The Ins and Outs of a Colonoscopy March 9, 2010
How do you prepare a five-year-old child for a colonoscopy? You don’t say, “Sweetie, the doctor needs to check your colon for growths, bleeding, or other irregularities. He will sedate you through an IV and stick a thin, flexible probe up your rectum so he can take pictures and biopsies. In order for him to do this, your colon needs to be completely clean, so Mommy and Daddy will deprive you of food for more than 48 hours. You can only have clear liquids, gelatin, and a limited number of popsicle flavors during that time. Oh, and you’ll also have to drink an over-the-counter laxative every two hours until your bowel movements are runny and clear. Okay?”
No. Instead, you say, “Sweetie, the doctor wants to take pictures of the inside of your tummy. We want him to be able to see everything, so your tummy has to be clean. It can’t have food in it. This weekend, you get to have special things like all the juice you want, popsicles, and jello! We’ll mix a special medicine into your juice to help you go potty. On Monday, the doctor will help you fall asleep so he can take pictures, and then we’ll go home and you can eat! Okay?”
The King and I bore the burden of knowledge for more than a week without telling our daughter. We wondered how she’d take it. I, for one, am grateful for a husband who took Butterfly aside on Saturday morning, cuddled her in his lap, and gently relayed the news to her. From her reaction, you’d think he’d offered her a trip to Disney World.
GG, the King’s mother, came to take Ladybug away for two nights. Without her sister’s competition for attention, Butterfly thoroughly enjoyed her two full days of having Daddy, Mommy, and Nana (my amazing Queen Mother!) all to herself, complete with new activity books, food coloring to mix into shaving cream, a new movie, a fresh box of colored chalk, and plenty of one-on-one time with each of us in turn. She drank her Miralax-laced juice like a champ, handled the resulting potty trips with grace, and suffered through a few bites of jello and sips of broth. Only on Sunday evening did she begin to complain of an aching belly.
By the time we made it to the hospital on Monday morning for our 8:30 check-in, our girl was puny. She rarely spoke, grew listless, and fell asleep several times as we waited in our little corner of what eventually became the recovery room, along with five other children getting upper GI scopes. One by one, the kids went away, got their IVs, and returned, only to leave again on their rolling beds for their procedures. A kind nurse came to give and get information, noted Butterfly’s condition, and quickly ordered fluids for her IV. The King carried her back for access, and later he reported that once her beloved Mickey Mouse got his IV, she took hers well. Apparently, the “magic cream” they rubbed at the site made the needle stick painless.
The fluids perked her up a little; she watched the Disney Channel while we waited for her turn. Nothing prepares you for witnessing powerful drugs put your little one to sleep. Even so, Butterfly (and her parents) did well. After the brief procedure, the doctor (whom I’ll call “Dr. GI”) spoke with the King and me, telling us about his findings. Unfortunately, Butterfly has some form of colitis. We are waiting for results from the biopsies Dr. GI took, which will help him determine between ulcerative colitis or Crohn’s Disease. He thinks colitis is the most likely diagnosis, which involves less of the digestive system than Crohn’s.
We were all surprised, considering Butterfly’s healthy weight, eating habits, and active lifestyle. Dr. GI said the lining of her colon bleeds easily and sloughs off. We saw pictures, and the problem is obvious. Basically, this is worse than we expected but not as bad as it could be. Medication can help control the chronic condition, and she will likely have a thriving adulthood. With good treatment, Butterfly can avoid any complications from the disease. I know enough about childhood afflictions to be grateful for something treatable.
The King and I are still trying to process what we learned. Of course, our consult with Dr. GI once the results come back will help. For now, we enjoy watching Butterfly as she enjoys life—creating her artwork, making “soup” outdoors from various nature items, playing with friends, telling us about her days at school, and aggravating her little sister. For now, we live.
So much of this reminds me of Rebecca’s heart procedure when she was four. Hang tough, Your Majesty! It sounds like you’re in good hands.
There’s an ache inside because I can’t transfer Butterfly’s problems to myself and bear them for her. It is the same for grandchildren as it is for children and doesn’t stop just because they grow up. I guess that is what love is all about. God has many lessons for us in life. May we learn them well.