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Author Topic: Bob's Blog 4-4-13: Technology Marches On (and Over) Dialysis Patients  (Read 2135 times)
BobN
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« on: April 04, 2013, 05:20:47 AM »

Bob Here

I was reading about the wondrous advances in technology exhibited recently at the Consumer Electronics Show.  Self-driving cars, 3D printers, smart phones that do everything short of walking the dog.

Pretty amazing stuff.

It gave me something of a sense of elation that we live in a day and age when such innovation and cutting-edge thinking is possible.

Then, I tried to program my VCR and got so frustrated with the process, I wanted to rip the whole assemblage out of the wall and toss it out the window.  I went to run some errands and couldn't get my garage door opener to work. I got in my car, and couldn't figure out how to adjust the clock for the time change.  The ATM at my bank was on the fritz.  It said to push a button for help, but when I pushed it, nothing happened.

I thought, well, so much for our technologically advanced society.

Now, I should point out that, in general, technology and I do not make a good mix.  I'm one of those people who can cause something to malfunction just by going near it.

Before I retired, I was on a first name basis with the tech support people in my office.  They practically wanted to establish a frequent-caller program based on me alone.

A lot of times, the fix that I needed would be something really simple and I would be embarrassed by taking up their time.

Here's an example of one of my interactions with Tech Support over the phone:

TS:  "Tech Support, may I help you?"

Me:  "Yes, I moved my office around yesterday and now my computer monitor won't work."

TS:  "Okay sir.  By any chance, did you plug it back in?"

Me:  [Pause]..."Thank you very much.  Have a nice day."

It got so bad that I heard a rumor they were planning on opening a satellite office on the floor of my building.  I'm pretty sure everyone would have known that I was the cause, but I was spared that embarrassment when the change never came about.

So, knowing what you know now, what would you say would be the absolute worst change a dialysis patient like myself could make to his treatment regimen?

How about moving from in-center treatments, where anything having to do with the machine is taken care of by technically astute and trained individuals, to doing treatments on my own at home, where the chances for catastrophe increase exponentially?

You got it.

As you know from last month's blog, I'm now doing home hemo, with my faithful and loving wife trying to avoid getting sucked into the vortex of equipment misfortune that seems to follow me around.

In order to do home hemo, you have to go through an intensive four-week training program.

It's a wonder the training facility survived my sessions.

We were on our first lesson, walking back to the room where they kept the home hemo machines.  That's where we would both train and have my treatments.  The nurse/trainer was telling us about the advancements of the new machines and how far fewer alarms were going off.

No lie, as soon as I walked in the room, the alarms on two of the machines started dinging.

There were no patients on them, in fact, the room was empty.

"Hmm.  That's strange," said the nurse, walking over to reset the machines.

My wife was eying me suspiciously, but I just smiled weakly and shrugged my shoulders.

She was probably thinking, "Oh boy.  This is gonna be a long haul."

Now, before we started training, I was told to arrive "dressed comfortably, in your typical dialysis clothes."

Turns out, I would have been better off wearing a bathing suit.

The initial instructions were somewhat helter skelter.  It was apparent that we were going to learn about the process on the fly.

O maybe on the swim.

Our initial lesson involved pre-mixed dialysate bags, as opposed to using the pureflow machine underneath the cycler.  Those of you doing home hemo know that the pureflow makes the dialysate using your water at home.  But when you travel, or for whatever reason can't use the pureflow, you use these pre-mixed bags.  The bags are modestly heavy and my machine was up against a wall, so I practically threw my back out hanging up the ones in the back.

My instructor had an amused look on her face.

"You might try spinning the rack around," she said.

"Oh yeah.  That would probably be easier," I said, but I felt about an inch tall.

Anyway, during the setup process, I got confused over what to clamp when, and suddenly, dialysate was pouring out all over the floor.

Oh, and the machine alarm started going off.

My wife just backed away, hoping that whatever my problem was it wasn't contagious.

I was in a total panic, saying something brilliant like, "Oh crap.  What do I do know??"

My instructor calmly said, "Close the clamp."

I said, "Right.  The clamp.  Got it.  Which one??"

"The one right above the fluid pouring out."

"Oh yeah, hah hah."

So, I got the clamp closed and Niagra Falls stopped flowing.

It took us a few minutes to mop up the mess, then suddenly we hear a shrill "BEEP BEEP BEEP BEEP..."

I nearly jumped out of my drawers.  This was much louder than the machine alarms we heard earlier.

Of course being the calm type, I yelled, "WHAT IS THAT??"

"It's the fluid detector," said the instructor, still calm.

Meanwhile the infernal thing was still going off.

"Well, we know it works...how do I turn it off??" I asked, thinking that my first impulse to throw it against the wall probably wasn't correct.

"Take it out and dry it off with a paper towel," said the instructor.  So, the wife took car of that.

The instructor still had a half smile.  "You can just skip the step in the process where you test the battery of the detector," she said.  Now I could tell she was making an effort not to laugh in my face.

Anyway, we cleaned up the flood and continued with the setup process.

Everything was going along okay, then we learned about snapping and tapping the lines.

Some of you probably know that this is how you remove excess air from the dialysis lines so you don't get an air-detector alarm during your treatment.

Heaven knows, I had already heard enough alarms for my liking.

The wife and I decided that we would take turns doing this so we could both get some practice.  She snapped and tapped the arterial line and everything went just fine.

I was doing the veinous line, thinking that my earlier disaster was just an anomaly.  Snap, tap, get the air bubbles out.  I got this.  Heh heh.  I'll be an ace at this process in no time.

I was tapping up near the top of the line, when the connection to the saline bag came undone and fluid started pouring out all over the place.  Of course, the fluid detector started going off again, and before we knew it, we had another flood on our hands.

"Close the clamp," said the instructor

"Right.  Of course," I said.  Then I closed the clamp on the line instead of the one leading to the bag and the waterfall continued.

"No.  The other one," she said.  Now, she looked like she was going to herniate herself, keeping from laughing.

When I finally closed the right clamp, I was drenched.  The fluid detector and machine alarms were both going off, and there was saline all over the floor.

The instructor and the wife were both just looking at me trying not to laugh.

"So," I said calmly.  "How do you think it's going so far?"

Then the three of us were cracking up.  It took us about ten minutes to stop laughing.

But, like any other process, home hemo gets easier as you do more treatments.

We've learned some of the nuances of the process, since our instructor decided to live dangerously and allow us to do my treatments at home by ourselves.  We've learned about real in-depth technical terms, like 'Mr. Peanut' and the 'chickenfoot.'

The home machine is really a technical marvel, and, so far at least, I've survived despite the fact that we're not.

Thanks for reading.  I hope everybody thrives in his or her dealings with modern technology

Take care.

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www.bobnortham.com
Author of The ABC's of the Big D: My Life on Dialysis
Bob's Prescription for Living With Dialysis:
Follow Your Recommended Diet and Especially Watch Your Potassium, Phosphorous, and Fluid.
Stay Active - Find a Form of Exercise You Like and DO IT!!
Laugh Every Chance You Get.
amanda100wilson
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« Reply #1 on: April 04, 2013, 06:12:07 AM »

Bob, you are not alone.  hat is part of the course.  It all becomes second nature pretty quickly.  you will still foget things from time to time but will become comfortable with dealing with them.  I am glad to hear that you are switching.  it will be a wonderful feeling of liberation, but don't worry if a few months in, you get burn-out.  just stick with it.  oh, and try to leatn to do as much for yourself as possible.
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ESRD 22 years
  -PD for 18 months
  -Transplant 10 years
  -PD for 8 years
  -NxStage since October 2011
Healthy people may look upon me as weak because of my illness, but my illness has given me strength that they can't begin to imagine.

Always look on the bright side of life...
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« Reply #2 on: April 04, 2013, 08:45:35 AM »

Bob, please go ahead and pull the VCR from your wall and throw it out the window.  There is Blu-ray.... go to Best Buy and ask for it.

            :rofl;
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« Reply #3 on: April 04, 2013, 11:56:39 AM »

A similar thing happened to my mom when I started dialysis back in the 1990s.

The children's hospital that I went to had a unit called the Care By Parent unit, which was exactly as it's name implies.  They put kids here who were going through some kind of treatment in hospital that the parents would have to continue when they got home.  This was kind of like a half way house for parents.  There is one nurse on duty during the day, but at night, you're pretty much on your own.

Back then, the PD cyclers were not the compact, suitcase-sized machines that they are today.  They looked like the granddaddy of IV pumps (though they were not a pump at all, they ran on gravity) and had bags hanging at different heights for different purposes.  The sets were designed for a 4 day use, though the warranty only covered 3 days (figure that one out. *L*), and this was also back when you still had to spike bags.  The sets had 12 lines for dineal bags, so because of the size of the bags we were using (3 litre) and my small fill volume (1200ml) I only needed to use 3 lines per night.  When you set up for the first night, you needed to clamp all 12 lines, or you'd get a leak, which meant contamination, and you had to start over.

So, Mom and I were transferred to the Care By Parent unit after she'd finished her training, and I sat down to watch Mom set up my machine for the first time.  All seemed to be going well until I heard dripping, and a few choice words come out of my mother's mouth.  She had forgotten to clamp one of the 12 lines.  Luckily, the kidney ward in the hospital was only a floor below, so Mom called them and explained what was going on.  She then sent me downstairs to get more supplies while she stripped the machine.

Ten minutes later, new supplies in hand, Mom started over, only to hear that dripping sound again.  After a few more curse words and another call downstairs, I found myself standing at the nurse's station in the kidney ward for the second time that night.  The nurse just gave me a silly grin as she gave me half the supplies to carry before starting back up the stairs again.

Third time was a charm, that night anyway.  In the year and a half after that, until I got my first kidney, I can happily say that she never ever missed a clamp again.
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Dialysis - Feb 1991-Oct 1992
transplant - Oct 1, 1992- Apr 2001
dialysis - April 2001-May 2001
transplant - May 22, 2001- May 2004
dialysis - May 2004-present
PD - May 2004-Dec 2008
HD - Dec 2008-present
BobN
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« Reply #4 on: April 05, 2013, 02:07:52 AM »

Amanda, I'll definitely stick with it.  The pros are outweighing the cons so far.

Rerun, I'm equally inept operating my Blue Ray player, but I keep trying!

Riki, great story.  I have to admit to a few choice words of my own when those leaks happened.
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www.bobnortham.com
Author of The ABC's of the Big D: My Life on Dialysis
Bob's Prescription for Living With Dialysis:
Follow Your Recommended Diet and Especially Watch Your Potassium, Phosphorous, and Fluid.
Stay Active - Find a Form of Exercise You Like and DO IT!!
Laugh Every Chance You Get.
Angiepkd
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« Reply #5 on: April 05, 2013, 09:01:45 AM »

Your stories crack me up! I think having a great sense of humor makes everything better. I have been doing home hemo on my own for a week and have had some oops moments myself, but it's all worth it.  I feel better than I have in years!  Plus, I can dialyze in my jammies without freezing lol!  Keep up the good work!
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PKD diagnosis at 17
Cancer May 2011, surgery and no further treatment but placed on 2 year wait for transplant
October 2011 first fistula in left wrist
April 2012 second fistula in upper arm, disconnect of wrist
January 2013, stage 5 ESRD
March 2013 training with NxStage home hemo
April 2013 at home with NxStage
April 2013 fistula revision to reduce flow
May 2013 advised to have double nephrectomy, liver cyst ablation and hernia repair. Awaiting insurance approval to begin transplant testing. Surgery in June.
June 2013 bilateral nephrectomy.
August 2013 finishing testing for transplant, 4 potential donors being tissue typed.
January 2014 husband approved to donate kidney for me
March 4th 2014 received transplant from awesome hubby. Named the new bean FK (fat kidney) lol!  So far we are doing great!
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« Reply #6 on: April 05, 2013, 07:36:14 PM »

I've had a few "oops" moments myself over the years while on PD.  There were a few times where I disconnected myself, forgetting to clamp my catheter clamp.  The carpet in my bedroom at my mother's house has some rather nasty stains because of it.
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Dialysis - Feb 1991-Oct 1992
transplant - Oct 1, 1992- Apr 2001
dialysis - April 2001-May 2001
transplant - May 22, 2001- May 2004
dialysis - May 2004-present
PD - May 2004-Dec 2008
HD - Dec 2008-present
BobN
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« Reply #7 on: April 06, 2013, 03:19:12 AM »

Thanks Angie.

I have had lots of oops moments, but fewer lately, so maybe I'm getting the hang of this.
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www.bobnortham.com
Author of The ABC's of the Big D: My Life on Dialysis
Bob's Prescription for Living With Dialysis:
Follow Your Recommended Diet and Especially Watch Your Potassium, Phosphorous, and Fluid.
Stay Active - Find a Form of Exercise You Like and DO IT!!
Laugh Every Chance You Get.
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