Reader(s):
Well, thanks to the doctor/detectives at the Mayo Clinic, we have now solved the mystery of the High-TG levels.
Before I reveal the culprit, I would like to describe my Mayo experience from the beginning. Also, like any good mystery writer, I just want to build up some suspense.
First of all, this place is freakin' ginormous. And swanky. Mayo Clinic pretty much takes up all of downtown Rochester, and its various buildings are all connected to each other and to nearby buildings and hotels via an extremely impressive network of underground tunnels (although it's all foot traffic they call it the subway) and above-ground skyways. There are all kinds of cool things interspersed around the first floor and the subway such as a Mayo history display, tons of artwork, a Cancer Education Center that has Yoga and Tai-Chi classes almost every day, and lots of various shops and food stores.
The main building is nineteen stories high. The endocrinology department, where I spent most of my time, is on the eighteenth floor. Despite the huge number of doctors and patients and facilities, everything at Mayo is super-efficient. Yesterday I had one of the fastest blood tests of my life, despite the fact that there were at least 20-30 people in the waiting room with me. My procedures today were very efficient also. Overall my mom and I were extremely impressed about how well everything was done. It's pretty clear why this place has such a great reputation.
So now that we have the setting down, I'll explain what actually happened.
When I first met with the doctor yesterday morning, he basically told me that he didn't think having an RAI treatment at this stage is a good idea. Since we would be essentially just treating a number (my TG level) without any other evidence of cancer, and since I'm young and my type of cancer is very slow-growing, he told us that he would prefer to wait and see what develops rather than give me a high dose of RAI without knowing if it would even be effective, especially since high RAI doses can have negative side effects in the long term.
He ordered a blood test and an ultrasound, and told us that their radiology department often finds things when previous scans haven't. So I had a blood test yesterday and an ultrasound this morning. The ultrasound did show two suspicious lymph nodes, and I had one of them biopsied right away. When I met with the doctor again this afternoon he told us that the biopsy was positive. Which means we have now found our culprit. It's a sneaky little node on the left side of my neck near my collarbone, right near my scar. Tricky little bastard.
One of the things the doctor explained was that because papillary thyroid cancer is so slow-growing, cancerous lymph nodes can take a long time to develop to a size that can be seen and/or treated. Yesterday he told us we should start thinking of my cancer as a chronic disease, rather than something that needs to be gotten rid of urgently like other cancers. I still don't know how I feel about the idea of having to go through this again and again for the rest of my life. I suppose it's better than having a bad long-term prognosis, but it also means I have to keep waiting around and that's pretty much my least favorite thing ever. Patience has never been a virtue that I have possessed.
Nevertheless, we have decided to wait for another few months or so before we take care of the aforementioned lymph node. Normally I would have it removed surgically, but since I just had surgery in April the doctor said he would prefer to wait at least a year before having another one. And I'm certainly not thrilled about going under the knife again so soon.
Also, Mayo has recently pioneered a procedure called alcohol ablation that they've been using to get rid of metastatic thyroid cancer lymph nodes in the neck. From what I understand, it involves using alcohol to blow up the cancerous lymph nodes rather than removing them surgically. Mayo is one of the only places in the country that does this procedure, and the doctor said he would talk to the radiology department about whether this is a possibility for me. If so, I'll probably come back to Mayo within the next six months or so and have that done.
No matter what, I probably won't have RAI again. At least not for a long time. The doctor said that lymph nodes usually don't respond well to radioactive iodine, and since mine didn't show up on the RAI scan last month it doesn't seem likely that they would be affected by an RAI treatment anyway. I'm pretty happy that I don't have to go through it again. All my other doctors have talked about how it's a magic bullet and it's super effective for thyroid cancer and blah blah blah, but I kind of think it sucks. At least when I'm going through it. So good riddance, RAI, LID, and all you other stupid un-fun acronyms.
Unfortunately that does mean I won't be radioactive again for some time. I might have to change my pen name. Any ideas? Thyroid Diva, maybe? Papillary Princess? Given that I've now had three biopsies in the past year I've been considering calling myself the Biopsy Queen. But maybe that one's not so good.
For now, I'm going to go back to my life, but I'll probably be back here in Rochester soon. And I will try to keep updating about cancer-related issues when they arise and/or whenever I actually have time to sit at my computer and write things.
Homeward Bound,
RG
Documenting my life of cancer treatment: from crappy diet to total banishment from human society and everything in between.
Showing posts with label biopsy. Show all posts
Showing posts with label biopsy. Show all posts
9/24/2010
8/12/2010
Cancer Limbo
Dear reader(s):
Well, I promised you updates, so here goes:
Biopsy was today. It went fine. This was my third so I'm pretty much used to them at this point. I was, in fact, filling out paperwork beforehand and had some trouble fitting in my answer to the question "List any other biopsies/surgeries in the affected area along with dates and hospital names". If I were Jeff Foxworthy the joke here would be, "You know you're a cancer patient when...your list of past procedures looks more like a novel than a list".
Or perhaps more cleverly worded than that. But you get the idea.
Anyway, the whole thing was pretty routine. They found the lymph node they were looking for (sort of behind my right lower jaw area), stuck me nine times with a needle, sent me home. The radiologist told me before she left that she'd gotten a quick look at about half of the samples and hadn't seen anything yet that looked cancerous. So...so far so good I guess. Official results probably won't be in until tomorrow afternoon, but we explained my situation and the doctor said she'd try to get them done as soon as possible.
Until then, we remain in Cancer Limbo. My absolute favorite place to be, where birds sing and flowers blossom, and candy gumdrops rain from the sky. Ah, Cancer Limbo. Just one of the many scenic Sick World destinations for you to choose from. Or, actually, not choose, because you're stuck in Sick World whether you like it or not. It's like the Hotel California, but less fun and without an awesome song.
So, dear reader(s), that is all I have to tell you until tomorrow. I would send you a "Wish You Were Here" postcard, but that would be cruel.
Love,
RG.
Well, I promised you updates, so here goes:
Biopsy was today. It went fine. This was my third so I'm pretty much used to them at this point. I was, in fact, filling out paperwork beforehand and had some trouble fitting in my answer to the question "List any other biopsies/surgeries in the affected area along with dates and hospital names". If I were Jeff Foxworthy the joke here would be, "You know you're a cancer patient when...your list of past procedures looks more like a novel than a list".
Or perhaps more cleverly worded than that. But you get the idea.
Anyway, the whole thing was pretty routine. They found the lymph node they were looking for (sort of behind my right lower jaw area), stuck me nine times with a needle, sent me home. The radiologist told me before she left that she'd gotten a quick look at about half of the samples and hadn't seen anything yet that looked cancerous. So...so far so good I guess. Official results probably won't be in until tomorrow afternoon, but we explained my situation and the doctor said she'd try to get them done as soon as possible.
Until then, we remain in Cancer Limbo. My absolute favorite place to be, where birds sing and flowers blossom, and candy gumdrops rain from the sky. Ah, Cancer Limbo. Just one of the many scenic Sick World destinations for you to choose from. Or, actually, not choose, because you're stuck in Sick World whether you like it or not. It's like the Hotel California, but less fun and without an awesome song.
So, dear reader(s), that is all I have to tell you until tomorrow. I would send you a "Wish You Were Here" postcard, but that would be cruel.
Love,
RG.
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