This is what started it all. November 15, 2010- I caught Katelyn napping on the floor. A very unusual
occurrence, so I thought I should take a picture. Little did I know what a journey this would take us on...

After two weeks of Katelyn taking a nap (or 5) every day, I took her into the pediatrician (Friday). This just wasn't her normal behavior. She never takes naps, and if she happened to, she wouldn't go to bed at night. But she was sleeping lots and still begging to go to bed at night. The doctor checked her for some normal things that would cause tiredness like anemia and a bladder infection. Both tests came back negative so the next day (Saturday) he send us to the lab for some blood work. Her results came back all negative- even for mono.
Monday she developed some new symptoms. I noticed when I got her out of the bathtub that she seemed a little wobbly. Unsteady on her feet. By the end of the day it had worsened. The next morning I was really alarmed when she was still doing it and her speech was not always clear. We immediately went to the doctor (Tuesday). He was quite concerned and sent us immediately for an MRI. I later found out he was looking for a brain tumor. SCARY! But the scan came back negative. So now we knew what was not going on, but not what it was. He sent us home while he did some searching and calling. Wednesday I talked with the doctor on the phone. He was still searching and wanted K to be seen at Primary Children's Hospital. So we made a plan to head up the next morning to the ER there.
December 4, Thursday morning we left. I picked up Jeff on the way at his office. Mid drive the doctor called me. (Jeff was driving.) Change of plans- go to admitting. OK. We had packed a few things in case we were admitted, but we weren't really prepared. Ryan (2 months old) was with us too.
We were admitted. The parade of doctors began. Pediatricians and Neurologists, all wanting to hear the same story again and again. It was decided that they would perform a lumbar puncture on my sweet Miss K. :( So she couldn't have anything to eat or drink since they would be putting her under. She dealt with the IV insertion amazingly well considering she had already had that done once for the MRI and had been poked for blood draws 3 times already. They did the procedure in her room as Jeff and I were in there too- pacing in the little corner that wasn't occupied by all the doctors and nurses. The results came back perfect.

Ryan can't bear to watch the LP. Neither can mom or dad.
Later that night Katelyn got all hooked up for an EEG to monitor her brain waves while she slept. The doctors were looking for seizures. She got an awesome hat and about a gazillion wires stuck to her head for the night. The next day the results look normal.

K sleeping soundly in her bed. Rice K
rispie treat still in hand.
Friday morning comes. The doctors are deciding whether to run more tests or not that require anesthesia. Katelyn is begging for food. They finally let her eat at 11am when they decide the plan for the day. A few more blood tests and more waiting. In the afternoon they convene and decide on a diagnosis.
Post-viral Cerebellitis-They put it together like this- she had a virus (no symptoms other than tiredness). The virus settled in her brain. Her body is fighting the virus, but also her brain. Swelling occurs in the cerebellum
impairing her motor skills (ataxia) and her speech. There is nothing they can do but let her body recover on its own. K should be better in 3 weeks. They will keep her another night for observation and we go home on Saturday.

Ethan and Erin come up for a visit. They think the playroom is the best and want to come back soon. Me- not so much. Two nights of no sleep with a 4-year-old and newborn are not so great.

K gets to ride in the wagon on the way out. She was so happy to leave!