The past two weeks have included many fun activities, but listed among them was my 3 month post-op visits with both my surgeon and my endocrinologist.
First up, I saw my surgeon. Let me just reiterate how much my family and I love my surgeon. The morning of my visit, Caleb was full of questions and curiosity (more than normal) and Piper peed on me (she's potty training and in Pull-ups, but that's another story for another day). My doctor didn't even bat and eye and we were able to carry on a conversation and get a physical exam in during all the chaos.
During my exam, my doctor was checking my incision and also checking for other swollen lymph nodes or lumps. He found none and felt that my prognosis was very, very good.
The next week I visited my endocrinologist and this visit I had the opportunity to see the nurse practitioner, whom I just love. In fact, I have opted to see just her from now on, with the exception of my once yearly visit with the "head" doctor. The last time I saw this NP, I had made an emergency appointment for a racing heart rate and the inability to write or hold a scalpel due to a severe tremor. During that visit, she put me on a beta blocker, a potent heart and blood pressure medication. So, needless to say, this visit was vastly different from the last.
Basically, she went through a long laundry list of symptoms, asking severity and if I was experiencing any of them. Mostly, these symptoms are negative, indicative of disease.
I explained to her that I have felt so terribly bad for so, so long that I wasn't even aware of how bad I was feeling or how sick I was and that now I felt like a totally different, well, whole person. Seriously guys, I haven't felt this well and good since I was probably a young teenager. Anyway, she took a look at all my blood work from August, the day of my whole body scan after my in-patient radiation treatment, during my appointment. Based on that bloodwork, it appears that the cancer is gone. I will have the blood work again in January at approximately 6 months. The only other thing that we had to do was the monitoring of my hormone levels to ensure that I have the correct amount from the synthetic hormone that I will take for the rest of my life. Right now, I am in suppressive mode, meaning that I'm taking a bit more hormone than the average hypothyroid patient. This type of therapy, for at least one year, decreases, dramatically, the ability and chance of any more cancer cells to grown and multiply. From what I gather, after a year on this type of treatment I will be retested, maybe by scan, and my medication will gradually be decreased to normal levels. I just had to up my dosage by a half a pill on Sundays and that's it.
So, that is the long and short of it all. Essentially, I'm well and healthy and waiting for my appointment in January. All in all, I'm super happy and forever thankful that I'm as well as I am!