Diagnosed with Breast Cancer Just Months After Turning 40, Stephanie Cosby Advocates for Early Screening
Stephanie Cosby had her first mammogram at age 40 and was diagnosed with breast cancer. Two weeks later, her mother was diagnosed with late stage breast cancer. Stephanie shares her experience of breast cancer treatment and of caring for her mother, who has since passed away, here and in a blog she created to help other women dealing with breast cancer issues.
Stephanie Cosby calls herself the new "poster child" for getting a mammogram at age 40.
I’ve been a nurse for 10 years and used to work in a breast cancer screening
program, so I knew how important it is to get a screening
mammogram at age 40. Within days after my birthday, I’d scheduled
the appointment. During the exam, the mammogram tech told me that I’d
probably be called in again due to the density of my breasts.
When I returned for the follow up mammogram, they found a lump that no one
had been able to feel, including myself during my monthly self-breast exams.
A few days later I had a breast biopsy. I had to wait only 5 days (two of them
were weekend days), but when you are waiting for the news you may have cancer,
it can seem an eternity. On a Monday afternoon in August the radiologist called
me and told me I had breast
The crazy thing was I felt healthier than I’d ever felt in my life. The
lump could not be felt, the cancer was early stage and I had no signs and symptoms.
I felt like I was completely ready to take on this opponent and win. I looked
to the Internet for the most current types of treatment. Once I learned about
cutting edge treatments, I researched area Breast Cancer Centers. I chose the
Marlene and Stewart Greenebaum Cancer Center at the University of Maryland because
of the types of treatment that I thought I wanted to pursue. Even before my
first appointment with the Breast
Cancer team, I had questions prepared to ask members of the team. Like most
women, I was more interested in pursuing a lumpectomy with either chemo or radiation
and was very interested in learning if I was a candidate for the Mammo-site
During my multidisciplinary appointment, I met with the breast surgeon, the
breast cancer coordinator, medical oncology, radiation therapy and plastic surgery
teams. I peppered them each with many questions. I also met with a cancer center
volunteer who had battled breast cancer and won. It was very reassuring to hear
from someone who’d been there.
My breast surgeon outlined the options available to me and encouraged me take
a few days to really consider the right choice for me. The choices based on
my diagnosis were lumpectomy with radiation or mastectomy
alone. I was really leaning towards lumpectomy and radiation, but then a life-altering
event happened that would change everything. Fifteen days after I was diagnosed,
my mother was diagnosed with metastatic breast cancer. Within a few hours I
went from believing that I had no family history to having a mother and great-grandmother
with breast cancer and a great uncle who’d died from prostate cancer (which
can be genetically linked to the breast cancer gene.)
Armed with this new information, I met with a genetic
counselor from the breast program. She looked into my family history, talked
about my risk of recurrence and offered genetic testing for the breast cancer
genes BRCA-1 and BRCA-2. It was yet more information to help me make my treatment
I chose to undergo a bilateral mastectomy with reconstruction. When I met with
the plastic surgeon, he told me that he could use my own belly fat to reconstruct
my breasts. This was truly amazing to me. I wanted to have a treatment that
would allow me to continue through life not having to worry about recurrence.
My surgery last 14 hours; they told me this ahead of time, so it wasn’t
a surprise. The recovery period was about eight weeks. Outside of the usual side
effects of recovering from surgery (no heavy lifting, take it easy, look for
signs of infection), I experienced much less pain than I thought I’d have.
The breast cancer team was very supportive and available for any concern I had.
Best of all, I was declared cancer-free and had no need for any chemo, radiation,
or any other medication.
At the start of this journey, I was determined that cancer was not going to
change who I was or who I am. The hardest part of my experience was to focus on
my own healing while being concerned for my mother’s health. Sadly, she
had waited too long to seek care for symptoms she was having and she died three weeks
after my surgery. Walking the breast cancer path together, though, profoundly
changed my life. I feel that in some way her diagnosis saved my life. And the
Breast Cancer team at the University of Maryland had the treatments and technology
to make it so.
Since I experienced breast cancer from either end of the spectrum (my own early diagnosis and my mother's late one), I feel like I can tell women “don’t wait!” My outcome was the result of
very early detection. My mom’s outcome was the result of very late detection.
I have seen the face of breast cancer close up, at its worst. Being afraid of
a mammogram is natural; but if caught early, breast cancer is a curable cancer!
I’m not a breast cancer survivor. I’m not “surviving.”
I’m LIVING! In honor of my mom, I now live every day to the max.
For more information about the UMGCC
Breast Evaluation and Treatment Program, or any of our other treatment programs
or services, please call the cancer center at 1-800-888-8823.
This page was last updated: April 8, 2015