the four hours I was awake each day. But no one would have
known. I had a life to live. I wanted to continue as a “healthy” young adult.
My family kept me going.
But the side effects multiplied. Moody.
Nauseas. Horrible appetite. Little verbal communication (we developed our own
sign language). Cold, then hot. Neuropathy. Off balance. Weak. Ringing in the
ears. No taste buds. Hypersensitivity to smell. Tired.
In November, I celebrated the end
of chemotherapy. I still had various appointments to check on the aftereffects
of chemo, most of which included trips to the pulmonologist for my least
favorite activity- lung function tests.
More side effects appeared without
an invitation. Nerve damage. Dry skin. Skin discolorations.
And then I received a phone call
mid-November, 2 days after my CT scan, with the words “no evidence of disease”
(commonly referred to as NED, and some of the most glorious letters a
cancer-goer could hear).
I was fortunate enough to gain my
sense of taste back, slowly eat more meals, and gain some healthy weight again.
My boyfriend and I drove to Kentucky in the following weeks and met his parents
halfway for a cozy and quick vacation weekend in the mountains. I was thankful
to be in a car headed somewhere different than the hospital.
I was also fortunate enough to taste
every last bite on Thanksgiving, and even fly up to Wisconsin after Christmas
to say hello to family and friends. Before then, my immediate family and I
spent Christmas in Georgia together for the first time in our new home since
moving here five years ago. It was a mixture of alternating happy and sad
feelings to be so far away from traditions you’ve known since the day we
arrived on Earth.
Since my return to the South after
the new year, I have reenrolled in my college classes, picked up two jobs,
started writing for the university newspaper (and even hired later as the new
managing editor), spent spring break in beautiful Savannah, finished the
semester with a 4.0, and took on a summer internship along with my summer
classes. Chris and I found some time to drive up to Wisconsin again this summer
to pick up his new car and celebrate his birthday while visiting our hometown.
All of this brings me to today, my
cancerversary. Since I can’t change anything about the past year, I am deciding
to be proactive about the years ahead for both myself and the people I
encounter each day. I will not ignore the day that changed my life forever. I
will continue to think about the good that has come from my cancer. I
appreciate every person in my life and the energy they radiate. I appreciate
each day in a way I never could have imagined before. I now know what it means
to be thankful for each day I’m given, and just how precious time really is. I don't think that's truly understandable unless you are faced with death.
In August, I will have my next
quarterly check-up with my oncologist, as well as the results of my genetic
testing done this summer.
I still worry the cancer will come
back. With such a rare cancer, consisting of less than 0.05% of all ovarian cancers,
there isn’t enough available research and information out there to be sure it’s
gone for good (not to mention the secondary cancers tied to young adult
survivors from chemo). I think that’s part of my future, but that won’t stop me
from anything. Even so, I will always have a little bit of cancer fear that I
didn’t have before this day last year- Fear that I wish I never had to feel.
Nonetheless, I stand here a year
later, humbled by the support I have received and the love I have felt from
both near and far. I am 100% a different woman than I was a year ago. Empathetic. Determined. Passionate. I am
extremely grateful to have a voice by being able to write these blog posts, and
even to share my story to the girl sitting next to me in class.
I mean it from the bottom of my
heart when I say I want to help other women (& men!) realize that not going
to the doctor to get screened isn’t going to prevent you from getting cancer.
No matter your opinion or position on health care, be grateful and act upon the
fact that you have the responsibility to go to a professional and take care of
your health – something not everyone gets to have. I encourage everyone I know
and meet to get their annual screening and checkup, even if it is with a
natural/holistic doctor or whatever you believe in. Listening to my body saved my life.
While I have worked so hard all of
my life to follow my dreams, and now as college graduation is right around the
corner, I now have a job I never could have imagined but am just as passionate
about: Cancer Advocate for every other #FutureCancerSurvivor. Funny how life
works. I know I will celebrate many more cancerversaries, and I hope one day
every person diagnosed will too.
Please subscribe to stay up-to-date on All Things Ab!
Take care of yourselves,
Abi
Congratulations Abi. Your outlook on life is inspiring.
ReplyDeleteAnnette D'Amico
Abi,your story is so inspiring. I'm a coworker of your mom & she shared your blog with me. I was so captivated by your strength. I lost my mom from cancer 11 yrs ago. I'm so glad to know you'll be out there advocating for folks who cannot. Your outlook of life is do bright. Your story brought tears to my eyes. May God bless you & I will keep you in my prayers.
ReplyDelete