Thursday, June 19, 2014

Day 7

The day started early and kicked off into activity.  His entire team assembled in his room, and each member gave their quick assessment and updates, addressing things like the blood clots and the ulcer, and helped us get a basic idea of how we are going to spend our time here.  These guys are exceptional, and it's clear why this place is perhaps the best in the state.  They are personable and fun, but very serious, thoughtful, thorough, skilled and focused.

Steve did two OT sessions today, and was just beginning his PT evaluation when he was called to surgery to insert the ICF.  This is essentially a filter in the vein just below the kidneys, and it catches a clot if it gets dislodged.  He has to lay close to flat for at least 4 hours following the procedure, and tomorrow he will get a full day of therapy in.

The dietitian came by and helped identify the best group of foods that he can get down for now, and anticipates a return to a regular diet by somewhere around Monday or Tuesday.  He gets more down at each meal, though still extremely painful.  The more he can eat, the less light headed he feels, and the more energy he can exert in his therapy sessions.

The kids came again this afternoon.  They received some legos in the mail from my cousin (thank you!!), and they brought them to Dad's room.  They have put their legos together and hung out with Dad.  It feels kind of normal-ish.  The kids finally asked me what his actual injury was, and we were able to talk about it.  They thought it was crazy and funny that Dad had metal and screws in his back!  I think they are processing each piece of information really well.

Steve told me to tell you all that your encouragement has been very important to him.  Taking the time to write those words has truly meant the world--that you heard, understood and cared.  Your prayers have bolstered us, and we truly believe are keeping us intact.  His world is pretty small still, so we are still not ready for visitors other than family and a few of our particular family friends.  But hearing your comments and email is invaluable.  To make sure he hears them, send them through me:  jennyearle <at> mac.com.  I will make sure he gets them.

Continue to pray -- your prayers are powerful!  Know that, as we are able, we are praying for many of you and the struggles you are going through at the same time.  It is our joy and privilege to do so as we are able.

2 comments:

  1. Jason thinks you should slip him a Newcastle when the dietician isn't looking.

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  2. They did ask him about his drinking habits... I just assumed a Newcastle would be worked into his regimen.

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