Tessa Reed Shea's Documentary: Lost footage

Wednesday, November 30, 2011

Lost footage

Another "average" evening and day today. It's strange but I haven't had a medicine change in at least a week! Mommy and Daddy are usually updating the nurses each week with my medicine changes, so they have all been pleasantly surprised by that and my new room setup.

I was awake when Mommy and Daddy got home this evening so we had a quick dinner and clean-up. I needed lots of suctioning and Daddy gave me hyocyamine hoping that would help but I'm now giving my night nurse Heather a hard time. My fever is starting to creep back up so she was going to try some Motrin to see if that might help.

Mommy didn't get a chance to take any pictures today, but we did find some "lost footage" from last week. Brody woke up early and was giving me lots of love and attention. I love my big brother.

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My Story

I was born on January 18, 2011 and weighed 6lbs 14.5 oz and was 19.75" long. I was born with lots of fluid in me and no desire to suck or swallow. It wasn't until 12 hours after I was born that doctors started to worry about me. I had an MRI, CT scan and EEG and they discovered severe damage to the thalamus in my brain and diffuse white matter.

I spent a month at the Children's Hospital NICU and they sent me home with a nasal gastric (NG) tube because I still couldn't eat. I started to make a little progress drinking from a bottle at home (10 mls at a time) and then I got the flu and ended up back at the hospital.

It seemed like just after the flu I started arching much more than I had before and lost all desire to want to eat with a bottle. My arching episodes got much worse and Mommy and Daddy thought I had reflux or maybe a stomach ulcer from my NG tube. We scheduled surgery for a stomach feeding tube (G-tube), but ended up at the emergency room because I was arching so much and started to have trouble breathing.

When we checked into the hospital for the 3rd time, they gave me morphine to see if it would take away any pain I might be having from my NG tube. When that didn't stop my arching, they knew something else was wrong. They hooked me up to an EEG and found out that I was have lots of seizures, abnormal brain activity and something called hypsarrhythmia.

The doctors left the EEG on for several days to study my brain activity and my brain activity was something most doctors at the hospital don't see very often. That is when they diagnosed me with Ohtahara Syndrome and also a form of West Syndrome. The seizures are a side effect from my brain injury and my prognosis is not very good. Mommy and Daddy from the advice of some amazing doctors, have decided to bring me home to spend time with my family and experience as much love as I possible can.