Todd's Journey

The story of my cancer journey

Todd's Journey - Chapter 16

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Here is Chapter 16 of my cancer Jouney.

Neph tubes gone!

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Procedure went well this morning. The nephrostomy tubes were removed, and stents were inserted. They seem to be working fine so far, and I seem to be slowly getting back to normal urination.

I do have a bit of pain right now but that is irritation caused by the catheter that was temporarily in place.

The pain should get better over the next few days.

Update on go forward plan

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Hi Everyone,

Happy New Year!!

Tomorrow I will be going in for a cystoscopy followed by a potential stent insertion. The whole experience should take about an hour, and I will be out for the procedure.

Since completing my chemotherapy, my urological oncologist has not been able to adequately look at the inside of my bladder. Tomorrow he will do so and determine how well my ureters are draining from my kidney to the bladder. If they look relatively good, he may be able to remove the neph tube, and allow the kidney to drain into the bladder on it's own, or he may insert a stent from the kidney to the bladder along my ureter to assist in the draining, and then remove the neph tube.

The default option for tomorrow will be to insert stents into both my kidneys to the bladder, and to remove the neph tubes.

The stents might then come out in a few months if I can't tolerate them, or the draining continues to improve.

I will post a message to you all on Wednesday to let you know how it all went.

Hello All,

As you probably know, I am to undergo another procedure on January 2nd to determine if my neph tubes can be removed.

Speaking with Dr. Morash today (my urological oncologist) the plan is to enter the bladder to take a good look of the lay of the land. Previously the cancer tumors in my bladder were blocking (or partially blocking) the ureters which did not allow the urine from my kidney to drain into my bladder.

The three previous resections of my bladder attempted to remove as much of the tumor as possible, but they were not able to get at any tumor that was in my ureter. In fact, during those surgeries they were not able to even see the entrance of the ureter from within my bladder.

The hope now is that the chemotherapy, which was highly successful at reducing the tumor and node sizes in my lungs and elsewhere, will have reduced the size of any potential tumor that was in, or around, the ureter entry into the bladder.

The plan is to see if they can identify (see) the entrances to my left and right ureter, and assess if the flow of urine from my kidney is entering my bladder. They can do this using dye to watch the flow.

If the flow appears good, they may put in some stents (temporarily) to ensure the flow remains ok, which would allow me to remove the nephrostomy tubes.

It is also possible that the flow would not be great, in which case the stent would help, but if not enough, the neph tube would have to remain in place.

The goal of the procedure on Tuesday is to try and remove the neph tubes (or at least one of them) to allow me a bit more freedom and convenience in terms of quality of life. They may be able to do this with stents, or if the flow is very good, they may not have to place stents at all.

We won't know what the outcome of my neph tubes are until after the procedure on Tuesday. If I am lucky, I will wake up from surgery with no tubes, or at least one less tube. I will update everyone on Wednesday or Thursday next week.

Wish me luck!!!

Update on Nephrostomy Tubes

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Hi Everyone.

I am scheduled for a cystoscopy on January 2nd under anesthesia in order for my urological oncologist, Dr. Morash to take a good look at the inside of my bladder.

He is going to assess whether or not I need to keep the nephrostomy tubes, or if ureteral stents could be put in from below to help the flow of fluid from my kidneys to my bladder.

It is possible that the chemo shrunk the tumors that were originally blocking the flow into my bladder that I will no longer need the nephrostomy tubes or a stent.

All will be figured out on January 2nd. Either I will come home with no neph tubes, or will have to keep wearing them for a while.

Keep your fingers crossed.

Tubes may be coming out now

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Hi Everyone,

My urological oncologist, Dr. Morash, is booking me in for a day proocedure on January 2nd, where he is going to look at the inside of my bladder and possibly place stents in my ureters in order to get rid of the nephrostomy tubes and bags.

This would be so nice for me, as the neph tubes are truly very restrictive and inconvenient. Having the tubes removed will allow me to return to much more normal activity and give me great mobility in my daily life.

So, all in all it looks I may be started off the new year NEPH TUBE FREE!!!! :o)

Still have the tubes!

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Well, I was hoping that maybe when they changed my nephrostomy tubes yesterday, they might actually remove one, but that was not to be. I guess my urological oncologist, Dr. Morash, decided to wait a bit longer to remove them. Perhaps after I finish my neo-adjuvant chemotherapy on November 30th, they may look to removing them then. It would be a nice Christmas gift to have them gone.

Other than that, I am definitely a bit more nauseous this time. Was sick twice yesterday after eating. It could be related to the new neutraphil booster shots I am taking. Tomorrow is the last day for the shots so we'll see if my nausea improves.

Also have much more fatigue this round. Been sleeping a lot more than previous chemo sessions. They did say that some of the side effects of chemo build up each cycle, so this could be a normal result of the 3rd cycle.

Anyhow, going for bloodwork today to see if I am able to take my chemo on Thursday. Will keep you all posted.