Tessa Reed Shea's Documentary: Happy Birthday Mommy!

Saturday, July 23, 2011

Happy Birthday Mommy!

We celebrated Mommy's birthday yesterday so she decided to take the night off from helping me with the blog. Mommy and Daddy changed my feeding tube last night. The only part of that I don't like s taking off the tape. Sometimes it makes me so sad that I even cry:-( Here I am without my tube and Daddy is getting ready to put a new one back in....

Today Uncle John and Aunt Marie came to visit for Mommy's birthday. They stayed home to watch Brody and I so Mommy and Daddy could go out to lunch together. I tried not to give them any trouble and we had a good afternoon together. When Mommy and Daddy got home we cleaned up Brody's pool and he was able to splash around in it before dinner. I stayed inside with Daddy because it was too hot out for me. Then we enjoyed a yummy dinner and cake and all sang Happy Birthday to Mommy. Overall, I had a great day and I am laying on the couch with Daddy now. It's Mommy turn to watch me tonight and I will try and be a good girl!

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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.