Hi everyone, Lisa and I have decided that a Blog would be a great way to let all our friends and family know how our little girl is progressing in her first few tough days, weeks and months.
This is Olivia Grace Earp's story and we would love you to enjoy the highs with us and keep her in your thoughts during the lows.
I apologise for the rambling nature and somewhat thrown together appearance of the Blog but I don't have much time at the moment!
********You need to read from the bottom up with Blogs so the newest post is always at the top. Look to the right of the page and click on "Olivia's Story Post Archive" for the earlier posts***********
We are proudly supporting the Cots for Tots appeal to raise £1 million for vital equipment at St Michael's Neonatal Intensive Care Unit. Please have a look at the website and donate a few pounds if you can.
James and Lisa xx
Sunday, 30 January 2011
Day 13- The walls are closing in!
Olivia had another good day today and we put her first baby grow on, the stub of her umbilical cord dropped off and we had a visit from Lisa's mum and my dad and his wife. The baby grow isn't allowed to cover her legs as she has a long line that gos in to her leg just above her ankle that delivers her fluids.
After such fast progress these last few days have been so frustrating, she is settled and seems happy but because her aspirate levels are still up one day down the next she is still nill by mouth. The surgeons notes from the round this morning were very to the point but didn't really do much to inspire us...- "High aspirates-Plan of action- Nill by mouth." She produced 84mls in total yesterday which was her highest for a good five days, they were low whilst we were there today but might well be back up again by the morning.
The days feel like they are beginning to merge together now which is not a good sign, when you are sitting in the ward there is very little stimulation apart from the beeping of the machines and the odd cry from a baby. There are no outside windows in the room where we are so it becomes hard to keep track of time without checking your phone every so often (no watches allowed) and cabin fever is starting to set in. I'm sure when the feeds start and Olivia starts to spend more time awake everything will change.
New week tomorrow and we have everything crossed for her first feed so we can start to think about a few weeks time when she will be home. It's not like a broken bone where you have a date when everything should be back to normal by, there are lots of what ifs and maybes with gastroschisis.
Night all .
James xx

No comments:
Post a Comment