Three days later the biopsy
results came back. No cancer! Deep sigh of relief for me and for us. Also, no Valley Fever. That was ok too, but that had never really
worried me. They were proceeding as if
this was just a large yeast infection. However,
the second doctor did not believe the pathology of the biopsies. He swore it was cancer and scheduled me for a
second esophageal endoscope four days after the first one so he could re-biopsy
the mass himself. My first thought was
that he wanted it to be
cancer. It made me mad actually, but I
went ahead and had it done again. After
the scope, he said he’d biopsied deeper and did well over ten different places
on the mass. I was still mad. I kept asking myself why he wanted this to be
cancer so badly. All I could come up
with was he either wanted the surgical fee, or he was one of these that could
not stand to be wrong. Probably both. The damn biopsies came back clear so LEAVE
it! But he didn’t. This round of results would be back in three
or four business days. Yay... I get to fret about it all weekend since it
was a Friday.
The following Wednesday we get a
call to come into the doctor’s office.
The biopsy came back as cancer this time. It was exceptionally small and it took two different
pathologists to see it, so it was VERY early on. So early and so small in fact that they
couldn’t differentiate the kind of cancer it was. He said the mass that I had was caused by the
Barrett’s Esophagus. What Barrett’s
Esophagus? No one ever said anything
about that before. I’d never had
symptoms, let alone a diagnosis that would have caused a mass that large. How can that be? We never really got a good answer for
that. The bottom line was it was
cancerous and we had to decide what to do about it. He was going to confer with the oncologist
and see what would be the best next step and would be in touch. While that was going on I was going to have
an esophageal ultrasound and a CT Scan to see how deep the cancer was and
determine what stage it was. The
oncologists said that it was so small and early on they would be surprised if
it was any more than stage 2. Try to
have a good Christmas… Gee thanks and
Merry Christmas to you too, doc.
The week after Christmas I had
the next scope of the esophagus with the ultrasound the CT Scan. Again, another three to seven days wait for
results. The results came back showing
it was NOT in the esophageal wall at all or behind it. This is good.
Another sign the stage was very early.
They set it as stage 1. This
particular type of cancer is rare and it is even rarer to find it this
early. I should consider myself
lucky. Sure, I’m lucky. I’ve got cancer. I’m real lucky. I was still in denial I guess. Next up, a PET scan to show if the cancer was
anyplace else other than in the esophagus.
The PET scan was done just after
New Year’s in January, 2013. By this
time I was getting numb to a lot. I was
not really hearing anything anymore. All
I knew was I had cancer. It was burned
into my brain. Very little else
registered. Not even the fact I was
still losing weight and not eating much.
The PET showed a bright spot exactly where the doc said I had the
cancer. That was expected. However, it
also showed that three lymph nodes also were glowing a little meaning that they
had cancer in them too. My brain did register that. Lymph nodes filter
the blood. That means there is a chance
that things could get worse. Great. We need to schedule surgery soon. This surgery will consist of taking out a
good portion of the esophagus as well as the top portion of the stomach, then
stretching the stomach up into the chest and re-attaching it to what was left
of the esophagus. Then he asked if I had
had any heart tests done. I never
had. Even though I had high blood
pressure, my heart health was never brought into question. My cholesterol was good and I did not have
diabetes, even though I was overweight.
He scheduled me for a heart stress test for the day before surgery to
make sure my heart could handle a surgery of this magnitude. Now I start to worry if I have the strength
to make it through the surgery, let alone the cancer. This just keeps getting better and better.
I'll see you all again in a couple of days for the next entry... Thanks for reading along!
Brian - Hope you gave that "stubborn" second doctor a huge hug when you realised what a great job he'd done by being so persistent. I know of a few examples where such tenacity was sadly lacking.
ReplyDeleteGlenn
Glenn... not a hug, but I did shake his hand and apologize for my attitude. He accepted the apology graciously and understood my stance and thinking at the time. I thank god for him and his crew every day!
DeleteI agree about the tenacity comment as well. And the fact that there are a lot of people have the same mindset that I had, "It read negative so let it be!" It's definitely a double edged sword.
Your path sounds almost identical to ours. Very very early is a good thing, believe you-me!
ReplyDeleteMajorly big time, Karen!
DeleteI'm just glade the doctor did double triple and quadruple check it could have been worse if he didn't find it. I'm glad he did even though it made u mad love u daddy
DeleteI'm glad to Lauren! I'd like to stick run a few more decades for you guys, and the boys and lea Ann and the entire family! And I love you too!
DeleteSo glad that doctor did push more test...Nino my husband had a hard time finding a gastrologist in our local area so I pushed him to go to our local VA who had one...he closed his practice to work at the VA ...this doctor also did my colonoscopy a few days before he did Ninos endoscopy .. he was going to come out to give me my results after Nino's test..well mine was put on hold as he came out and straight forward told me after doing so many of these test he was positive Nino had cancer but we will wait on biopsy report and told me to start searching where we wanted Nino to be treated for cancer. Nino was so out of it he really did not "hear" what the doctor said, I was in total shock and started researching right away. Nino was more "it is what it is" and did not want to research until I read enough to find out how important everyone said to find a specialist. The best part is you had a doctor who cared enough to double check. You have been given the chance to deal with it now sooner then later and share your story with us!
ReplyDeleteAbsolutely! It helps to have an up front doctor. :) and as to not hearing things and being out of it... I can 100% relate to that! I have been able to do that even when NOT under anesthetic!
DeleteI am so glad you had a tenacious doctor. I believe GI's are the weakest link of this whole disease. I don't think ours relayed the sense of urgency of Barrets or Gerd and I can tell you his recommendation of getting a scope every three years did not cut it. After my husband's scope that ultimately identified he had cancer, the dr. Opined about how he was getting his first scope and how he was checking for Barrets and was worried about it. He never relayed this worry about my husbands condition in the four years he had Barrets. I hope he has learned his lesson but I doubt it. It seems GI's run scope shops and that's it. Thank you for letting me vent, I have been holding on to this for a long time. N
ReplyDeleteActually my surgeon was cardio-thoracic, not a GI doc. I think that made a big difference.
DeleteAnd always feel free to vent! That is what these things are for. For me in the posts and you all in the comments!
Delete