Wednesday, September 7, 2011

Digestive System Fail

This is one of those [more than sufficiently long] ramblings that is more for my memory's sake than anything else. But for those curious and non-squeamish types, feel free to read on.

I can't pinpoint a date when I started having pain in my stomach, so sometime in the last four years I began having mild to major pain in the upper center part of my tummy. Usually it just annoyed me, but every now and then I would feel so sick that I could hardly get out of bed. I'd feel nauseated and get weak and lightheaded and sweaty. I couldn't seem to find a remedy, either. Of course, I'm not much of a seeker of medical attention, so I waited until my annual physical last fall to ask my doctor what might be wrong with me. He ordered an ultrasound to look at things and sent me on my way. The ultrasound revealed that -voila!- everything was normal.

Talking to the doctor again, he suggested I get a HIDA scan done. I scheduled it, but after consulting with my health insurance people and finding out how much those fandangled tests cost, I decided to
forgo. No stomachache deserves that much attention and financial gratification was my opinion, especially at the end of the year when we hadn't paid hardly a cent toward our deductible. So I persevered.

The new year brought what seemed to be a worsening of my symptoms, so I revisited the idea of further testing. Then when we had some changes to our health insurance which would raise our deductible considerably, we decided it would be best to go for it before the changes became effective. My doctor worked his magic to rush the orders before the deadline, which was about 2 weeks away.

The HIDA scan came next. The procedure for this test consisted of getting an IV through which some radioactive dye was sent that lit up the gallbladder while I lay under a big x-ray machine for a couple of hours. This was about as bad as it sounds. The IV and dye didn't bother me [although I'm not generally a big fan of sending radioactive products coursing through my body], but lying still on a hard, narrow table for that long about did me in. I brought along my current book club read
[which I think was The Brother's Karamozov -- oi! I needed something much more diverting], but holding my arms above my head and avoiding all the contraptions was not so fun. After the gallbladder was sufficiently visible the technician added some hormone to the IV that made the gallbladder contract so they could view if it was properly dispensing it's juice. Upon observation, the conclusion came back... Normal!

Next came the CT scan.
Of all the procedures, this was my least favorite. It was quick, which I appreciated, but whatever junk they stuck in my veins I felt certain was going to kill me. The technician warned me I'd experience some sensations such as feeling very warm and like I was going to wet my pants. Nice, huh? So they started the IV and told me to follow the instructions the machine would issue. "Breathe in ... Hold your breath ... Breathe out." It started out all right, but as the contrast spread through my body, I got horribly hot. I began feeling a little bit panicky. I have no idea what a heart attack feels like, but that's what I imagined as my whole center heated up and felt compressed. And I truly thought I would wet my pants. So weird, and utterly unpleasant. Fortunately, it was over in a timely manner and my pants stayed dry. I left the hospital and decided to run a few errands before heading home.

Here's where the fun began. I arrived home to a very disturbed husband. I think his first sentence to me was, "I'm getting you a cell phone!" [Yep, I'm one of the 13 people in the US who does not yet have a cell
phone.] Apparently, immediately after I left the hospital, the radiologist called to say that I needed to either go to the emergency room or to my OB/GYN right away. The scan showed that my IUD had ruptured the wall of my uterus and needed to be removed promptly. Jeremy took the liberty of scheduling an appointment with my doctor, so we went to investigate the matter. Now it turns out I had just been to see the midwife at this same office to determine the cause of some other pain I'd been having. She had ordered an ultrasound which showed some ovarian cysts. Nothing too worrisome. So the doctor took another look at the ultrasound and declared the IUD to be in exactly the right place. He called the radiologist, who stuck to his determination that there was a serious problem. My doctor seemed unconvinced, since I didn't have signs of infection, but he also couldn't argue with what the radiologist said he saw. So he removed the IUD prepared to send me into surgery if it was indeed ruptured through the uterus. But, as seems to be a theme here, everything appeared normal. He sent me home with some antibiotics, just in case, but still sure that everything was just fine.

Test #4: Endoscopy. Actually, it had a much longer and more impressive sounding name, but I'd have to go find the paperwork to write it all down. For this one I would be sedated and the surgeon would stick a camera down my throat to take a look at my insides. I was a little nervous about being knocked out. But it ended up being the best part. I remember them hooking me up to the IV. They put something in my mouth so I couldn't bite down. It also made it so I couldn't talk. My arm started to hurt where the IV was placed, so I thought I would take the thing out of my mouth and ask if that was normal, but I
couldn't do it and then I was asleep. When I woke up I was so disappointed. I'd been having the best, most restful nap ever. I wanted so badly to stay put. The surgeon came in and showed me some pictures of my small intestines and began explaining that the little teensy lesions I saw were either caused from celiac disease or from ibuprofen use. Of course, my brain was a little foggy still and I couldn't get over the fact that I had pictures of my gut. Cool! He ordered a blood test and said they'd taken a biopsy to rule out celiac disease. Jeremy walked me to the lab for the blood test, and then we left to go curtain shopping. The doctors had instructed me not to make any major decisions for 24 hours after the sedation, but I'm happy to say I still like the drapery I picked out in my altered state.

I spent an anxious few days thinking of all the things I would miss if the celiac diagnosis was confirmed. And, naturally, I ate as many of them as I could. I thank my lucky stars that the tests came back normal. Which meant
I was having a disastrous reaction to ibuprofen. I've steered clear since then and am pleased to report I have mostly felt much better. I still get minor stomachaches from time to time. But I haven't had any severe problems for a few months. Still, I think the best part of the whole thing was getting a picture of my tummy from the inside. It's so fascinating. If this sort of thing bothers you, you can't say I didn't warn you. Look away!

Saturday, August 27, 2011

More Morganisms

Morgan sure makes me laugh. Here are a couple of her most recent funnies:

I walked into her room to find her dresser draw emptied onto the floor.

"What happened here?" I asked.

"I didn't do it!" she retorted. "Daddy did it."

"Oh, yeah?"

"Yeah! He was sleepwalking."

Where did that even come from?!?

Then today, I was getting her out of the bath. She hollered and cried in protest.

"But then I can't swim!"

I didn't think that should constitute the end of the world, but apparently it did because then she explained, "I'm a mermaid. I have fins. I can't walk because I trip on them."

Oh, Miss Morgan the Mermaid! You certainly color my world!

Wednesday, August 3, 2011

Goals Met & Made

Goal met: Today I ran 3 miles for the first time. This might not seem like a big deal to some, but for me [total non-runner], I was feeling pretty swell.

Goal made: Someday I will take a vacation after which I will feel better than I felt before I left. Not sure when or how this will come to pass, but it must. MUST!

Sunday, July 24, 2011

Milestones

Party time at our house! Morgan turned 4. We had a fun family celebration, followed by a "Pinkalicious" friend party. She asked for a princess cake, so I had my first foray into the Barbie-doll-cake-in-a-bowl tradition and experienced varying degrees of success. The party was received enthusiastically. When I went shopping for all the pink accoutrements, it looked like a Pepto bottle exploded on the checkout counter. I made pink tutus for all the girls; we decorated pink wands and ate pink cupcakes; the girls got their fingernails painted - pink, of course; we had a pink Jello jiggler race and made pink bead necklaces. Good times all around. I felt like it was a hit when one of the girls told her mom, "This was the best day of my whole life!"

I achieved a goal of mine recently. It only took four years. I finished
writing the story of Morgan's first month of life. It really shouldn't have taken so long, but I started and stopped many times. It was a hard story for me to visit. I wanted to record it all, but the memories were emotionally intense. Much of the experience has become a blur, and I hope I captured the most important details. In particular, it was a spiritually defining time, and those are the things I feel are the most important to remember.

I won't recap the whole story here. Many of the details are too personal and near to my heart. [Not only that, but I filled about 10 pages. Nobody wants to read all that.] But for anyone who doesn't know the basic story, Morgan was born with a malrotation of her small intestines. She was admitted to the hospital at 10 days old, spent a week with doctors trying to fix her in all the wrong ways, then had surgery at 17 days old which put her on the road to healing and health. So many worse things could have happened, and I count my blessings that the end result was positive.

Four years later, I still look at Morgan’s scar almost every day. It doesn’t look so big and ugly now. A little part of me hurts when I see it. But mostly my heart soars. I like to kiss the three little white scars from the picc line on her arm. They’ll always be there, especially noticeable in the summer when she gets a tan. They remind me of the life I could have lost. But she is here. And she has already become more than I could have imagined. She is strong, determined, creative, expressive, affectionate, opinionated. When I would sit in the pumping station at the hospital, the nurses suggested I visualize my baby and think of something relaxing. I would try to picture Morgan as a toddler. I would imagine holding her hand and walking with her. It was hard to envision that future, especially when we didn’t know what was wrong. But now when I hold her hand and kiss those little scars, my heart is full of love and hope and gratitude. Morgan knows her scars mean the doctors fixed her. Someday I’ll tell her the whole story. My hope for her as she grows is that when she sees her scars, she won’t see flaws. I hope she’ll see them and know she got to live. That she was an answer to prayers and faith. That she was, and becomes more so every day, a beautiful gift.

Tuesday, July 12, 2011

Celebrity Sightings

Guess who the kids saw at the pool the other day?! John and Randy! And then Jeremy and I were at the movie theater and caught a glimpse of silly Brett! If you don't know to whom I am referring, then you must not be among the 246,307 [give or take a few hundred thousand] avid fans of Kid History. John, Randy, and silly Brett enjoy star status at our house. The kids have watched each Kid History episode untold numbers of times and have their fair share of favorite quotes. Among the ones I hear most often:

"Don't punch...our...car."
"I'm going to kick you in the head!"
"F-A-C-T!"
"I'm in so much twouble."
"Behave! I've had a...stressful day."
"Do you want to go on a hike?" "OkayI'llgogetmybags!"
"I'm going to eat some yellow grapes?"
"BUT...!"
"I don't want to have to tell you again!"

In truth, I hear much more than this. And, frankly, I've grown tired of requests to watch the episodes so many times. Nevertheless, it's not every day you get to see someone who's [almost] famous.


Friday, July 8, 2011

Sibling Revelry

I love my kids for lots of reasons. They're pretty great. Here's one big reason: they treat each other well. They are friends. Sure, they tease and irritate one another on a regular basis, but for the most part they care for and about each other.

Caleb spent last week at scout camp. It was his first time away for more than a night. I knew it would feel strange to have him gone and that his absence would leave a little hole. He is, after all, nearly the same size as me and eats about twice as much as the rest of us. What I wasn't prepared for was how his being gone would affect his siblings. Marissa in particular was a lost cause. The first couple of days were the worst for her. When she explained her rocky spirits to me, that she just missed her brother, I told her it was normal for her to feel sad since he'd been her friend since the day she was born. She tearfully told me how bored she was without him and how he takes care of her. I suggested she could write him a letter since Jeremy would head up to camp later in the week. This she did, and it was one of the sweetest things. It's one I'll hold on to for a while. [It'll make excellent evidence when they think they hate each other that they don't really.]

Caleb survived camp in one piece and came home to hugs and squeals of joy. I think the kids were a little bashful about the emotion they felt to see each other again. And now they're back to the teasing and the irritating ... and the caring that makes me love them even more.