Archive for July, 2013

BMWotD — e36 Compact with M50 Six

Friday, July 26th, 2013

It’s been a while since I last posted a BMWotD, and I’ve got a few of them stashed away on my local drive, so time to play some catch-up.

This one was listed for sale on the Minneapolis CraigsList earlier this month, and had (un)fortunately sold before I saw mention of it on the 318ti.org forum recently. Looks to be a nicely executed swap on a very clean car. Loving the interior on this car too. The asking price may have been a little on the high side, but the fun factor combined with the clean factor plus my favorite color would’ve made it hard to pass up. Good thing I didn’t have the chance to deliberate whether to take a shot at it.

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Some Serious Progress

Wednesday, July 24th, 2013

Another very tardy update; the last few weeks have been, um… eventful.

Four weeks ago I had my first sit-down with Dr. McGraw, the radiation oncologist. There was a bit of a snafu in the scheduling, as he would’ve preferred to have seen me after my PET scan (which was done the following Thursday morning; more on that later) so he didn’t have a full game plan for treatment. He also said that he would be passing my case over to one of his partners because he was being deployed with the Air Guard and would be gone for the next three months. He did however take the time to explain things pretty well, so Yvonne & I were thankful for that. Knowing what he did of my case (two things you don’t want to hear from a doc; “I’ve been reading up on your case; it’s very interesting.” and “Wow, I’ve never seen [i]that[/i] before!”) he thought that a course of 18 daily radiation treatments over a span of three weeks ought to do the trick to completely eradicate the cancer from my jaw.

The treatments would be aimed at my jaw, and should only affect that immediate area; the side effects didn’t sound like much fun (and haven’t been) but he didn’t think it would interfere much with life & work (they haven’t, much) and should be effective. The daily thing was kind of a surprise, but he explained that doing smaller doses daily is far easier on the body than larger doses spaced further apart. I think I can accept that; I won’t enjoy it, but that pretty much goes without saying.

Following the appointment that morning I was also fitted with my Hannibal mask. They don’t call it that, but I will because that’s the first thing that came to mind when I saw it; it’s a form-fitted mask that helps to keep my head stationary during the radiation treatments, and also allows the techs to mark it up with reference points so they can be more consistent from one treatment to the next (which is better than marking me!) It’s made of a plastic mesh that starts out flat and becomes pliable when warmed up. The techs draped the warmed mesh over my face, then fitted it to a u-shaped plate that clamps to a hard plastic headrest. This isn’t mine, but looks an awful lot like it:

Since the tumor is on my lower jaw, they also want to keep my mouth from moving, so I was fitted with a mouthpiece, which is similar to a football bite-guard except it has a flat plastic piece in place of the part that would normally form fit around the lower teeth. After the initial fitting, the bite-guard was attached to the mask; the two combined, with the mask clamped onto the headrest, with me in a supine position on the table made for an extremely unpleasant confined feeling.

They did a quick CT scan of my head that first Tuesday, and in the few minutes that it took I nearly gagged on the stupid mouth guard. The bite guard obstructs my tongue’s movement, and that combined with the way the mask fits around the bottom of my chin made swallowing really difficult. And that combined with laying flat on my back on the table made for a few moments of near panic. I made it through the CT scan, and was so glad to finally be released from the thing I failed to say anything about that. Later I assumed that at some point we would take some time to get the mask & bite guard to fit better… Wrong assumption.

During our visit Dr. McGraw mentioned that he wanted to use that mask for my second PET scan in order to get more accurate results; I was still hoping that there might be some adjusting we could do with it, but when the nurse trotted that thing out on Thursday morning it was pretty clear that wasn’t happening. They got me ready and slapped that puppy over my face & told me to relax, the test would take 20 to 25 minutes. That’s when I nearly lost it.

I was to have nothing but water for six hours before the PET scan, and part of the prep involves drinking a thick sugary goop. That made for a bit of sticky gunk in the back of my throat that was hard to swallow. Add to that the bite guard in my mouth and the part of the mask wrapping under my chin and it was extremely hard to swallow. I’ve never considered myself to be claustrophobic, but I’d never been this restricted before (having my arms strapped to my sides didn’t help that either.) I knew I wouldn’t be able to make it five minutes, much less twenty-five minutes, so I grunted and kicked and did whatever I could to communicate to the nurse that it wasn’t gonna fly… She pulled the mask off and I nearly hyperventilated, so happy to be able to breathe again!

I explained the difficulty I was having, so she went to ask about adjusting the thing; she came back saying the word was ‘no’ on adjusting, but the doc relented on the mouth guard, and she pulled it off of the mask. The mask was still somewhat restrictive, what with the part that wrapped under the chin, but I somehow made it through the procedure by praying, reciting what I could of the 23rd Psalm (sure felt like the valley of the shadow of death!) and counting. The PET scan operates by making scans of small sections of the body, as if it’s a great big meat slicer (that thankfully doesn’t actually cut anything.) From the counting I determined that it took around three minutes for it to scan a section of my body; then the table I was on would move forward six inches or so, then it would scan the next section of my body. I lost track of how many times it moved, but if my one-second counts were accurate, it was about three minutes between each move.

Even with the counting and praying, there were still a few moments where I was this close to bailing out; swallowing was difficult, breathing was difficult, I was getting a kink in my neck from the plastic headrest, and having my arms & legs strapped down was just a bit too much. But I did make it through. Later on I realized another factor that made the earlier PET scan so much easier; Dr. Bleeker prescribed a sedative for me to take in preparation for the test. I think the mask would still have been a problem if I’d had the sedative on board, but I have no doubt that would’ve helped.

Later that same afternoon we met with Dr. Bleeker to go over the results… The PET scan basically measures the glucose uptake of cells in your body. To do that, a radiotracer is injected into the bloodstream; for cancer detection, the radiotracer used is FDG (fluorodeoxyglucose) tagged to glucose. Cancers absorb glucose differently from normal tissue, and the PET scan is able to detect those differences; in reading the PET scan, a radiologist reads the scan results and grades the “glow” of an area in SUV (Standardized Uptake Values). When I had my first PET scan back in April, the glow in my jaw was a 10; following chemotherapy it was 3. Considering the fact that normal or benign tissue has an SUV of 2.3, I’d say we’re heading in the right direction.


I started writing this post about three weeks ago, and am just now finishing it up. I could go on, and tell more about the radiation therapy, but I think I’ll just post this and start a fresh post on that topic. Pretty sure I can finish it in less than three weeks. 😉

Godspeed, Ken

Friday, July 12th, 2013

A good friend — Ken — found an end to his earthly suffering today, losing his battle with mesothelioma.

I’ve known members of Ken’s family much longer than I’ve known him, so it feels like I’ve known him forever. In reality though it’s only been about 15 years or so. Ken is a few years my senior, and has been retired longer than we’ve been acquainted. He’s not exactly an official mentor, but he has mentored me on many levels, usually unintentionally. Such a great guy; quiet, humble, honest… Seems like they don’t make men like anymore, or at least not as often.

Ken’s mesothelioma diagnosis came long before I was diagnosed with DLBCL, but we somehow ended up on the same rotation for chemotherapy; I counted him as my chemo-buddy. Mesothelioma is a much different and more aggressive cancer than DLBCL, and his fight was simply for a little more time; there is no cure, and the chemo only slowed its advance until it outsmarted the drugs. He had explored lots of treatment options in the last few months at Sanford Cancer Center and at Mayo Clinic, but the doctors said there was little more they could do for him and he wouldn’t likely see Christmas. I really hate it when they are that right.

The last time I saw Ken was two weeks ago this Sunday; Ken was admitted to the hospital a week earlier, and Yvonne and I stopped to visit, staying much longer than we had intended. I’m glad we had that time with him. Ken looked good that day, alert but a bit sleepy from the drugs helping to control his pain. The cancer had spread to his abdomen and had formed several tumors which were collecting fluid and causing a lot of pain. He and Harriet were so grateful for and hospitable to every visitor; the embodiment of graciousness. The strange thing was that only three weeks earlier at our last chemo session he looked great and was in no pain at all. That was five weeks ago, and today he’s gone. I just can’t wrap my head around that.

But Ken was well grounded in his faith in Jesus Christ, and there’s no doubt he’s in a better place now, free of pain and worshiping at the Throne. It’s hard though, knowing I won’t see him again, and knowing how difficult this will be for his family. Still, I envy him just a little… But I know it’s not my turn yet; God still has a job for me here, so I wait patiently for him to call me home, and try to become what he wants me to be.