Nicolas Stein & Family: PICU

Sunday, February 21, 2010

PICU

Over the weekend Nicolas tried his best to recover but last night we had to turn his oxygen up to 2 1/2 liters and earlier today he had a fever...so we called his doctor and asked him to run some tests to determine if he was the same as when we left Lutheran Hospital or worse...We went to Parkview North and they did an x-ray and blood work....We found out pretty quickly that he has a new infection in his lungs and his white blood cell count is really high....After hearing this we went home and grabbed our bags and headed for Parkview Main hospital. We were admitted to the Ped's Intensive Care Unit...when we arrived they had to raise his oxygen to 4 liters...Now they have put him on bi-pap at 80%...It helps force the oxygen in there a little better...they are currently trying to do his IV...which is always fun...

This is all I know at this point. There are no phones in the PICU so I will try to update the blog as often as possible. Please prayer for our little guy!

Thank you!

Felisa

1 comment:

Jessica said...: I know you don't know me but I am a friend of Kimra's and just wanted to drop a quick note letting you know I am praying for your sweet Nico. I hope he gets better very soon!; February 21, 2010 at 8:55 PM

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If this is your first time reading our blog, here are a few things you may need to know...

This blog page is dedicated to informing our loved ones about our little Nicolas. It all began February 19th 2008. He was born a mere 6 lbs. 2 oz. and within 3 days dropped to 5 lbs. 8 oz. Initially Nicolas was diagnosed with Failure to Thrive and Reflux along with aspirating. He had a surgery at 7 weeks old to correct the reflux. They added a feeding tube at that time to prevent aspirating and improve weight gain as well. Once we checked out of Parkview North we began to see many specialists at Riley Children's Hospital in Indianapolis. After a few trips to Riley and several EEG's later he was diagnosed with Infantile Spasms...something he had been going through since 3 weeks old but was not diagnosed with until he was 6 months old. To try to rid Nicolas of these seizures, Jake and I gave him an inner muscular shot of a hormone steroid called ACTH. This medication dramatically improved his spasms to less than 1 a day. Before that, he would have 8-10 spasms a day. Due to the ACTH medication his immune system was affected and won't be back to normal until June of 2009. As of December 2008, Nicolas' MRI reported that he has a moderate thinning of the white matter that surrounds his brain which attributes to his delays in development. Doctors feel that all of Nicolas' symptoms are due to an underlying cause. Nicolas has gone through a great deal of tests in search of a cause and they have yet to determine what it is. Today Nicolas' weight and height are lining up with growth charts and his seizures are few. Through all of this, you wouldn't think anything has changed for our family. Not that this doesn't weigh heavy on us...it is challenging being patient with medical professionals and with a diagnosis. But through it all...we are so glad God gave him to us! We think he is incredible and love him dearly! With that I leave you this...read our blog so that you too can know more about Nicolas and our journey with him. Continue to pray for our family! Love, The Steins