Team Diabetes Canada logo
Home Our Stories Why Diabetes Fundraising Sponsor Us Events Email Us


Friday September 8th, 2006 - We get the call to start dialysis on Monday.

 

 

Monday September 11, 2006

 

DAY 1

 

 

Upon leaving the elevators we see exactly where we need to go...

 

 

We are all nervous smiles while checking in.

 

 

This is all the medications Johnson takes so far on a daily basis, now we need to add dialysis to this list!

 

 

This is the exactly the type of catheter that was inserted into Johnson's abdomen 8 years ago.

 

 

This is what a file 8 years old looks like.  Johnson's file is approximately 3 inches thick!

 

 

The doctor's prep Johnson for surgery.  I'm not feeling so good!

 

 

Here Johnson is nervously waiting to be frozen and cut open to remove his catheter.

 

 

The doctor's make the first cut.  Johnson is not prepared for the all the digging and tugging that will take place for the next 60 minutes or so.  I am feeling very faint, and must sit down several times to catch my breath.  Johnson thinks I'm fine cause he can't see me.  I try to keep my voice very positive, and crack a few jokes, but I really want to be sick!

 

 

The catheter is finally removed safely without it being damaged.  I'm definitely going to need a stiff drink tonight and the day is just getting started!

 

 

A close up of Johnson's catheter...ewe!

 

 

Our nurse takes care with Johnson and dresses his wounds.  This nurse is so nice to us, and will be with us for the next several weeks teaching us everything we need to know.  She helps to put us at ease.

 

 

September 11, 2006...
Dialysis starts for Johnson.  Another reason September 11th will be forever remembered in our household.

 

 

Johnson putting on his brave face...we take a breath...we think the worst is over.

 

 

I take this picture of myself!  Yes I know it is not very flattering and in reality I'm much better looking!  But if Johnson is willing for us to all look at him...I think you all deserve to see me at my best!  Ha ha!  As you can see...I am rather pale and gross looking.  This is me saying YUCK!

 

 

I show Johnson the picture I just took of myself!  He is in pain and tells me to stop making him laugh cause it hurts!

 

 

Our nurse hooks up our first bag of fluids...it weighs 5lbs.  This fluid will be inserted every 4 hours into Johnson's abdomen where it will sit 4 hours and then be drained.  This is called an exchange.  So if you think Johnson is looking a little bloated, think about an extra 5lbs of fluid you have to carry around all the time!  Johnson will have to do 4 exchanges a day.  Each exchange take approximately 40 minutes.

 

 

The exchanges are NOT successful.  No fluid goes in and none comes out.  It is suspected there is some type of blockage in the catheter.  Heparin is injected into his catheter to dissolve any fibrous material which could be clogging the catheter. 

 

 

Here we are leaving day one.  We must now wait overnight and try again.

 

That night is hard on Johnson and I.  The reality of dialysis hits us HARD!  We have a good cry...OK I have a good cry...he does not like what has happened to him.  He does not want to have to do dialysis for years while he waits for a kidney.  I have started the testing to see if I can give him one of my kidneys.  Our blood type matches...my tests continue this week, and if I am accepted, we hope to do the kidney transplant by January 2007.  Wish me luck!

 

DAY 2

 

 

Our nurse collects fluids from Johnson dialysis bag, as our first attempt at dialysis today is not successful.  There is still blockage.  Our nurse tries the push/pull technique with the needle injected directly into Johnson's catheter to see if she can pull out any dissolved fibrous material which could be blocking his catheter.

 

 

Many attempts at dialysis again today, none successful.  More Heparin is injected and we will try again tomorrow.  Looks like the catheter is either really blocked, or may have moved into uncharted territory.  We are scheduled to go for a special x-ray on Thursday where they will inject a small wire into his catheter to see if they can remove any blockage.  If during the x-ray they see that the catheter has moved, then another surgery may be necessary for Johnson to put it back into proper place.  This x-ray procedure can be uncomfortable for Johnson...we have come to learn that uncomfortable really means PAINFUL!

DAY 3

 

We are to meet with Johnson's diabetic doctor.  So far you have just heard about our Nephrologists (Kidney doctors).  Today we talk more diabetes.  You see...Johnson has two very critical illnesses.  Type 1 Diabetes, and Renal Failure (Kidney Failure).  Each is dealt with individually and then collectively.  I will update you all again when I can.

We met with Johnson's new diabetic doctor. He was a very stern Doctor, who definitely intimidated us and didn't have much of a bedside manner!  After he found out Johnson was from Pakistan he loosened up and even cracked a smile at one of our jokes. 

Johnson is to take a few more units of insulin each time now to try and bring his blood sugars a little lower during dialysis, as the dialysis fluid is full of glucose.  We ran into a fellow Innovapost colleague at the diabetic centre, who has been diabetic for over 21 years and it was nice to see a familiar face. 

Johnson learns to add Heparin to his CAPD bags. (Continuous Ambulatory Peritoneal Dialysis) or PD for short.  He must be extremely sterile when doing this to ensure he does not contaminate anything, or else he must throw everything away on this table and start again.

 

Johnson practices his proper handwashing techniques.  He thinks his hands are very clean.  Then our nurse has Johnson rub a lotion on his hands which glows in the dark under a blue light to show us where there is still bacteria.  Let's just say...his hands were VERY blue!  ewe!

 

 

Johnson learns to draw out Heparin without contaminating anything first time round!  Guess it's been those 24 years of drawing out insulin which makes this easy for him.

 

 

Johnson must inject the Heparin into his practice bag without contamination.  He does great!

 

 

Tomorrow we will meet the radiologist who will try to unblock his PD catheter.

 

DAY 4

 

Today we attempt to unblock Johnson's PD catheter at the General Hospital.

 

 

Johnson checks in to radiology.  I am holding my breath and am nervous.  This procedure is known to be uncomfortable. 

 

This day is a bust.  The radiologist meets with us to discuss the procedure.  He finds out Johnson's catheter has been in for 8 years unused, and tells us there is a 0 to 1% chance this procedure will actually unclog his catheter.  He refuses to try and sends us back to the Riverside Hospital to be reassessed by his doctors.  The Radiologist suggests that we have the surgery to remove this old catheter and add a new one. 

 

The doctor on rotation in the dialysis unit today agrees with the Radiologist, and then it is decided that tomorrow we will try injecting dye into his catheter to see if there is any flow.  We feel this is going to be a waste of time.  Most likely we will need the surgery.  The problem with this is that we will need to schedule this operation, then once the operation is performed, Johnson will need at least 4 weeks to heal before the catheter can be used for dialysis.  What could happen?  Johnson's health could deteriorate over this time period and he could get very ill.  If that were to happen, then Johnson will have to have Emergency Hemodialysis performed through a vein in his neck.  Yuck!  So far this week has been a week of Stop and Go for us, which has been emotionally exhausting.  We catch naps whenever we can!  Depending on what we are told tomorrow, you may all see us back at work on Monday if we have to do the waiting game.  Please send prayers our way!  I will update you all when I can.

 

Continued...