My
Story...
So many people have been asking my family and me “How
did this happen?”, “When did this all begin?”
“How did you discover it?” etc. Although
posting my story on a website is not my first choice of communication
for a personal issue such as this, I wanted to make sure that
I responded to so many people’s requests for a “background”
of the discovery of my sarcoma and my treatment and diagnosis
to date.
In November, 2004, I noticed that I began to get an increasing
number of stomach aches. I also noticed that I looked and always
felt “bloated”. During my annual gynecological
exam, my Dr. ordered an ultrasound which revealed that I had
a fibroid tumor; a very common condition that affects a majority
of women (it later turned out that what the radiologist believed
was a fibroid tumor was, in fact, my sarcoma. Although
I have been told over and over again that sarcoma is so rare
that “if you’re not looking for it, you won’t
find it”, I have since switched Dr’s. to make
myself feel more assured).
The symptoms continued and in mid-December I noticed that I
had a constant low-grade fever that would “spike”
once or twice a week to about 101-102 degrees. I would also
experience consistent night sweats and a pretty steady loss
of appetite. After a few visits to my general practitioner,
she agreed that it seemed like more than the flu and proceeded
to do a number of blood tests. These blood tests confirmed
that I indeed had an infection “somewhere” in my
body.
After a week of more ultrasounds, CT scans and MRI’s,
I was ordered to undergo surgery to remove a large tumor (about
15cm) in my abdomen. I had surgery at Mt. Sinai on December
30th. In order to remove as much of the cancer as possible,
the surgeon also removed part of my colon, my appendix, and
other tissue in the area. The surgeon did an excellent
job and removed all of the visible cancer from me. I was a great
patient (if I say so myself!) and made a very fast recovery
from the surgery. I was back running on the treadmill in less
than three weeks!
We all hoped that the surgery was the worst of it, but unfortunately,
the post-surgery diagnosis was very concerning. After
analyzing my tissue under a microscope, the doctors told my
family that I had a very high risk case of sarcoma. They
said that I still had microscopic cancer cells in me, and that
cancerous growths are very likely to occur again in the near
future (80% of sarcoma patients have a recurrence within three
years).
Knowing that I needed the best possible care, we obtained a
number of opinions from various doctors. After doing so,
we made our decision to work with Dr. Maki/Dr. Singer at Memorial
Sloan Kettering. Dr. Maki is one of the leading sarcoma
experts in the world and Dr. Singer is the leading Sarcoma surgeon
in the world. We are so fortunate to live in NY in that
Memorial Sloan Kettering is one of the best cancer hospitals
and one of only a handful of hospitals in the US with a Sarcoma
Center designed specifically to focus on this type of cancer.
Dr. Maki and his team recommended that rather than perform follow-up
treatment such as chemotherapy and radiation, it made most sense
to closely monitor me with quarterly CT scans to see if and
where the cancer comes back. The short answer for why
they did not recommend chemotherapy at the time was that since
all of the visible cancer was removed from me, they would have
no way of truly gauging the progress of the chemotherapy. ..
and why put someone through something as strenuous as chemotherapy
if it would be difficult to measure its success.
The next 7 months were a strange combination of “normal”
and “anything but normal”. My family and I
did a great job of living life to its fullest and trying to
forget the “looming” CT scanes every three months.
The good news was that I was feeling GREAT! I joked around
with the Dr’s, that with the exception of the diagnosis;
the surgery was the best thing to happen to me. I was
living with so many low-grade symptoms that I didn’t realize
could be erased when the tumor was gone. My stomach aches
completely went away, my digestion got a lot better and I even
stopped snoring (Dave was very happy about that)! Over
the course of my 34 years to date, I would say that the months
of February – August were the best in terms of my physical
abilities (I was fit and looking good!)
I was so confident that the cancer was not back that I scheduled
a “day of Jen” for my August 2nd CT scan.
I would get the CT scan in the morning and then have a day of
lunch with friends, massages, shopping etc….a day to celebrate
my health.
Unfortunately, August 2nd became a day in the Dr’s office
because the CT scan (and subsequent ultrasound) revealed that
I had a smaller (5cm) tumor in the same area as the original
one. The good news (I love how Dr’s find good news
in anything) was that it was a local recurrence, meaning the
cancer came back in a place that was operable.
After meeting with Dr. Maki and Dr. Singer who were disappointed,
but not surprised, they recommended that chemotherapy was indeed
their choice of treatment before surgery to remove the tumor.
Their rationale was that because they could now “see”
something in my abdomen, they would be able to closely monitor
how the tumor “reacts” to chemotherapy. The
plan going forward is to have anywhere from 2-6 cycles of chemotherapy
(each cycle consists of 3 days in the hospital and 2.5 weeks
“recovering”). I will be getting CT scans during
the chemotherapy so that the Dr’s can analyze how the
tumor is reacting to the chemotherapy. The Dr’s
are hoping that if the chemotherapy works on what they CAN see,
it will also work on the microscopic cells that they CAN NOT
see. At some point during this process I will have
surgery to remove the tumor.
Thank you for all of your love and support! We are so
fortunate to have such wonderful friends.