One Week - Going Home

After 7 nights sleeping 💤 in the hospital it looks like we are going home today. Exciting! Willie has done really well making great progress towards healing every day. To me, it seems longer with all the sleepless nights of interruptions for medications at 10pm, 12am, 2am, and 6am, peppered with more interruptions for blood 🩸 pressure, temp, fixing leaky wounds, and call button needs. On the good side, we’ve had all that we need and the nursing care has been really good.

Yesterday they did an xray and blood test to make sure all is well. We will be task trained on how to change feeding tube liquid nutrition and what to eat. He is currently in a “full liquid” diet mode. Here is something’s he can eat while he is on that for the next several weeks until he can move to “soft foods”.

Today as we are patiently waiting to be discharged and talk to the doctor it’s been a different morning from the last 2. Normally between 7am and 8am which is shift change we have about 5 different people including Dr Loewen come in to do various things like bring food, blood pressure, shift change info’s and more. Today it’s been pretty quiet for a change. They finally brought in his breakfast at 8:45am. He’s already had 3 cups of coffee and wondering why he’s so shaky.

it was a beautiful sunrise this morning so we know it’s going to be a great day to go home.

Yesterday we had several visitors. It was nice to see everyone and he tolerated it well. He and I have been showered with some very thoughtful gifts which are very much appreciated.

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