Aaaaaaugh.
Just so I can keep track of this - feel free to scroll if health stuff bores you. I'm feeling SarahK when she complains that she knows more about her celiac disease than her doctors do. As y'all know, I have chronic pancreatitis (the hereditary kind, not the alcoholic kind - the only drink I've ever had is one drink of champagne at my cousin's wedding. Yes, I am Sandy from Grease, without the leather pants.)
I was part of a genetic study in the 90s that mapped the gene to chromosome 7. The molecule that keeps trypsin inactive until it leaves the pancreas (the molecule is called PTI, if I recall correctly) is messed up, so trypsin gets activated in the pancreatic duct and chews up the pancreas. Not fun. And I'm convinced that mine is exacerbated by stress, because I've been in constant pain since I started medical school, the most stressful time of my life.
For some reason, for the past couple of days, my pain isn't even controlled with my Vicodin HP (hydrocodone/APAP 10/660). As an aside, my GI doctor sent me to a pain clinic, and I went with a current dosage of the 10/660 as 1 tablet q6 prn. (One every six hours, or 4 per day, as needed.) The pain clinic (at which I saw a physician's assistant, not a doctor) gave me a lecture on taking pain medications (I think that in order to work in a pain clinic, you should have had chronic pain yourself. You know? I don't WANT to be on pain medication, and I usually hate when people pull "rights" out of nowhere, but I believe that people have the right to be comfortable and functional if possible. I think it's part of the "pursuit of happiness" thing.) So after the lecture, at which point I felt like crapola, the PA gave me a prescription for a 25mcg/hr fentanyl (duragesic) patch. This is what my GI doctor and I thought might be a good option for me, along with something short-acting for breakthrough pain, because it would work well when I was at the hospital working for hours and hours without time to eat, drink, or pee - and it also provides a constant, steady medication level - no more peaks and painful troughs, and no more chronic ingestion of liver-munching acetaminophen. Everybody wins.
So the first day that I wore the patch was painful, because they didn't give me anything for breakthrough pain and the patch takes about 12 hours to get into systemic circulation. But once it was in - MY PAIN WAS GONE. I woke up the next morning with no pain, no grogginess - it was so great that I thought I was dead and in heaven. And then I saw that I was still fat - no glorified body. But anyway, later that day, I started feeling weak, dizzy and lightheaded. The next morning was even worse. I couldn't get through to a human on the pain clinic's line, so I just went there (and got scolded because they usually ignore walk-ins.) LUCKY FOR ME, they said, they weren't busy. So they removed the patch, told me to bring the rest of the patches back, and gave me a prescription for the 10/660, 3 per day. The pain clinic gives me less pain control than my GI doctor. Great.
Like I said before I got on the pain clinic tangent, for the past couple of days, I've just been in horrible, intractable pain. I didn't know what to do besides go to the ER, so to the ER I went. (And I'm not a revolving door patient - I haven't been to the ER for at least 6 years.) The first ER visit, on Wednesday afternoon, didn't work out because there were approximately three million people waiting, and I didn't want to wait there for the rest of my life. They told me that it clears out in the wee hours of the morning, so at the wee hour of 3AM, I went back. This time I saw a doctor, but it went horribly - the doctor was an evil man who missed the day that they taught empathy and compassion in medical school. He also wouldn't listen to me when, after he told me that my amylase and lipase weren't elevated (translation - "You're a lying, thuggish drug-seeker"), I told him that when pancreatitis is chronic, the cells are so damaged that the enzymes don't usually go up anymore*. They did give me a shot of Dilaudid and Zofran which was heavenly considering I've been in miserable with no relief for 2 days. I thought they'd admit me to let me be NPO and let the evil pancreas rest for a day or two to possibly break the pain cycle, but since the doctor could tell that there's obviously nothing wrong with me because the magic enzymes didn't say so, they didn't. I left there crying because they made me feel like a liar and I knew I'd be hurting again in several hours. And I'm beyond worried about missing clerkship days. I hope I don't get kicked out of medical school, and I hope I don't end up with a different class (no offense to the c/o 2010, but my class is just so awesome and I ::heart:: them. Except one. He knows who he is.)
I called my GI doctor when I woke up from the lovely Dilaudid fog, and told them that the experience had been horrible. They told me that I should call my primary care doctor, who I should have given the ER as my doctor (what do I know? I was there for a GI problem, so I gave them the GI doctor's name. Oh well.) Problem is, my primary care doctor is not in the office today, and the doctors on call for him are all, "Her enzymes must be elevated or she's a malingerer. A MALINGERER!" I'm likely to leave with a diagnosis of Munchausen's Syndrome, but I'm headed back to the ER. I want a couple of days to be NPO, with an IV so I don't get dehydrated, and pain control until this thing breaks. I've got things to do, y'all. I have the weekend to get better, and I hope I'm still a medical student on Monday.
Labels: DoctorsWhoAreIgnorant, MedicalScruel, MyEeeeeevilPancreas, OtherBlogs, PainClinic











