the scoop

"We are what we repeatedly do. Excellence, then, is not an act, but a habit." ~Aristotle

Saturday, October 24, 2015

Even Less Sugar: Caregiving Day One: Homecoming

I am not complaining. All of the things worked out fine, and we are fine, and Ian is home. I just wanted to give you a glimpse.

Yesterday: Laundry. Making the hospital bed that's in the living room. Potty chair and wheel chairs are ready to go. Bath chair arrives (thanks, friend!).

Mom meets me at the rehab center to get Ian. This round, I'm giving two types of antibiotics at home. One requires 4 syringes (2 saline, 1 heprin, 1 med, which needs to be kept cold and removed from the fridge 30 minutes prior). The other requires a very slow push, so it uses a giant syringe and a motorized pump. I receive a demonstration before leaving the hospital.
Freedom60 Pump

At 1:30 p, the school calls: Ezra is having "difficult bathroom issues" and needs to be picked up. We wheel Ian and his walker to the car, and with some difficulty load him up. Then we head to the school and get Ezra, who is "uncomfortable" but well enough. We cram in and head home. The home health nurse calls to say she'll be at the house around 5p.

IV medicine is due at 4. It won't be delivered till 4:30p ... okay. There's wiggle room. We're supposed to wait for the nurse to arrive to do the first home dosage.

The meds show at 5p. Still okay. I unpack the refrigerated box and bag of boxes of bags and meds and supplies and organize them a bit.  I realize: no magic pump.

Maybe the nurse brings it with her? Since I haven't been "checked off" on using it?

I should have known better, based on last time: meds are one folks, care is another.

Nurse shows at 6p (we're now at 2 hrs past due): no pump.

She calls, they're "sending it out," which means we'll have it by 9p. She sticks around for the meds I CAN do, and we do some math:

The antibiotics are on an 8-hour schedule. They are now staggered, 3 hours apart, and both have started later than the schedule. This means we need to fuss with the dosing times, using that aforementioned wiggle room to get them lined up together and properly spaced. It looks like this: (C and V being the two types; remember that "V" uses the pump, and therefore takes 1.5 hrs to run, followed up by another 2 syringes -- saline and heprin)

6p  C
9p  V (I want to sleep now, but I have to wait 1.5 hr for the pump to be done and do the other 2 syringes. Also, the second home-health nurse is here.)
-potty break for Ian somewhere around midnight-
2a  C (yup, this is not a pleasant wake-up)
-somewhere here, in a haze, is another bathroom trip. I think.
5a  V (wow, it's amazing what a dope I am at this hour, after a few hours of semi-sleep on a squishy couch. I manage to start the pump and set my alarm, fall asleep, get back up and disconnect, go back to bed, start to fall asleep, only to realize I forgot the 2 follow-up syringes. Back to sleep at 7.)
11a C (nurse is here! just to be sure I've got this. And I do ... although this is the easy one)
12p V (like a boss. Is it bedtime yet?)
7p C/V (they're both together now! yay! but we're not done fussing yet ...)
3a C/V (yup, that sucks - I'll either need to go back to bed for an hour or stay up till 430 ...)
10a C/V
5p C/V
12p C/V
8a C/V (the golden hour! now we can go back to the schedule we had at the hospital, 8 4 and 12. Much more manageable).

It's not that any of the things are difficult, or particularly stressful (although being apprehensive about being 5 hours late on a dosage was getting there) -- I've gotten "over" my extreme paranoia about screwing up the sterilization and antibiotic administration -- it's that all of these things are swirling around in my brain. They are all things to be considered and done, and that's outside the slow, arduous trips to the bathroom, the pill regimen, meals, kids, general house-type things .... and starting this week, the cadre of therapists who will be calling (phone calls! blech!) to arrange -- and then showing up to do -- speech, occupational and physical therapy.

Okay: maybe I'm whining. Just a little.

Monday, October 19, 2015

A Little Sugar: Sweet Times and Home Sweet Home

So, this happened:


On Saturday, after a full day's rest and a bit of administrative generosity, Ian got to visit with buddies from his Navy pilot days: Bluetails VAW-121 descended on a local restaurant to swap inappropriate stories and show their appreciation for "Rev." It was a MAGICAL night ... for Ian, 1. to be out of the hospital after two months straight, 2. to reconnect with brother-like-guys he hasn't seen in 10 years, 3. to exercise his brain with good memories and conversation. For me, it was like no time had passed ... it felt like a typical squadron function. My non-social self was completely at ease with the old crew, and it felt warm and fuzzy. No pity, just encouragement. It was like Normal Town for a few hours. (BTW, I had nothing to do with planning the event other than to get Ian dressed and to the restaurant. Thanks to all who coordinated this special night, and went out of their way to attend.)

You DON'T wanna know what was so funny.
And as if Saturday didn't give us enough of a much-needed high, today we got the news:

Ian comes home Friday.

I'm taking a risk, putting it out there in print this soon -- as I've noted before, things change, we take steps backward, drama unfolds. But I feel pretty good about this impending jailbreak.

What this means: Ian will receive in-home therapy from several specialists, likely followed by out-patient rehab. He will sleep on the 1st floor until he is strong and confident on the stairs. He will, of course, be open to visitors, if they are cootie free and have checked with me.

I am the wizard. The gatekeeper. The troll. Dr. David Banner ("You won't like me when I'm angry"). Get your flu shot, keep your germies at home, and do not "stop by" or "pop in" unannounced (this goes for family and clergy and the President, if he is so inclined); remember, his bed will be feet from the door -- no chance of your arrival not waking him. A call, email, Facebook message or text will let me protect his rest, his family time, and my sanity.

Lots more hard work to do. New phase, new challenges. But there has been triumph.


Thursday, October 8, 2015

Even Less Sugar: Rehabulous

weaving cones in a walker. like a boss.
First week of rehab is in the can. 

It's quite an adjustment go to from the buzz of the ICU floor, with much staff and sterile and beeping and always poised for the next specialist's visit to a chill, quiet, open hallway, no monitors attached. It might seem like a big relief, but it takes (me) a few days to breathe easy and not worry that he's not receiving enough medical attention. 

He's close to home! Yay! That's a fantastic, fabulous thing. Except it does raise some questions and some guilt: how much time should I/do I need to spend at the hospital with him? He's working hard ... does he need/want a cheerleader in his therapy sessions? Shall I wait for him to be done and then come to see him? If I'm not here every day, does that mean I don't care? (obviously not, but that's where the guilt comes in). Does a "pop in" visit "count" or should I stay for a few hours? How often should I bring the kids in with me? 

I was disappointed two days ago ... I watched him struggle with his tremor. He was pale. He said nonsensical things... he was too tired mentally to converse in a "meaningful" way. He was very cold, in a very warm room, and several coughs led to a raging headache.

It was depressing. I couldn't bring myself to come in yesterday. 

I kept reminding myself: He did this before. He relearned to walk. At one point, he sat with drool hanging out of his mouth, unaware of it. This is not that. We'll get there ... Be patient.

rehab snuggles (it was PJ day at school)
Audrey makes eye contact. So feelings.













But then I'd think: Yes, but this time he's altered going into rehab. He's not 100% to start ... what is baseline now? Is "generally confused" going to be the way things are? Is he ever going to show interest or patience in the minutia of conversation? Have we transitioned from best friends to caregiver and patient?

What happens when he's released from rehab? That puts me back into nurse mode again. I am the one to determine "how he is" going forward. Pressure.

I spent most of a day arguing with myself, dealing with my own demons. 

Today I steeled myself to get over it and spend time with my partner, my friend, my love. 

I was rewarded with a More-Ian Ian. 

Yesterday I felt defeated and rotten. Today, we can do all things. 

It's different by the day, folks. This journey we're on ... it's a bumpy one.