Lidia – Day 7 – December 4, 2019

Physical Therapy

Brain surgery doesn’t slow down physical therapy.  We’ve attempted physical therapy every day.  But, today, was a first.  Today, with assistance, Lidia was able to stand.  

Note from author: Sorry the pictures are lame.  I could only take pictures from the front because if I took pictures from the back, Lidia would kill me, if you know what I mean.

Physical Therapy on Day 7

No Room In the Inn

This morning we were notified that we will be moving out of ICU to Acute Care.  This is a short move down the hall.  Lidia will have a private room with a private shower and toilet.  Instead of being 1 nurse for two patients, Lidia will be part of a group of 5 patients for 1 nurse.  

Unfortunately for Lidia, there are not any rooms available yet.  So she is still in her ICU room but is no longer considered Intensive Care.  

Stuffed Up Nose

Lidia is a nose breather when she sleeps.  It is against her character to breath out of her mouth.  I asked the nurses on staff overnight that if they wanted Lidia to be calm and sleep without fighting against high blood pressure, that they should figure out a way to keep her nose cleared from mucous. (I said snot, but wanted to be a little more sophisticated while writing this blog.) They went above and beyond to make sure Lidia was comfortable breathing out of her nose so that she could rest.

Officially out of Neuro Critical Care (ICU)

About 3 o’clock in the afternoon, Lidia was led out of the ICU to the Neuro Acute Care Unit.  Now that we are situated, I think we will find our routine.  We checked every 4 hours for a couple things.

  1. Bladder – We need to check every 4 hours if Lidia needs to relieve herself.  They do this with a portable sonogram machine.  (I have no idea what it is called, but that is what it reminds me of.) They are able to view the contents of her bladder non-evasively.  When she reaches a certain point, they do what is called a straight cath.  (Again, I have no idea if I’m saying this right)
  2. High blood pressure – They check her high blood pressure.  We are starting to learn Lidia signals for discomfort.  When she rubs her hand over her head and winces, she’s in pain.  When she wiggles her leg around or tries to adjust herself, she is feeling the need to relieve herself.

Neuro Acute Care

The biggest thing that I noticed on our first day with Neuro Acute Care Unit. 5+ PATIENTS TO 1 NURSE IS TO MUCH.  Each nurse has an assistant, but the assistant isn’t able to give meds, diagnose issues, etc.  However, I think this could be solved by having 1 or 2 floating nurses that aren’t assigned to any patient in particular but will go where they are needed.  We waited a little long to get Lidia relieved with a straight cath.  It took 3 hours for our night shift nurse to come and talk to us because she was busy with other patients.  Another thing that I noticed that was a big difference between Neuro Intensive Care and Neuro Acute Care is that there was always somebody asking if they could help the other nurses.  Somebody would come in and introduce themselves and state that they were helping our primary nurse.  

Lidia – Day 5 – December 2, 2019

Vending Machines

The vending machines take Apple Pay.  I can get vended food anytime I want using my debit card within my phone.  AWESOME!  I’ve been living off of Pop Tarts and Mountain Dew while Lidia is getting this great and nutritious concoction through a feeding tube.  I’m not sure which one is better. 😉

5 Star Accomodations

Or not.  I sleep on a couch that is about 4 feet wide.  My feet hang over the end while my neck is kinked on the other side.  It’s right below a window, so the cold air comes in makes me cold.  All this time, Lidia has the nice bed that adjusts to any way she wants, blankets, multiple pillows.  How come she get’s all the good stuff?  I’m joking. They always ask if there is anything that they can do for me.  I always respond that I’m fine and that she’s the one that needs to be taken care of. If she’s good, I’m good.

Cafateria

The food in the cafeteria isn’t bad.  After a while it gets old.  The same things over and over again.  I would have to say that the Chili Cheese Dog is my favorite.

Care Package

I received a care package from the guys at work.  Mountain Dew and some treats.  It kepts me away from the cafateria for a couple of meals.  I’m thankful for the guys at work, for their thoughts and prayers.

Poop

Lidia pooped for the first time since she’s been here.  Whoa!!

First Week In Video

Feel free to watch Lidia’s first week of recovery in video format.

Lidia – Day 4 – Sunday, December 1, 2019

Highlights

  1. Physical Therapy
  2. Taking a Breath
  3. All head tubes are out
  4. Patience

Physical Therapy

We had a 30 minutes therapy session today.  Not much to it.  They came in to get her moving.  Arms and legs.  Her left hand side is tight and they showed me how to help by stretching her calf by pulling the top of her foot towards her head slowly.  They also showed me how to hold her arm to stretch it out without pulling it out of it’s socket.

Taking a Breath

She had her breathing tube taken out today.  She is breathing 100% on her own.  She doesn’t even have supplemental oxygen.

All Head Tubes Are Out

The only tube we have now it the feeding tube.  I got bored and counted.  She has 65 staples.

Patience

I was hoping that maybe we would get her to talk now that she had her breathing tube taken out.  Unfortunately, she hasn’t spoken.  I don’t think it has really sunk in how fortunate we are to have Lidia still with us.  Also, I don’t think that it has sunk in at how much further we have to go.  I don’t see the light at the end of the tunnel yet.

This is the Snoqualmie Tunnel in the state of Washington.  The tunnel is part of an abandoned railroad and is 2.253 miles long.  While in the middle, you cannot see the ends of the tunnel.  Without a flashlight it is pitch black.  Lidia and I hiked this tunnel and took this picture on the weekend of International Geocaching Day in August of 2014.  We call this the Tunnel of Light.