Fiona started grabbing her stomach a little on Sunday. By Monday night she was having some obvious pain and it was pretty apparent that she was really constipated. This is not our first rodeo, so I went ahead and gave her 2 full caps of miralax back to back before bed and nothing happened. She was up throughout the night complaining that her tummy hurt.
The next morning I had to go to work but let her dad know what I had noticed. He said that she'd gone twice on Saturday and was surprised she was struggling so much. He went ahead and gave her miralax with every drink that she had, but still nothing came out. I picked her up around 3 and tried to feed her lunch, she was in so much pain that she was arching her back and screaming...I'd already left a message at the ped office, but hadn't heard anything back.
I got a call back around 5 and Dr E said to keep up with the miralax and just do clear liquids. If her pain was out of control we could try and enema or bring her to the ER, but otherwise just watch her. She was miserable and wouldn't play or really move so I decided to bring her to the ER at Children's Hospital in New Orleans. It was such a disaster experience!
First off we had to wait over 2 hours to even get into an exam room and then another 40min to see the doctor. The doctor came in, did a very brief exam and ordered an enema. The nurse came and gave it to her and after an hour we still had no results other than Fiona falling asleep after screaming bloody murder. The doctor then decided that she would do an exam, and tried to break up the poop. Still nothing happened, but since Fi was sleeping she said she was fine to go home.
Well I don't think she was very comfortable at all, she was very shaky and on the car ride home she started projectile vomiting. I immediately called the on call ped who basically said, not my problem call the ER back they just saw her.
The ER was no help either and just said she was vomiting because of the pressure in her stomach and was fine to wait until morning and to follow up with her doctors in the morning. So I woke up 1st thing and called Dr E's and Dr C's offices. Dr E's office called and said it was a GI issue and left a message with Jeannine at Dr F's (our GI at Tulane). She called back and said to do another enema and a clean out. Fi ended up sleeping most of the day so we got a late start. After 5 doses of miralax, and a second failed enema Fiona began vomiting again. At that point I was really getting concerned so I brought her to the Tulane Pediatric ER.
We had to wait maybe a 1/2 hour, but they were busier than I've ever seen and were much nicer about the wait. They immediately said that they were going to make her feel better before sending us home which was really a relief. In typical Fiona fashion as we're waiting to see the doctor she pees (for the 1st time all day) soaking her outfit and the bed. When the doctor came in and saw, she'd also pooped a little he said that it was a good sign and that we were likely headed in the right direction he then gave me the option to have her admitted and do a clean out with Go-lytely using and NG tube or go home.
After thinking about it and discussing it with her dad I asked if we could stay a little while and see how she did before deciding. Well luckily Fi's body made the decision for us, she started screaming and freaking out and I was thinking, I guess we'll be staying, but amazingly she finally pooped, and was definitely feeling better after. So we decided to go home.
Today she woke up and has been a little cranky but she's finally back on track. For the first time in days she's been running around, dancing, jumping and best of all smiling. Her tummy is still bothering her a little, but overall she's a million times better. We've decided to take her back off of dairy for now since we really don't want to put her through this again.