Jul 26 2007

"Live with it."

Medicine sucks. They can diagnose structural things, and chemical things, but anything functional and they are basically useless. To be fair, scanning organs on a cellular level to tell what's wrong with them is very Star Trek, but one would think they could do something.

I had a CT (structural) following a bunch of blood work (chemical) and an endoscopy (both). The only thing anybody could find wrong with me were some cysts on my kidneys that were so small that ultrasound missed them. One of them had bled a bit, but a urologist assured me that this could not possibly be the source of my pain. The gastroenterologist says he found nothing else on the CT indicating any problem. My general practicioner told me what I basically already knew: medicine can't help me, and I just have to learn to live with it.

A relatively disturbing comment: "I just have to keep you alive until you graduate." said the doctor at the UCR Health Center. I'm guessing it was a joke.

It's not all so bad. My pain is considerably less severe than when this whole thing started, and with a prescription for Donnatol, I am able to manage my pain when it gets bad enough to keep me awake at night. In practice, this has been about 1 night a week. I can eat most of the things I used to, although I'm refraining from pizza and other really bad foods for awhile.

Jul 06 2007

You know what else I think is stupid?

And I don't know why I'm thinking about this right now, but those girls who get tattoos of little wings on their shoulders? I think it looks dumb. Especially when it's very small wings on a very large girl--twee little wings flanking back cleavage are not. good. It's worse even than those asinine NOTW (not of this world--barf) decals people put on their cars.

Jun 26 2007

I want to want you, iPhone

As everyone probably has been unable to avoid knowing, the iPhone launches this Friday. Normally, new Apple releases cause me to sit on my hands to avoid throwing money at Steve Jobs' head, but this one--eh. It's certainly spiffy, in some ways, and the data plan is $10 cheaper than one I pay now for the same service (and $20 less than what Joe Schmo pays), but it lacks key functionality.

Right now I have an iPaq hw6515 that my brother bought for me last Christmas--it's pretty neat, and most importantly, it connects to everything I need it to connect to. Like the iPhone, it has a built-in web browser and email client, but unlike the iPhone, it has the ability for me to install software on it, so it also synchronizes with the Oracle Calendar system implemented at my work. I absolutely cannot do without that--I need my device to remind me to get off my ass and go to my appointments.

Like the iPhone as well, my existing phone/PDA connects to Cingular's reasonably speedy EDGE network... the thing is, Cingular has a faster network, it's available in my area, and the iPhone will not connect to it. Which is Lame-with-a-capital-ell. Why on Earth would I spend $500 for a device that does less and performs about the same as my existing device? Why would anyone (because the iPhone is cooler, I guess)? Besides which, my iPaq is extremely durable. I drop things a lot, the phone not excepted, and the iPaq has been a little trooper about continuing to work after all the abuse I give it. The iPhone, on the other hand, looks like a delicate beast, probably even more so than the Palm Treos that are dropping like flies around me.

I would love to be able to want, and to buy, the iPhone, but that just isn't going to happen. The plan, right now, is to wait for HP to come out with a new 3G iPaq running Windows Mobile 6 (not a smartphone, though), and spend whatever they want to charge me for it, providing it also does all the cool stuff my current iPaq does (bluetooth, built-in GPS, wifi like the next generation of iPaqs after mine has). Isn't it sad, though, that HP of all companies is likely to make a more attractive device, and in many ways already does?

I thought you were cool, Apple.

Jun 20 2007

Diagnostic hell

To begin with: I am not great with needles. I don't get faint, but I am very squeamish. Nurses are fond of telling me that my veins are difficult, but I have, before today, had 2 successful and uneventful IVs inserted.

Today I went in for my CT scan, ordered because the doctor doesn't know what the hell else to do. Last night I had to drink 450 mL of barium sulfate "smoothie", which is way more liquid than is comfortable to drink at one time. The taste starts out pleasant enough, but by the end is associated with a queasy, stuffed feeling. After that, no food or water.

8:15 am, show up (on time) for my CT. They give me another 450mL bottle of barium sulfate to drink. Shit. Over the next 2 hours, as I wait, I choke down the milky liquid, its "berry" taste now imprinted as something grotesque. And I pee a lot, because I'm downing another half liter of liquid.

Finally, I'm called and led into a small waiting room, after changing into a gown. The nurse is going to start my IV. No problem, think I, since the last couple times went without a hitch. After all, this person does this procedure all day, every working day.

Start with my right hand. Tie it off, hit the fuck out of it. There's the vein. Giant needle, *sting* (normal), pain (huh...that didn't happen before), FUCK, PAIN!

Me: "Ouch! Christ!"
Nurse: "oops, it blew out the other side."

For her second attempt, while my right hand is still stinging like fuck, she warms my left hand. More tying, more hitting.

Me: "Ow, ow ow OW OW OUCH SHIT!"
Nurse: "oh, oh no it did it again." (notice "it". Not "I")
Me: *stares at her with palpable hate*
Nurse: "I'll just go get Lupe"

Now both of my hands are bandaged and quite painful. In what happens next, let me know if I'm out of line here, readers.

Lupe: "ok, we're going to try in another place. Oh, he looks like he's going to faint."
Me: (yelling) "I'm not faint! I'm in pain!"
Doctor: *peeks his head in. Makes a quick retreat.*

The new lady, Lupe, then proceeds to warm, tie, clean, and properly insert the IV the first time. The other nurse will avoid talking to me the rest of my time there.

I was then led into the CT room, where I was given ANOTHER GLASSFUL OF BARIUM. This one is "banana", and even worse than the previous one. Thankfully I think I was only given about 150mL of it. I then lay down on the table, my arms held over my head. The table moves up and then through a ring with a rotating x-ray machine. The disembodied voice says "take a deep breath and hold it" in a peculiar tone, almost as if the words themselves have no meaning. The table scans slowly through, and I got "and you can breathe" in an equally unconvincing tone. He says it like "and you can breathe! Which makes you superior to fish!"

They then pushed the contrast (iodine) into my IV. Lupe warned me: "they keep it hot, so you're going to feel really warm". Shit, she wasn't kidding. Instantly I felt like I'd been running. I was hot as hell and my heartrate climbed rapidly. They ran me once through the machine again, and I was done. The actual procedure lasted 5 minutes. The mental trauma will last a lifetime.

Jun 10 2007

I really wish I knew what was wrong with me

For 7 weeks now, I've had some kind of weird ... condition. Severe abdominal pain woke me that night at about 3am. I thought I must have food poisoning, got up, threw up. In retrospect, what I was feeling was not nausea, but it's hard to tell sometimes with such pain, and I thought it was a sensible course of action.

The next morning I felt mostly ok. I could eat. I had no symptoms of food poisoning. That night, pain set in an hour after dinner. The same pain: in the upper abdomen, sometimes a feeling of tightness on the right side, sometimes with a pulsing of the abdomen, accompanied by chills from time to time. Then the next day. Then the next.

That weekend I got to the point where I thought I should go to Urgent Care. I was up all night with severe pain. They x-rayed me, gave me an antacid cocktail, and sent me on my way. Never mind that the cocktail didn't stop my pain.

I survived the weekend until my appointment with my usual doctor at the campus clinic. He stated that I probably had gastritis or a peptic ulcer, and gave me prilosec and pepcid. He screened for H pylori, which was negative. I started the medication, to little avail. Even on a rather limited diet (think chicken, bread, veggies, and water), I was still having pain every night. Even after doubling both dosages, my pain was roughly the same.

When, a week into treatment, it was clear that I wasn't getting better, the doctor referred me to a gastroenterologist. The insurance company gave me a short list of local GI specialists, all of whom were booked for months except one. Thus, he became my doctor. While waiting for the appointment, I had my regular doctor screen for pancreatitis with a blood test, which was negative.

A few days later, I was sitting on a bed in the gastroenterologist's exam room. He entered the room, and indicated that I should walk across the room and sit in a chair that was there, so that he could sit in a chair near the door. He wanted me to be as far from him as possible, evidently. What followed was not really an exam, but a short question and answer session. He glanced at my chart, test results, and ordered an endoscopy and ultrasound.

The endoscopy went fairly smoothly. It was scheduled for the following morning, so no long waits. I went in, they inserted an IV, pushed a general anaesthetic, shoved cameras and tools down my throat. I woke up with a sore throat and a hiccup that would last several hours, but all-in-all it wasn't a bad experience. The nurse told me (I did not see the doctor after the procedure) that they saw no cancer and no ulcer. They did a biopsy for H pylori, in case the blood test had just failed due to a lack of antibodies in my blood. I found out a week later that that biopsy was negative.

At each stage, of course, I hoped that they would find something. It seems odd to be praying that you have an ulcer, a bacterial infection, or even pancreatitis, but actually anything treatable is better than a mystery. If it's a mystery all they say is "go home and tough it out." The ultrasound came and went, almost 2 weeks ago. I get the results on Tuesday. I thought of urinary tract infection, and visited my doctor who did a urine test, but of course it was negative.

Then something really shitty happened. I started to feel kind of better. I could eat sugary stuff. I had a hamburger, and some french fries, with little to no pain. I went almost a week with no problems. Until tonight. Ice cream, which had never caused a problem before, and here I am up at 4 am writing this blog post in pain instead of sleeping.

Did ice cream cause it? Is food involved? Neither antacids nor tylenol seem to help 100% of the time. One or the other seem to help, but it's difficult to say. Then one starts to get ideas. Maybe it's an aortic aneurism! I feel a pulsing! But it's improbable, and likely the internet is just scaring me. Looking up one's ailments seems like a comfort until you hit the search button on google. Then you just start being terrified at all the ways you might be dying. You think, "well, yes these ailments are rare for someone my age, but so is chronic abdominal pain." Suddenly, in light of your obvious pain, unlikely conditions seem entirely plausible.

I fear that when I finally see the gastroenterologist again, in 3 days, 4 weeks after my first visit, that he's just going to say that it's a mystery. By then they will have probably ruled out gallstones and aortic aneurism with ultrasound. In that case, I will have to content myself with my present condition of only 1-2 bad days every week, and hopefully I can keep my weight steady at 137, down 10 lbs from where I started but 5 pounds heavier than my lowest during this ordeal.

Yeah. I don't have any cute or clever way to finish this. I hurt and I'm scared. Just thought some people might want to know.

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