Monday, March 9, 2009

Steps

It was another tough day in the NICU yesterday. The phrase "one step forward, two steps back" certainly applies. We went in to see Eli expecting that I'd get my turn to hold him again, only to see his ventilator settings had been increased significantly. This has been the trend over the past few days. I have tried not to worry but, of course, that is pretty difficult. Paul and I and our sister-in-law Melissa, who generously drove up from Philadelphia for the day to be with us, help around the house and see Eli, spoke to the doctor about Eli's condition. Concerned about Eli's breathing, the doctor ordered a chest X-ray, even though the one Eli had on Friday was completely normal.

This is one of those moments when you're reminded that, although medicine is a science, opinions can differ greatly when interpreting the data: The doctor thinks he sees another small collapse in the left lung, while the radiologist believes Eli has pneumonia. Although both scenarios sound scary, neither is an unusual development in preemies. Still, we'd like to think that our preemie could sail through without these complications--especially after having a string of trouble-free days.

To cover all bases, the doctor decided to treat both pneumonia and a collapsed lung, or atelectasis, as he called it, using a medical term we'd never heard before (this experience is an education in many ways). The staff started Eli on a course of antibiotics, which means he will have to have an IV put into one of his arms again and have that arm partially immobilized (understandably, he hates this). They also began doing physiotherapy on his chest again, tapping it firmly and repeatedly with a small rubber hammer to free up any mucus and reinflate his lung. The nurses told us we should start to see results almost immediately. We hope they're right.

2 comments:

Unknown said...

It's nice to read how family continues to help out (totally unsurprising, but it's comforting to know.) It's not so nice to read that Eli had another tough day but it sounds like you two are starting to get the rhythm of his process down, better able to contextualize his variations. He looks so strong and on it, it's hard to believe (from this end of the computer) that he has challenging days. Btw, I agree he has Paul's eyes (Steph may your son look more like you than my daughter looks like me, my vanity took quite a blow not seeing at least a bit of my genetic imprint in her corporeal dimensions.)

lots of love & hugs to you all
Abi

Unknown said...

Thanks Stephanie for the early morning blog comment. Dave and I were glad Paul called last night to tell us about Eli's day. Having a phone call AND the blog are a great combination for Dave and me, especially when Eli's world is somewhat harder. To see the words on the screen and get a chance to read and re-read them comforts. A big hug, Terry

P.S. This is my third arrempt to get my response up. Hope it works.