Friday was my scheduled biopsy. Except someone failed to tell the doctor. I’ll explain.
If you have been following this in my other posts, then you remember that after I had an ultrasound, and they found a nodule, my doctor told me I needed to have a biopsy. This is to check for cancer. She referred me and sent my file to an ear, nose, and throat (ENT) doctor, Dr. S., in town. I called and specifically told the receptionist that I needed a biopsy. She told me they had received my file, and they were going to fit me in right away for the biopsy, since I had a nodule. My sister, Mara took off work, so she could accompany me to the doctor, and the boys’ grandmother graciously babysat.
We arrived at the doctor’s office and I filled out all the paperwork. Then we went back to the exam room, and waited for the doctor. When he arrived, he started going over my medical history. He asked me a lot of questions about my health in general. Then he pulled out a booklet and started explaining what the thyroid does, and what having a nodule means. I had a hard time focusing because I was wondering when he was going to start the biopsy.
He told me in my case, a biopsy is needed, but an ultrasound-guided biopsy at the hospital will give me the most accurate results. It hit me that I was not going to have a biopsy on Friday. About that time Mara asked if he was going to do the biopsy. He said he could do one with the needle in his office, but without the ultrasound, the results might not be very accurate.
I really wanted to get this done and over with already. I was tempted to tell him to just do it. But, no matter what the results were, I would have that question in the back of my mind- could I trust the results? I decided since I have to have it done anyway, I might as well make sure it is the most accurate it can be. So that means scheduling it at the hospital for the ultrasound led biopsy.
As we left the office, I was really annoyed and mad. I couldn’t believe the doctor’s office failed to tell me this was a consult only. I was also annoyed because now this means more waiting. I just want to get this behind me, one way or another. I tried calling the hospital all afternoon on Friday, to get the biopsy scheduled, but no one ever answered the phone! I was beyond frustrated. I can’t control it though, so I will have to just go with the flow.
The only silver lining, was I got a lot of my questions answered. The doctor told me after the biopsy, I should have results within 3-5 days. He also told me if there is cancer, they remove the entire thyroid. He says it isn’t worth the risk to just cut out the cancerous portion- the entire thyroid is removed. So I would be facing surgery. Then I would be on medication for the rest of my life. He actually increased the percentage of cases where it is cancer- to 15%. I had been told 10% previously.
Dr. S. told me if the nodule is benign, then I can decide to just leave it, but they would watch it very closely to make sure it didn’t become cancerous, which I can only assume more biopsies. He said sometimes patients decide to just have the benign part cut out, so they don’t have to worry about it becoming cancerous. That would mean surgery. He said they would still monitor the thyroid, but not as much. He said even when the biopsy shows the nodule is benign, and a patient opts to have the benign part removed, they will examine the nodule, and sometimes still find traces of cancer. He said if that happened, they would remove the thyroid at that point too.
I don’t like the way most of these options end. It sounds like nothing is for certain- even if the biopsy shows the nodule is benign- cancer could still be a possibility at some point. This information is preparing me for the choice I will soon have to make. Dr. S. told me my ultrasound showed some abnormalities, but he couldn’t make a diagnosis from just the ultrasound. He also said when the nodule measures more than 3 centimeters, they become very concerned. He said my nodule measured 1.7 centimeters. For some reason that sounded reassuring- like I don’t have this awful mass on my thyroid growing.
Dr. S. told me his own wife had thyroid cancer two years ago. She had asked him to be his surgeon, and he said she was fine today. He said thyroid cancer is very treatable, and is very slow growing. He told me it is the slowest growing cancer, and if I had to have cancer, this was the one to have.
Obviously, I don’t want any cancer. I don’t want to be treated. I don’t want surgery. I don’t want to have to take medication for the rest of my life. But I also have two little boys to think about, who need their mommy healthy for the next 18 years. So whatever the result is, I will process it, and make a decision. In the mean time I am going to read up on diet, and more natural things I can incorporate into my life- I figure it can’t hurt, and I will be taking a more proactive roll in my health.
Thanks again for all the healing and positive e-mails and comments. I appreciate them so much. As always- I will keep you posted.
**************************UPDATE*******************************
4-13-09
The hospital just called me back, and can fit me in this Wednesday afternoon. I am glad the biopsy will be sooner than later. Now if I can just stay calm between now and then. 🙂