Monday, September 25, 2023

Handwork...

I am now three quarters of the way through my chemotherapy, am climbing out of some rough days after my last treatment, and I am starting to feel some new motivation.  

I'm at a place I couldn't even imagine being just a couple of weeks ago.  On my good days I do fairly normal things, am sometimes out around people (though I do have to be smart about that with a compromised immune system), looking perfectly fine...   Halfway through a chemo cycle, if you didn't know I'd had chemo 10 days prior, you wouldn't know!   That said, I have lacked any real motivation for getting back to a lot that is normal for me.  In this post, I'm referring to hobbies I used to enjoy.  I see them sitting there and I want to want to do them, but I have lacked the motivation to actually do them.  Things like crafting, embroidery, cross stitch, slow drawing (if you don't know what that is, think of it as purposeful doodling)...  

But something seems to be changing inside me, and I am so thankful for it.  I've even begun to consider taking up sewing again - like maybe clothing.  I haven't sewn clothing since...   Wow - how long has it been?   I made some maternity clothes 29 years ago.  And I made some flannel pajamas for our boys when they were little.  Okay, I've sewn here and there over the years.   Craft projects, even home projects have seen me sitting at the sewing machine.  While it was over a decade ago, youngest son would benefit each semester from my sewing skills when he needed a costume (usually something adapted from the thrift store) for a high school drama he was in.  My sewing machine has always been fairly handy, but I don't think I've sewn an article of clothing in 20 - 25 years.  

I know what has piqued my interest.   Greg has recently posted some old pictures to a family Facebook group, and in two pictures I recognized I'm wearing things I made when I was young.  In fact...  just for fun, here is a scan of a newspaper clipping of young me sewing a 4-H project.  Or maybe I was just posing for the 4-H Fair supplement for the local paper:  


So...  I provide this as proof that I used to be a sewer.  Or maybe the better word is sewist.  A maker of garments.  Seeing pictures of things I had made (and me wearing them) made me think of other pieces of clothing I've made in years' past.  These pictures and memories sparked something inside of me.

Okay...  I'm not sure about getting back to sewing clothing for sure.  I'm just dreaming at the moment.  But dreaming feels good.  And a little doing recently has done me good.



It's funny what can come along and push us out of our inertia when we are struggling with motivation.  With cooler weather right around the corner I've started looking at my clothes to see what still fits me at this point, what can take me through fall and winter, and what might benefit from some simple altering.  I found a few tops that, by altering the neckline, should be very comfortable and decent looking for me to wear.  And I'm so surprised at what has happened.  Simply putting thread to needle, and doing the easiest of clothing alterations has inspired me to want to do more handwork.  

It led me to pick up another needle and thread and start working on my Quaker Sampler again.  


I don't know how many times I can show a picture of this sampler in progress before losing all credibility that I'll ever finish it.  But I don't care.  I'm back at it for now.

And I've even gotten some ideas for hand-stitched Christmas ornaments - some "scrappy" slow-stitching kind of projects. 


This is actually a fairly ambitious project (for me), and if I'm being completely honest, I'm a tiny bit scared I'll not follow through.  Wish me well that I have enough gumption to get it started, let alone finished.   

I am so relieved to be feeling motivated again to play with fabric and thread.  To just be dreaming of things I want to make is quite the improvement.

There is nothing wrong with setting aside activities, even abandoning them completely as life changes, but that's not what I wanted.  I have wanted for so long to get back to making things - really, since our move nearly two years ago I haven't been overly motivated to do handcrafts.  And this year, with all the cancer business, my zeal for "making" has just been completely zapped.   I'm feeling relieved that something seems to have changed in me.   

I'm curious...  What do you do when you find your motivation for favorite activities waning?  

 

Saturday, September 16, 2023

Green Beans, Sausage and Potatoes...

On a much lighter note than recent previous posts, I'm shifting gears to share (mostly recording here for myself so I don't lose it) a new-to-me dish and recipe:  Green Beans, Potatoes and Sausage.   

A super easy recipe, that harkens back to simpler, heartier times, this is actually a very old dish.  I imagine my own mother made it and served it, and I'm sure I would not have thought this was good as child.  In fact, it was only when a friend made it for us recently that I found out how delicious it is.  I've made it twice now - with mixed results.

My best version of this was made with fresh green beans.  Many people use canned green beans, but when I tried them they cooked down too quickly, and when I reheated it, the green beans were practically mush.  While I didn't cook the canned beans nearly as long as I cooked the fresh green beans, I may have still cooked them too long.

There are many variations of this recipe online, and this one is very simple.  It can be made bolder by adding bacon, or using bacon drippings, and by using some other spices (I'm thinking of trying a shake of Creole spice mix next time).

I cooked the ingredients separately, and add them all together after the beans are cooked since the separate ingredients will take different times to cook.  Most recipes I've seen online do not do this, so I'm open to thoughts and suggestions about this.  I've also seen a sheet pan recipe that looks like it might just be amazing.  But for now, I offer up:

Green Beans, Potatoes and Sausage



Ingredients:

Fresh Green Beans (as much as you want to make)
Potatoes, cut up into bite-size pieces  (I think any type will do)
Rope sausage, sliced or cut in chunky bite-sized pieces  
         (I used Hillshire Farm Smoked Sausage)
Chicken Stock (at least a quart)
Onion, chopped
Salt
Pepper
Garlic Powder (can also use fresh, minced garlic)
Any other favorite seasonings, to taste

Wash and cut fresh green beans.  Heat beans up in a pot of water or chicken stock (or a combination of both) and cook until beans are tender.  Depending on the type of green bean used, this can take anywhere from 30 minutes to an hour or more.  If using canned green beans skip cooking the beans ahead of time. 

While beans are cooking, saute slices of sausage along with chopped onion until the sausage is heated through and browned.  Set aside.

About 30 minutes before the beans should be done, either boil or fry up the potato pieces (I boiled mine, but will saute them the next time) until tender.  Drain boiled potatoes and set aside.

Once the green beans are tender, add the seasonings along with the sausage and potatoes to the pot of green beans.  Cook until flavors meld, and the whole thing is hot. 

You can eat this like a stew by scooping out liquid with the beans, potatoes and sausage, or use a slotted spoon to dish onto a plate.  We've eaten this as a main dish (don't think I served anything else with it), and I've enjoyed the leftovers for as long as they've lasted.  The first batch (made with fresh green beans) I shared with a friend, I thought it was that good.    

I would be interested in reading in the comments any variations you may have made of this dish.  Also, I'd love to hear others' experience and suggestions you have for using canned or even frozen green beans.




Thursday, September 14, 2023

Part 4: Hospital Stay, Days Six and Seven...

I haven't really written about how my overall health (mental, emotional, and physical) suffered - especially during the second half of my week in the hospital.  



Because a few lymph nodes were removed from under both arms during my breast cancer surgery in June, the hospital placed arm bands on both wrists indicating that I was not to receive "sticks", nor have blood pressure taken via my arms.  There is currently debate about how important all this is in terms of the risk of developing lymphedema, but this hospital (at least in theory and signage) seems to subscribe to older standards in this.  At first thought, I appreciated it, but since both sides of me are potentially affected, it does sometimes present nurses and techs with a bit of conundrum - or so it seemed.  In the early part of my hospital stay nurses and technicians had need to stick me numerous times to get blood draws and to insert IV's.  In short order I became a veritable human pincushion.  Both arms, when IV's were attempted and failed, swelled at two different times early in the week.  This didn't appear to be lymphedema, but unwelcome fluid, nonetheless.  Two different days I remember each arm was wrapped up in warm blankets for hours to help reduce the swelling.  So many new experiences...  



To be clear, it's not the successful sticks that are all that problematic, but rather repeated misses.  And since a tourniquet is supposed to be avoided (again, under the old rules regarding lymphedema risk), there were a lot of misses or failed sticks.  It appeared to me the misses cause more bruising than the successful sticks.  Few seemed skilled at finding suitable veins without a tourniquet, though, so after two arm swelling incidents, they finally started calling in special technicians to do sticks with ultrasound.  That was a great improvement - both in finding veins, and in the pain of getting stuck. 

It was a little surprising, after all that, when a tech came in to insert an IV and she casually laid a rubber ribbon across my arm.  I spoke up that tourniquets were not be used, and she seemed confused about how to do what she needed to do.  Fortunately, my nurse was right there, too, and I asked, "Can I just require that from now on all sticks be done with the aid of ultrasound?"  I was told yes, so I made it my mission to speak up should someone pull a tourniquet out again, but it must have been put in my record, as I never had to actually do that.    

I'm not sure when the fluid retention started, but by Saturday my lower legs and feet were swelling to the point that when I was wearing shoes, they left an indentation on my feet - and that was just the beginning.  I was weighed a couple of times to try to track how much fluid was accumulating, and when the number went up, it was alarming.  X-rays were taken to see if there was any fluid around my heart and lungs. 
 



For someone who was well enough to go home on Wednesday, I began to accumulate quite a list of scary symptoms that no one seemed to be able to figure out what was causing them.

The point when my blood pressure soared to 200 systolic, may have been when I moaned,  "I've gotta get out of here before you guys kill me."  It came out totally as a reflex, and I realized immediately it was a terrible thing to say, but hoped that they took it to have been kind of made in jest.  I couldn't unsay it, but what was I to do?  I didn't really think they were going to kill me, but by the weekend, when I had been needlessly restricted to my bed and a recliner with alarms, I knew the restriction of movement was not what my rising blood pressure or fluid-filling body needed.  I needed to get out there.  I needed to get home and start moving normally.

At one point, it was suggested that if the swelling didn't subside they might need to restrict how much fluid I drank.  That just about undid me.   Between chemo and antibiotics, and now a diuretic and high blood pressure medicine, my mouth was dry as a bone.  And on top of all that they might have to restrict me from drinking fluids?!?!   At some point, for a day or so I starting to have some trouble breathing during the little bit of moving around I did do, and another x-ray was ordered.  

I've lost track of when my oxygen levels dipped, but I spent one night and part of the next day on oxygen before it resolved.  Thank goodness that didn't go on for too long, but the craziness of the situation seemed to change and sometimes compound daily as the week and weekend wore on.  


Back to my saga...

To top off my unhappy Saturday, after I had gotten somewhat settled into bed for the night, I found out the alarm on my bed had been tightened so that I couldn't even turn over without it going off.  And that's exactly what happened right after the nurse left the room.  How much could a person endure!?!  When the nurse came in to turn the alarm off, exasperated, I said I couldn't sleep this way.  I got out of bed, and going back and forth between bed and recliner,  I carried blankets and pillows to sleep on the recliner, venting my frustration the whole time.  In addition to not even being able to turn over in bed, some of my frustration at that point was also due to feelings I was having over the dissatisfying conversation I'd had earlier with the administrator.  To my nurse's credit, he remained kind and appeared patient, letting me vent. 

Sleeping in a hard vinyl recliner is not very easy to do, though, so I was exhausted come Sunday morning.  Even though I only had to endure one more day of this craziness, all I could see stretched ahead of me were hours upon hours of enduring this miserable alarm business.  

To add insult to injury, Sunday's lunch from the hospital kitchen was inedible.  Most of what I got from the kitchen all week was too dry to be considered good, but late in the week I discovered the cheeseburger was pretty decent.  So much for trying to make healthy choices.  Come the weekend, I decided that would just subsist on cheeseburgers on Saturday and Sunday.   But when I got a hocky puck of a hamburger on Sunday, I sent it back to the kitchen, and decided I was done with "room service".  I would live on Cheerios and cheese and crackers from the cancer floor kitchen for the next 24 hours if I had to.  What perfect timing when youngest son called shortly after that and asked if I was up for a visitor.  Yes!  Please!  And will you bring me a lunch, and a salad for supper?  He was a sight for sore eyes, when he arrived with food.

Now, I don't know when it happened, but at some point on Sunday I realized that someone had left the chair alarm unplugged from the recliner, and I wasn't about to point it out to anyone.  When my son was there, I took hold of my freedom and pulled a straight-backed chair up to my "tray table" and sat there like a human being while I ate.  A tech came into the room at some point when I was eating and was surprised to see me sitting where I was sitting (i.e. not on an alarm) and said something about it.  While I tried, even with the stress of the weekend to always treat everyone with respect, my patience was starting to wane by this time.  I said, "I have another person in the room with me.  Can I not be free to walk around in that case?"  I think I also said something about not knowing what the rules were anymore, and if I'm being completely honest, I might have said out loud, "I don't even care."  Honestly, I think the tech was confused herself at that point, and she let me be.  I enjoyed my meal, and the visit with my son in peace.

It was later that evening when I was alone again and had been in the recliner for several hours, and the night nurse came in that I noticed that my lower legs and feet had swollen to (what I thought were) frightening proportions.  I had been wearing some no-skid socks from home that had ribbing on them, and the ribbing indented my ankles to their normal skinny state, while the fluid swelled my lower legs and feet to look like they belonged to a freakish comic book character.   When I took the socks off, I told the nurse, "These are not my legs and feet!"  It might have been funny if it wasn't so disturbing.  She helped me prop my legs up on pillows, and I tried to wriggle my feet around just to see if moving them would help drain some fluid.

Having forsaken the bed alarm the night before, I slept again in the recliner on Sunday night. There was no venting this time.  I was already there and I just resigned myself to sleeping there.  I was told some time on Sunday evening that the supervisor of the administrator who had spoken to me on Saturday evening would come and visit with me on Monday morning.  While that was too late to do me any good, I said I would welcome her visit.  The problem was that in anticipating her visit, I couldn't sleep for thinking about it and what I wanted to say to her.  

It was mostly a sleepless night.  I repeatedly got up to go to the bathroom that night - setting off my alarm for the duration of my absence, only to have it continue to sound until I came back to the recliner and sat down (at which point the alarm would shut off).  Numerous times during the night, no one heard the alarm - or at least, no one came to shut it off - making the whole situation even more absurd.  It's a good thing I didn't actually need help.  After a few hours of trying to sleep, I developed another terrible headache - actually, nearly every morning and/or evening the second half of the week, I was experiencing bad headaches.  Was it my blood pressure?  Was it the emotional toll all of this was taking?  Was it the impossibly uncomfortable sleeping options?  I'm sure it was everything. 

Finally, in the still-dark hours of Monday morning, exhausted from no sleep, I knew I'd had enough of the craziness.   I'd had enough of worrying about my health growing worse as the weekend wore on.   As I sat there, in the dark, with a massive headache, looking at my swollen feet, I finally said to myself, "If this place cares more about their liability than they care about my health, I clearly have to take control of the situation".   I don't know if I called the nurse into my room, or if my alarm did when I got out of the recliner, but she was soon there watching me as I was (again, all by able-bodied myself) moving blankets and pillows now from the recliner to the couch.  The couch, while it was too short to lay stretched out on, was the only place I could lay down that didn't have an alarm.  I got a cold wet wash cloth from the bathroom to put on my head, and I tucked myself in as best I could on the hard vinyl and told the nurse,  "I'm done with the alarms.  I'm rejecting them and I'm going to try to get some sleep here on the couch."   



At first it seemed as if my nurse didn't quite know what to do.  I was so busy taking care of myself, I didn't even pay attention to whether she was in the room anymore.  And then, when I was all wrapped up and curled up on the couch, with a cold washcloth over one eye, and feeling like I might have just started to fall asleep, it seemed like she bent down close, and sounding like she was reading a list of what all I was risking if I fell, she told me I could suffer a concussion, bleeding into the brain, and I don't remember what else...   It all sounded dire, but I knew the risk was slim to none, and I told her I accepted the risks, and I held her harmless.  I did poke my head up to ask if they would continue giving me prescribed medicines (I only knew for sure that I was getting antibiotics at that point).  She assured me I would be given medicines.  I was then left to sleep for what felt like the most glorious, peaceful few hours of my whole time in the hospital.  I never saw that nurse again.  It makes me kind of sad because she was the nurse I had the first night of my hospital stay and then again on my last night, and I hated that it ended with her on what was probably a seriously unpleasant note from her perspective. 

I'm not sure what time it was when the next day's nurse came in.  I barely remember interacting with her early in her shift, but I think she came in early and left.   When I finally woke up the whole scene was very surreal.  It was extremely quiet outside my room - which was was weird because my room was right across from a juncture of two hallways and it was never quiet for very long.  It could have been my imagination, but it  felt like I was intentionally being left alone.  Was the word out to leave the crazy woman be?  Let her sleep?  Keep away from her?!?  I knew I hadn't been the least bit crazy, but I still wondered if I was being talked about.  And left alone.

While I'm sure it felt terrible to my nurse for her to end her shift with me on the couch, personally, considering what I had endured, I think I was a fairly pleasant and peaceful protestor.  All I did was declare I was done with the alarms and took matters into my own hands where I slept.  While it felt like kind of a big deal in the moment, it also felt like the only responsible to thing to do.  There was really nothing more to it than that.   

Still sleepy, I got up, opened the window shades, and sat in the recliner for a while taking in the peaceful, quiet morning - knowing I would be sprung at some point that day and as far as the staff was concerned the patient who'd lived in Room 4111 for the last week would just become history.  That also made me a little sad since most of the week I had been fairly cheerful, mostly pleasant, overall a downright decent person. 

It did make me wonder, though...  Could I have had this kind of peace if I'd declared my independence earlier?   I actually did try to on the Saturday that I fell.  My nurse, who was wanting to help me, thought I could refuse the alarms under the umbrella of "refusing treatment".  When she told me that, I happily declared that I refused them.  Shortly after that, she was told by her supervisor she was wrong for telling me that, and I guess my declaration of refusing the alarms went out the window at that point.

Anyway...  finally feeling fully awake, being completely able-bodied, I got a shower, got dressed, got packed, and was waiting when Greg came to pick me up around 10am.  

Shortly after he arrived, my quiet, ignored room suddenly became a hive of activity.  While doing all the last things that needed doing for me to be discharged, at one point I had in my room the discharging doctor (who I hadn't met before), a technician who had some imagining machine (I cannot remember what she was needing to get a picture of at that point in time), and two people from the home health care company who brought in a large box of the balls filled with antibiotic that we had to tote home.  It was quite the scene.  Greg told me later as he looked on from the couch, it was unbelievable that while one person was trying to take my blood pressure, another person was talking to me, asking me questions and having me sign papers.  The doctor, trying to listen to my breathing, at one point tapped me on the back of my shoulder and told me to stop talking when I tried to answer questions that were asked of me.  LOL  The ridiculousness of it all kind of made me happy.  It was as if I couldn't take any of it seriously anymore.  Or maybe I was just glad that it all meant I would be leaving soon.

With all that finally over, I was then told that the administrator who wanted to see me had finally gotten there and would soon come to my room.  Believing I would be leaving at any moment, I said I really didn't want to begin a conversation that we might not have time to finish.   At some point, though, she stopped in.  She was a friendly, approachable woman, and I while I didn't anticipate having enough time to talk in any meaningful way, I was actually glad to see her.  I don't know how she felt brave enough to show up without a police officer "friend", but I was thankful for it.

We ended up having plenty of time.  I told her much of what I had told the other administrator on Saturday night.  And she seemed more thoughtful and caring about what I had to say. The thing that seemed to have the most impact on her was my telling her that the night before, when I couldn't sleep, I was looking online at the hospital's Patient's Rights page, and I began to wonder if my patient's rights had possibly been violated by this computer-driven policy, in that when the staff was compelled to follow the instructions given by a computer, I instantly lost my voice in the discussion of my care.  I told her I felt like I had a voice with the nurse, but once the nurse was overridden by a decision made by a computer, and since everyone claimed to be at the mercy of the computer's decision, I no longer had a voice.  

She joined the chorus of all the hospital staff in saying that they are extremely frustrated by this policy.  That it takes away everyone's autonomy, and the nurses and their direct supervisors think it can cause more harm than good.  It certainly did in my case.  I mentioned that I would be interested in writing about my experience and submitting it, and she encouraged me to do so.  She believed it might be helpful as they continue to discus the policy.  I told her my first priority when I got home was to get some sleep, but I would write about my experience, and submit it.

These posts are a longer narrative of a shorter, more succinct, report I have written for the hospital.  I have to say, reliving the ordeal filled me with depression and sucked the life out me for a time.  My experience of spending a week in the hospital (for the reasons I was compelled to) took about two weeks to mentally and emotionally recover from.  

I'm better now, thankfully.  Scarred from the experience, but better.  

ETA:  My blood pressure was within a healthy range by the time I got home the same afternoon I came home (was taken by the home health care nurse), and even the swelling in my legs and feet were starting to resolve already that day.  In less than a week my legs and feet were completely normal.

For what it's worth, I walked out of the hospital on the Monday I was discharged (a week after walking in).  Walked the distance from the cancer floor to the elevators, held my own as I rode from the fourth floor to the first floor, walked all the way to the front doors, and out to where our car was parked a bit of a distance from the front door.  Figuring I would be told it was hospital policy for me to be wheeled out, I was actually planning on walking out on my own two feet in protest, so I was a tiny bit disappointed when the nurse told me it was my choice to walk or use a wheel chair.  

This same nurse gave me a big (and slightly lingering) hug after we loaded the car with all my stuff.  I was surprised.  Normally, they practically tip you out of the wheel chair into the car before they rush back into the hospital.  I received the hug (and gave back in kind) as a confirmation that I was a decent patient, and maybe read into it a sense of apology that I had had to endure such a terrible ending to a hard week.

It was not the people (especially nurses and technicians I encountered) that work at this hospital who were the problem in any way. They were mostly wonderful.  Kind and caring.   It was the system of allowing a computer to make a decision that impacted a patient's well being - on so many levels - that was the problem. 



Wednesday, September 13, 2023

Part 3: Hospital Stay, Day Five...

My friend, Dory, hearing I would be spending the weekend in the hospital, contacted me to see if I'd like a visit on Saturday.  Oh yes!  You'd better believe it! 

I got up with new purpose on Saturday, showered, put on normal clothes (including shoes), and waited for Dory's arrival.  I checked with my nurse to see if there was anywhere other than my room where we could meet.  Not that Dory wouldn't have been fine with meeting in my room, but I was ready to spread my wings and visit some other corner of the hospital after being given permission to do so the day before.   I was told there was a "Friends and Family waiting room" that we could use.  Great!  I met my friend at the elevator and we went to this little "kitchenette" room to spend an hour or so.  Dory brought us milkshakes (a heavenly treat after nearly a week of hospital food), and at some point, she broke out some cards and we started playing - what, I don't remember.  Thankful she had thought of cards, I was nearly giddy to be doing something - anything - so ordinary.

At some point in the visit, I decided to make a trip back to my room to get some things (one item being a cup of ice water for me).   On my way back to the room where Dory was waiting for me, I had to pass through two different sets of double doors.  As I approached the first set, a motion detector started two doors opening in opposite directions in front of me.  Now, I don't know if you've ever had this happen to you, but as I walked (maybe a little too quickly) the soft rubbery toe of my right shoe grabbed onto the highly waxed tile floor, pitching me slightly forward.  When this has happened to me before, I've sort of jerked my arms out a bit to keep my balance, and then a tad embarrassed, regained my footing and simply carried on. But this time, I suspect because of the opening doors ahead of me (and the one coming toward me that I needed to avoid), and maybe because my hands were full, and maybe because I was walking too fast and happy...  I fell.  To the floor.  On one knee, and possibly my posterior.  I don't remember exactly as I was up nearly as quickly as I went down.  But the nurses saw it and came running.  

While certainly embarrassed at my clumsiness, I didn't think it was a big deal.  I mentioned that I spilled some water and I think I even said, "I'll get some paper towels", to which a nurse replied, "We'll take care of it."  They were only concerned that I was okay.  I assured them I was fine, and thinking nothing more of it, I happily made my way back to my friend who was waiting for me to return.  I told her what happened, laughed off some of my embarrassment, and I think I was beginning to deal cards when my nurse and technician came into the room very somber.  They explained that they would have to report the fall, and check me over to make sure I wasn't hurt.  They communicated that they felt terrible about it, but it would mean that I would need to go back to my room.  And that I would have to have alarms turned on on my bed and recliner.  I'm still stunned remembering that moment.  I had just gotten freedom to leave my hospital room in some meaningful fashion, and the freedom was being snatched away over a stumble that could have happened to anybody!  I started to make the argument that controlling my fall (rather than tumbling into a moving door which would have surely injured me), and picking myself up as ably as I did was clearly evidence of my being able bodied.  It was my shoe that was the problem, not me.  The issue was so ridiculously obvious, I was having trouble taking it all seriously.  In disbelief, I even joked, "What are you going to do if I don't comply - kick me out?  Please do!"   I was just incredulous.  And heart broken.

Even though they felt sympathetic, and they knew the stumble had not been a reflection of my ability to walk, they had to comply with hospital policy.  This is the point where I learned that a patient's "fall risk" is a compilation of things, some of those things having little to nothing at all to do with any individual's actual fall risk factors.  In the end, determining a patient's "fall risk" is about statistics and liability.  Statistical factors, as well as real factors (of which I had none at that point) are entered into a computer and an algorithm takes the decision out of nurses' hands to assess an individual for his or her personal risk factors for falling.   Things like medicines and various signs of instability (these I can appreciate), age, and even sex are typed into the computer.   I have no idea if certain statistics are true, but even accepting for the sake of argument that say, statistically woman perhaps fall more than men (though without knowing why, the statistic has very little value), that statistic has nothing to do with me as an individual.  It has nothing to do with my personal "fall risk" and everything to with the hospital's liability risk. 

After Dory left, I sat in my room for a couple of hours on an alarm pad that would sound if I got up.  To say I was indignant would be an understatement.  As I stewed over the whole thing I became increasing angry over the stupidity and wrongness of the situation.  And not just for me.  I was incredulous that a hospital expects patients to trust the professionals it hires to care for them, but the same hospital will not trust those same professionals to asses a patient and make reasonable conclusions about something like this - after hours (in my case, DAYS) of observation of a patient.  Nurses that I had literally trusted with my life all week, were stripped of the ability to make a decision that would respect my actual abilities and mobility - that they could clearly see were fine.  That a hospital would adopt a policy to allow an algorithm to make such a decision and turn a trusted relationship into potentially an adversarial one was just ludicrous to me. 

This might be a good time to mention that on Monday night after my emergency surgery, and at least part of Tuesday, there was an alarm on my bed.  I was weak and on medicines and at times could barely keep my eyes open.  I was hooked up to various things, and I couldn't get up and walk anywhere without someone unhooking me from something attached to the wall (a heart monitor, I believe).  There was no thought during that time that the alarm was for anything other than my protection.  I didn't resent it.  I understood its purpose.

But once I was unhooked from the heart monitor, I demonstrated numerous times that I could take the IV pole to the bathroom and manage perfectly fine.  In fact, it wasn't until they took me off the heart monitor that I began to question the need for the bed alarm.  At that point, I had become strong enough, and the staff had had time to see that I was stable.  I don't remember asking more than once before the bed alarm was turned off for me.  The alarm wasn't an issue to me when it was needed, and it seemed to be an easy decision for them to remove it when I became stronger and it was no longer needed.

Anyway, after stewing about my new confinement for a couple of hours, I unplugged the chair alarm I had been resentfully sitting on and walked myself out to the nurses' station and asked if there was an actual human being I could speak to about the situation.  To be clear, these were my nurse and tech who felt bad about the whole thing, and who wished there was a way around the policy.  They appeared happy that I wanted to talk to someone higher up.  They said they would request this person come and talk with me.  With new purpose, I went back to my room to put some of my thoughts down on paper while I waited for this person to arrive.  A half hour or so later, I heard someone(s) coming into my room.  My back was to the door, but I began to greet my visitor(s) as I pushed my chair back from a little table I was sitting at.  Imagine my shock when, as I turned around, I saw a police officer standing in my room. Beside the police officer was the person who I was told would come to speak with me.  I don't remember what her title was, so here on out, she will be known as the administrator.

Now...  while I was incredulous to see the police officer, it only took me a few seconds to realize she was there in case some sort of protection was needed.  I guess.  Or was her intimidating presence the sole reason for her to be there?  The administrator referred to the police officer as "her friend" that she always brought along to this kind of meeting.  Feeling patronized that that was her explanation of a police officer's presence in my room, and I'm sure stifling an eyeroll, I concluded I just had to "be the adult" in this whole situation.  I stated that I was surprised to see a police officer, and said her presence made me nervous (my voice was now shaking a bit and I figured it was better to just be open about my discomfort), but in spite of that I pressed to explain my issue.  Actually, just before this, I asked the administrator who was a young woman and towered over me if we could both have a seat.  She hesitated, but when I sat down and motioned to the couch where she could sit, she did so - even though she didn't look like she really wanted to.  What I had moments before I envisioned as an opportunity to reason with someone in authority, and bring a little humanity into a situation that was being controlled by an impersonal policy and a computer algorithm, was suddenly feeling very unfriendly.  But I pressed on.

The administrator seemed nervous, too, from what I could tell.  I'm in no position to know how often a police officer is needed in a situation like this, but in my estimation her presence in the room was a complete negative in this case.  Afterwards I wondered, Could the officer not have been outside the door waiting for me to - do what, I don't know?!?  But just in case the administrator really did need her help.  Like if somehow this 64 year-old woman who is supposedly too weak or unstable to walk around freely, is strong enough to inflict harm on a nearly 6 ft tall athletically built young woman.  

I'm sorry.  It gets really hard for me to not get sarcastic as I recall all of this.

Interestingly, about 20 minutes in (though I have no idea, really, how much time had passed), the administrator evidently felt safe enough that she dismissed the police officer.  The atmosphere changed immediately.  I know I instantly relaxed, and the administrator appeared to let down some of her guard.  At some point, the charge nurse came in, and we actually had some friendly discussion amongst the three of us.   At some point, when we were in this more relaxed state, and I brought up issues of privacy - which I felt more keenly because I had a male nurse and tech that night, the administrator actually began to suggest "work arounds" to the problem.  Things that could give me some autonomy and privacy (for things like going to the bathroom, for crying out loud).  That I had to even ask for that in my able-bodied state troubles me - still.  While, on some level, I appreciated the suggested work-arounds, they really only made a mockery of the whole thing.  That they were offered, highlighted that there was a problem with the systematic, impersonal way in which patients are identified as fall risks.  In the moment, it felt like something, though.  But when I discovered later that I would have to negotiate these work-arounds with each new nurse/tech combo, and they were not compelled (probably didn't even have the authority) to negotiate anything regarding my movement, I realized the "work-arounds" were meaningless offerings.  I was on my on to manage the situation as best as I could. 

Really, while my complaints were freely voiced, it seemed the whole thing was a pointless exercise.  While never giving a hint at being persuaded by any of my words, the administrator finally camped out on she herself feeling helpless because of the hospital policy.  How convenient.  She could sympathize with me, but she had no power to change the situation.  And she didn't seem the least bit troubled by it.   In fact, she seemed to see it as her duty to keep to the script.

The message was loud and clear.  No one who actually matters in the relationship of patient/caregiver has any autonomy anymore.  The nurses said they had no autonomy, the administrator said she had no autonomy.  It's as if they all had memorized the script.  It seems I surrendered my autonomy when I presently myself for surgery on Monday night.  Lawyers hold the cards, and in this case a patient suffers for it.  Up to this point, the suffering felt is mostly emotional and mental, but it was suffering, nonetheless.  It was a maddening situation.  A patient, who on one hand was considered well enough to go home, is caught in an algorithm that decides she must be confined to bed or chair with alarms - not because she fell from mobility or other health issues, but because she fell from a stupid choice in footwear.  But there is no blank for explaining things like that.   And there is no way to redeem oneself from this decision.  The decision is made, and it stays made until you leave.  I asked, and that's what I was told.

And for a bit of irony...   When I described what caused the fall to whoever would listen, almost every nurse or technician (and even a different administrator) admitted they have tripped similarly, and recognized how easily the fall happened.  Just looking at the highly polished floors, and the footwear the staff wears, no one had to tell me for me to know that this sort of tripping happens on the job, but I sure appreciated the sense of solidarity it felt like in the moment (even if none of that matter in the case of my "confinement").

And I haven't even mentioned how my health began to suffer between Friday and Monday.  The stress from earlier in the week, waiting day after day expecting to be released, started to look like a cake walk.

To be continued...




Tuesday, September 12, 2023

Part 2: Hospital Stay, Days Three and Four...

I wish I could perfectly piece together the timeline of events of my hospital stay, but days of the same things, over and over eventually just blur some of the details together.  I believe it was on Thursday (the day after I had been told I was fine to go home), I began to develop high blood pressure.  Not off-the-chart high at that point, but significantly higher blood pressure than I'd ever experienced before. 

At this point, I was also still being visited daily by various doctors from the oncology department and infectious diseases.  Sometimes the doctors would change, sometimes it would be a PA.  Technicians were in and out of my room numerous times a day to draw blood.  I remember being told repeatedly that the staph infection wasn't due to anything I had done.  On one hand, I was relieved to hear that, but on the other hand I very much wished it was something I could control, because I would do whatever I could to make sure I didn't end up in the hospital with another infection.  Without coming right out and saying it, I believe they were basically telling me staph was very likely present when the port and catheter was installed.  I had my suspicions from medical articles I'd read online by this point.  My oncology surgeon told me I was the first patient she'd ever had that developed a port infection.  The other oncologists and support staff told me it definitely happens. I appreciated the honesty. I don't doubt I was my surgeon's first infection case, but it didn't help to hear that.  One only has to do a little reading online to understand it's not exactly a rare occurrence.  I wasn't interested in casting blame.  I just never wanted to experience this scenario again if I could help it.

I'd like to note that on Thursday the hospitalist stopped in again, and I took the opportunity to let him know how disappointing it had been that he had spoken to me so confidently of my leaving, and then never got back to me.  To his credit, he apologized. He was kind and humble, and I took some solace in that, but I felt he needed to know the way he handled that situation had been quite a blow to me, and in my estimation there was no good reason for it to have happened.  At the very least, I deserved to hear from him (even if through a nurse) that I would not be able to leave that day.

I remember on Thursday, there was continued talk by doctors who dropped in that the staph infection seemed to have cleared, but they wanted to run more tests to be sure before releasing me. I know one night I developed shivers and shakes again, along with a fever, so it's evidently not as clear cut as one blood test to prove staph is out of one's system.   It also seemed to me that it was on Wednesday that I began to notice that one-by-one, I was being unhooked from different infused fluids and medicines, and injectable antibiotics began to be administered.  I enjoyed the freedom of not having to be unhooked from things just to move around.


On Thursday I noticed the stand still holding bags of fluids and medicines was on the other side of the room.  It was also on Thursday that talk of sending me home with an IV and a plan to have 24-hour unfused antibiotic via medicine balls was agreed to.  It was that or give myself injections of antibiotics every 8 hours.  While I was familiar with the continual infusion of medicine via these balls from after my breast cancer surgery, I also knew I kind of hated them.  But when it came down to it, I hated more the idea of giving myself (or even worse, my husband giving me) injections three times a day.   So the balls won out.  

On my way to getting a mid-line IV put in...


Early on Friday I had a mid-line IV put in (in order to receive the antibiotic from the medicine ball system), and I could see I was finally truly ready to leave.  There was nothing more that needed doing.  I was feeling pretty good for the most part. I was just waiting...

While weary of the whole affair, I maintained a good attitude for a long while, 
trying to find ways to humor myself...


The problem, I was told on Thursday, was finding a home health care company which they could coordinate my discharge from the hospital with a visit from a nurse to set me up with the infusion therapy balls.  I'm not even sure I should be writing this here, but I was told that while, medically, there was no reason to keep me in the hospital, they couldn't release me until they had the home health care situation set up.  It sounded crazy to me.  But I hung onto hope that that solution was just hours away.  

I held onto that thought all day Thursday, and into Friday.   On Friday afternoon I was finally told that a home health care nurse could not come to my home until the following Monday.  That meant that I would be spending the weekend in the hospital.

After days of so much hope and anticipation of leaving, that was a devastating blow.   After a moment of shock, I began to negotiate the terms of my staying in the hospital for essentially three more days (the rest of Friday - through whatever time I left on Monday).   Could I wear my normal clothing?  Yes.   Could I leave the floor I was on?  Yes, with someone accompanying me.  Could I go outside as long as I stayed on the hospital campus?   Yes.   I knew this last one was a stretch, but I had to ask...  Could I actually leave the hospital campus, if I wasn't gone for very long?   Uh... no.  I couldn't be considered as inpatient and leave the hospital on my own at the same time.  That made sense - even if the situation as a whole made none to me.  I decided to be glad for the freedom to wear normal clothing and made some plans to have visitors the next day.

I will also note that my blood pressure continued to be an issue, and as the week progressed my body began hanging onto fluids.  A situation I've never before encountered, but I intuited that since I felt well otherwise, the best thing was for me to move as much as possible, and I was thankful I could at least take walks.  I did everything I could to busy myself - cleaning/straightening my room, making the bed, cleaning the bathroom...  Any little thing I could do to move from Thursday through Friday, I did.  

While spending all this time in the hospital (after being told I was well enough to go home) was not exactly pleasant, I did try to make the best of the situation.  All the staff were very kind, and most encounters were fairly cheerful - even when different people would come to take blood draws, or take x-rays.  Evidently, with fluid filling my body, they wanted to make sure my lungs were clear and organs were functioning normally.  Nevermind that being home and going about my normal life would have surely prevented all of this extra fluid and high blood pressure.  No one seemed to know quite why it was happening.  As if the stress of the situation wasn't reason enough?

Now might be a good time to mention that Greg had come down with a terrible cold early in the week, and except for possibly returning on Tuesday, he had not been at the hospital all week - both because he felt very sick, and with my low immunity I certainly didn't need to be exposed to his germs.  In spite of the stress of staying in a hospital while being told I was well enough go to home...  In spite of a miserably uncomfortable bed to sleep in...  In spite of everything, up to this point I actually considered these extra few days away from his cold were perhaps not completely a bad thing.  Really, most of the time that I was stuck at the hospital I kept a pretty decent attitude.  Admirable, in fact.  

All that said, even with the constant in and out of doctors, nurses and technicians, in spite of the kindness of everyone, and even being thankful for a room with a great view where I could watch all the comings and goings of pretty much anyone entering or leaving the hospital.  In spite of it all, it was a very lonely week and I looked forward to seeing Greg on Saturday morning when he brought me some clothes to get me through three more days.



The large RV above ended up scraping the lamp post the man in red was trying to warn the driver away from.


After some help from a few people, the RV got straightened out again.


And soon headed out of the parking lot:



only to return a few minutes later! 


~~~~~

Yep.  Lots of activity and coming and going happened while I was just waiting...


Grounds keepers of various sorts



School buses dropped off and picked up school children - presumably for appointments?  Treatments of some sort?  

That was a sobering sight.

And all day long people in red shirts valeted people's cars back and forth.  They all looked like retirees, and based on the energy they seemed to have, I concluded they must enjoy the job:




And when I was really lucky I got treated to some beautiful sunsets:



To be continued...


Monday, September 11, 2023

Part 1: Life doesn't always go according to plan...



It's hard to believe I started this post nearly a month ago.  I thought I was getting back into the blogging saddle, but little did I know what was right around the corner.  

It all started on Sunday, August 13th.  It was a beautiful day with our whole family together.  One of the important items on the agenda was to buzz my hair.  I had been missing having all our grown kids together, and they responded admirably to my request to get together.  And middle son's girlfriend agreed to cut my hair off. 

I was told (and read online) to expect hair to begin shedding approximately 2 weeks after my first chemo treatment.  I saw losing my hair as something of a rite of passage during chemo, and didn't view it as all that traumatic of an experience. That said, I appreciate that it is for many people.  We're all different.  Being practical on so many levels, I knew I wanted to be proactive with a plan to buzz it before the shedding began to make a mess.  I couldn't have timed things more perfectly, as the morning of the scheduled hair cut, my between-chin-and-shoulder-length hair starting shedding like crazy.   I was so glad for that.  While I didn't want to deal with the mess of my hair shedding randomly, or experience the emotional toll of my hair thinning, I did want to experience on some level the shedding.  I didn't think it would feel exactly real if I cut if all off before it actually started to come out on its own.   I'm not sure if excited is the right word, but I was pretty pleased that the plan to buzz and the serious shedding happened on the same day.  I felt really lucky somehow.  

If that sounds weird, all I can say is...  in an experience that has a lot of scary and bad stuff in it, I try to take hold of the good where I can find it; watching my hair fill up the garbage container, and not the shower drain, felt like a win.  

It was a good day in all respects.  While I didn't feel all that emotional, I will admit to feeling a tad nervous before the cutting commenced.  But commence it finally did, everyone taking a turn with the hair clippers, my kids trying to encourage me that I could rock the no hair look, wearing caps and scarves.  Young and/or thin women may look cute, even beautiful, sporting their brave bald heads, but I am neither and I was pretty sure I'd feel less self conscious with a wig when out in public.  That said, I sure did appreciate my kids' confidence in me.  But that evening after everyone had gone, looking at myself from all angles in a mirror, I made a mental note to go get the wig I had picked out a week or so earlier.  The day I picked it out (out of a number I tried on), I couldn't quite make the commitment.  That Sunday evening, I decided there was no need to wait any longer to bring it home.  For what it's worth, I discovered I have a huge "Stork Bite" birthmark on the nape of my head.  Imagine, if you never shave your hair off, you may just never know what is lurking under there...

As Sunday came to a close, I began to have a bit of pain at the surgery site on my neck where an infusion port and catheter had been surgically installed about three weeks prior.  While my neck hurt, I didn't get too worried until Monday when I could see a clear sign of infection.  At that point, I didn't waste any time calling the surgeon, and I was given an appointment at the end of the day.  Relieved to be gotten in, hubs and I made the thirty-minute drive to the surgeon's office to get it checked out.  The surgeon immediately diagnosed an infection, but in hopes to save the port, a plan was made for me to start an oral antibiotic that night, and the next day come back to the hospital for an antibiotic infusion.  Feeling really glad I had gotten myself to the doctor quickly, I was relieved this was the plan.  We were so relieved and feeling good about the situation, we stopped on the way home to grab supper.

It was probably an hour and a half later, after getting back home and dropping me off, Greg made a run to the pharmacy to pick up the antibiotic.  Just minutes after he left, I began to feel chilled, and before he could return I began  experiencing uncontrollable shivers and shakes.  Never in my life have I had such wicked shivering and shaking.  I didn't know a body could do that.  Even a low-grade fever is dangerous for someone on chemo, so I kept taking my temperature. At first there was nothing notable, but within a few minutes, the thermometer read 100.4.  Normally, that's not all that exciting of a fever, but after starting chemo I had been instructed to call with a temperature of anything over 100.  My instructions were 100.1 to be precise.   Being home alone, not sure how long Greg would be gone, I started to get worried at how fast a serious fever might grow.  And how long I could tolerate the insane shivering and shaking before I had a muscle spasm.  

I took Tylenol and called my oncologist, and I think he had my surgeon call me.  It was decided that we needed to go straight to the hospital, which is on the same campus as the cancer center - where I had been just a few hours earlier.  The surgeon told me she would meet me in the ER, and she would remove the infusion port that night.  A half hour later we were at the hospital and I was checking in at the ER desk, and within another hour, I was being wheeled into surgery.  The speed at which it all happened was amazing.  I don't know what it's like where you live, but around here, visits to the ER have become legendary for how long one waits to be seen.  And even after you've been seen, sometimes you're lucky to get a room.  It is not uncommon (I've witnessed twice now) to see patients in beds in the hallways.

I suppose because of my doctor's orders, I was on the short list and I was grateful they got me checked in pronto.  Port and catheter were removed, and sometime before midnight on August 14th I was recovering in a beautiful room on the cancer floor of the hospital.  It took until the next day (Tuesday) to confirm I had a staph infection - it was all along the catheter and port.  And then by Wednesday I was told it looked like the infused antibiotics had cleared it up in my system already.  While I was weak, and very tired from the surgery and medicines, no doubt, I thought I was the luckiest gal alive to have a scary infection clear so quickly.



Early Wednesday afternoon, a hospitalist visited my room and told me I could expect to go home later that day.  My middle son happened to be visiting me at the time, and I was glad I had a witness to (and another participant in) the conversation.  Son (who just happened to be in the area that day) made plans to hang around and take me home when I was discharged - we were told it could take a couple of hours for all that to happen.  The hospitalist said he'd run the decision by the infectious disease doctor and oncologist, but he spoke so confidently about me leaving, I and son began making plans to get me out of there.  Son ran some errands, I got myself at least mentally ready to leave - nearly giddy with relief at the thought of going home.

Two hours passed, and when a nurse came into my room again, I eagerly asked her when I'd be leaving and she told me flatly, "You're not leaving today."   I told her a doctor had told me earlier that I could expect to leave in a couple of hours.  Doubtful, she checked the computer.  There was nothing there to indicate anything of the sort.

Confused that I would be left hanging like that, with clearly no intention of that doctor communicating anything different than he had told me earlier, I was stunned and understandably disappointed.   Not seeing any other choice but to accept it, I settled in for another night in the hospital, thinking and hoping I'd be leaving the next day.

This began possibly the most surreal experience of my life. 

To be continued...


Thank you Peggy B. for this sweet bouquet of fun and pretty flowers.