Yesterday was the follow-up to my June 09 prostate surgery. The Civic is a city hospital without a ton of parking. Shauna takes time off work to get us there so that I don't have to navigate the traffic and then search for elusive parking. We go by expressway, but it does get quite busy the farther we drive into Ottawa. With the dearth of parking, she drops us and heads to the mall.
This was to be a flow test. I was instructed to come with a full bladder and to bring water with me. Timing a full bladder isn't easy, so I began consuming water in the car. I left it that long because I didn't want to drink too early and arrive in dire straits. As it turned out, they took me right in, but I only had a small dribble. Back in the waiting room, I drank the container that I had brought with me and filled it twice more. About a half hour later, I was ready to try again, and a nurse came to escort me to urinate into the cone-shaped device that metered my output.
I certainly flowed this time: more copiously than usual and at what seemed to me to be at a greater rate.
I was then taken to a nearby, small and very cool, as in cold, room where they administered an ultrasound to determine how much water I had retained after urinating. The nurse seemed to think that was quite a bit, but the doctor later opined that was quite good.
Exit nurse. Enter doctor: not my surgeon but an urologist in training. She asked questions and noted my answers, all with her back turned while banging away on the computer. She asked the usual, such as how many times I got up at night. I replied, perhaps cheekily, that it depends on how long I slept. Lest she think me too impertinent, I hastily added that it was roughly every two hours on average, sometimes only an hour and sometimes three. I told her about my UTI and 'fainting' spell. possibly brought about by straining,. She didn't comment but kept typing.
Out she went and returned minutes later with the surgeon, who said that my flow rate was not great. I replied that it had seemed to me to be one of my more impressive flows. There wasn't much more jabber before he said that he needed to get in there to see what was going on. "No, not today, we'll let you know." Sigh, I will have to do this somewhat major excursion again.
If you haven't picked up on my situation, it is this. After my 4th prostate surgery in June, I had high hopes, but by only 6 weeks, I had regressed to something resembling my previous, sad state.
Things got better at the restaurant for an early supper. Shauna ordered a a barbequed chicken salad sandwich with sweet potato fries. Sue and I opted for a twofer: one appetizer, one desert, and two entrees for one price. Being charitable people, we shared the appetizer with Shauna. I assure you that all was very yummy.
I understand the part about time with the two ladies. The prostate part must be frustrating!
ReplyDeleteHope this time it is cleared up properly. Fingers crossed for a good outcome.
ReplyDeleteIs a Stent possible? I am sorry that once again you are again dealing with the same old....well...we can't call it crap, can we? I would never have thought of pairing caramel with cheesecake. But dinner sounds yummo!
ReplyDeleteSo sorry this is still going on and needing yet more treatment, that's really stressful. Any test needing a full bladder and timing is stressful in itself. Btdt!
ReplyDeleteI'm glad some parts of the day were good though. You have a nice daughter there.
Such a lovely dinner, and I liked the photo with the man full length, so I could see his Berks with socks. I had a scare in the middle of the night of terrible dizziness, but it seems to be gone now. Believe me I was holding onto furniture! I sure hope the doc and procedures can help your condition. Not much fun when all they seem to care about is writing the notes.
ReplyDeleteWhile I thankfully don't have prostate issues... yet, I wouldn't have enjoyed your meal with lactose present in all three courses.
ReplyDeleteMy husband elected not to do surgery for the same issues. At this point it is becoming very difficult for him to 'go' and takes a very long time. However to combat edema he has to take a 'water' pill which makes things so much harder. Especially since he isn't able to empty out fully any more. Hospice has recommended a Foley and it seems that this may help his sleep at night as he has the same sort of problem you are having.
ReplyDeleteI really hope the doctors can help. I can only imagine. LOL, I never imagined I'd be discussing this with anyone!
I love the photos and the gent with his Berks on. A dinner was well deserved.
I am glad 😊 the food was good. Let's hope 🙏 for a good outcome.
ReplyDeleteAt least the day ended well.
ReplyDeleteGood food can make everything a lot better. I'm sorry you have to go through this all over again.
ReplyDeleteI'm glad you had your ladies, the comfort from food and their company offset the gray of the morning. I do hope you get some actual real relief soon.
ReplyDeleteI'm sorry you have to undergo the procedure again. If it means extra time with family, that's a bonus.
ReplyDeleteThe Francophone, as you call him, is wearing socks with sandals!! That's a definite no-no here. 🤣😂
Sigh...what a trial for you. Dinner did look good and time spent with daughter is precious.
ReplyDeleteMy dear friend, I'm sad that you have to go through this again. I will keep healing energy flowing your way. It is good you were able to spend time with your daughter. Breath, think positive thoughts and all will be well.
ReplyDeleteI have to wonder why the chicken fried chicken redundancy and so I will be looking that up.
ReplyDeleteYou're so right about the French flare for fashion. I don't know what it is, but surely the simple addition of a scarf can't be all there is to it! What is their secret!
So sorry about your flow problem. And those pesky UTIs can make a grown-up cry!
ReplyDeleteThe photo is nice though...and the food is a definite winner.
Here's to better week!
hugs
Donna