My bloodwork from Monday’s oncology visit indicated elevated sodium and depressed magnesium. We’re not clear on why I would show elevated sodium, except as possibly an accident of diet over the preceding weekend. The magnesium depletion is a known side effect of Vectibix. Though I’m already taking a magnesium supplement, I now have to double that up. Since magnesium, like calcium, is contraindicated with my Doxycycline, I have upgraded to a four-times-per-day pill routine. Oi.
The bloodwork also showed my liver functions as continuing within normal ranges. This means whatever’s going on with the elevated CEA levels hasn’t yet grown large (or fast) enough to impair my liver. That’s relatively good news, as the swiftness of the recent spike in CEA levels, combined with my recent metastatic history, had led me to fear a wildfire metastasis moving very quickly through my body.
As of Monday, CEAs were at 6.6, up slightly from 6.4 two weeks ago. That amount of variation is within the margin of error of the testing process. Since one of my fears was a sharply uptrending CEA, in a weird way, this is good news. It’s also bad news as it confirms the overall uptick from March’s 2.9, which implies with near-certainty new metastatic tumor activity, probably in my liver. I will know more on 5/8, after my 5/7 CT scan. I have also queried my oncologist about the value of getting bloodwork done on 5/7 (ahead of my usual schedule) in order to have the most current information when we meet.
After a conversation with the American Cancer Society reps in the infusion center Monday, I am pursuing an appointment with the oncology social worker to discuss support resources in the somewhat likely event I receive a difficult diagnosis on 5/8. We’ve been playing phone tag thus far. I’ve made it the past five years without feeling the need to seek a support group, but when I go terminal, I suspect I will benefit from something like that, as I’ll be further outstripping the resources of my circle of friends, family and loved ones. Likewise, looking to such support for
Planning Ahead for Liver Failure
I am also pursuing an appointment with the oncology nutritionist to talk about how to eat in the context of progressive liver failure, as seems to be a likely future course. Even if this round turns out to be something other than liver metastases, liver mets are my most probable fate. As mentioned before, I am also meeting with my primary care physician on 5/10 to talk about the course of liver failure and what kinds of advance planning we may want to do with regard to treatment decisions, cognitive issues and so forth.
Dealing With Photosensitivity
A while back, Team E— turned me on to a line of clothing from Loki. They’re climbing wear, but they turn out to work really well for people with extreme photosensitivity. (i.e., me.) Basically, Loki makes jackets and hoodies at various weights which include hoods much deeper than normal, face masks and optional mittens built into the sleeves. It’s some pretty clever stuff.
The problem is that the first hoodie I bought was in black, and when I have it on in full sun aversion mode, I look like I’m about to rob a convenience store. So we got one in green. Which mostly makes me look silly. Which fine, because silly is less scary to other people.
At any rate, Loki gear is highly recommended if you or someone you know is dealing with chemo-induced photosensitivity. (Or photosensitivity for any other reason, I suppose.)
Skin Conditions and The Itch
Another piece of advice on living with cancer that turns out to need a signal boost cropped up during last week’s Reddit Fantasy AMA chat, of all places. That has to do with dealing with skin conditions and the damned itching from (in my case) Vectibix. There are certainly other drugs which create this problem as well. Almost every night, I take a baking soda bath. Like you might do for poison ivy. I use the equivalent of a box of baking soda, though we buy it in large bags from Costco, poured into water as hot as I can stand to be in. I then soak myself in various positions to get as much coverage as possible. This also tends to make me very sleepy, which combined with the reduced itching, leads to a much better night’s rest. My skin winds up feeling a bit slippery from the baking soda, which takes a bit of getting used to, but I also take a shower every morning. So, as with the Loki gear, if you or someone you know is dealing with chronic skin conditions or itching, this is highly recommended.
Photo © 2013, Lisa Costello.
This work by Lisa Costello is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 United States License.