I'm sure there are plenty of you who feel like I do. It's been just over 36 hours since I received my diagnosis of stage 1 bladder cancer. It feels like a weight on my head and shoulders, but a slight improvement to immediately after diagnosis, when I felt for most of the day like the walls were closing in around me.
The doctors and nurses at the hospital (Aintree, Liverpool) said quite a few things, half of those things went right over my head because I was in a daze and not taking anything in properly. I hadn't read my NHS letter until I was in the waiting room because I've moved house very recently and only grabbed it from the old house the previous afternoon. I thought I'd be turning up, peeing in a pot, having a quick blood test, quick scan with a machine and I'd be sent on my way, but cystoscopy? OK, I had one when I was about 11, it'll be fine I thought.
Fast forward to after the (uncomfortable!) procedure, followed by a very rummagey prostate examination, I'm led over to a screen where the doctor started talking about something, but I wasn't taking it in because the cystoscopy/prostate exam combo had made me feel queasy, then I started sweating, went really hot and nearly fainted. Then they asked "Are you feeling sick because of the news?" "What news?" I asked, not having taken anything in. Then I was quickly whisked away to the recovery room with a gaggle of nurses checking my BP and pulse, and bringing me tea. This is a bit full on for feeling faint, I thought. Then the doctor appeared again with a cancer nurse, and it was only then when they started to explain that I really got to grips with what was happening to me.
So yeah, from "It'll be a quick scan etc, it's fine" to "What the ****, I have cancer?" all in less than an hour. To say I was unprepared is an understatement.
What I'm dealing with so far: Apparently its stage 1 bladder cancer. Superficial non-muscle invasive carcinoma. There is also a lump on my prostate, which is "grossly enlarged", and they don't yet know if it's something benign or something worse. I've had trouble passing water for some time now, along with sudden urgency, not being able to empty the bladder completely, etc.
That's how things are for me at the moment. I've had to leave a message with the hospital to get a call back so that I can check what's actually going to happen because I was too overwhelmed and nothing went in. I think the intention is to operate in the next few weeks. I know nothing beyond this at the moment, and obviously it's all really daunting, but could be a lot worse.
Just an intro post really, no questions to ask. Just an account of where I am at the moment. Hoping to get some support from here, as well as offer support to people going through the same thing as I am, when I'm in a position where I'm capable of doing so.
Dear Oscar,
Yes it's a shock even if one is expecting it, so we all understand how you feel. Over the next few days it will begin to sink in but please do not be too despondent. It seems they have caught it early and they will do all they can to get you through this. Well done for going and getting checked out.
There are people here with all levels of seriousness of cancer all managing symptoms and concerns. Many more have passed through on their journey and are back living their normal lives.
I won't bore you with too much jargon but the operation you've been told about is a TURBT - they put you under then go in and take a sample of the cancer to test. Although sometimes everything can be resolved at that stage and it seems from what you say that they are hoping that will be the case for you.
By the way, ir seems that although we all have bladder cancer, different hospitals and surgeons do things slightly differently so don't be concerned if you read here that someone has something done in a different order or way. For example, I wasn't told I had cancer at my cystoscopy - though during it they did show me something that looked like a cross between a verucca and Denis the Menace. I only learnt what it was at the feedback meeting several weeks after the TURBT. (You can see our bios if you click on our name).
You'll notice I haven't mentioned the prostate - I don't have one but I do know people have have had your symptoms of urgency etc and been successfully treated for them in various ways, depending on cause.
It's 3 years since I was where you are now and I've learnt a lot, met some wonderful people, and am out the other side having regular checkups and back to everyday life.
We'll help you get there too.
All rhe best,
Latestart
(Born 12 miles down the A56 from you in St H though haven't lived there for many years.)
Hi, welcome to the forum and hope you find my response below helpful too,
All the best,
Latestart
Thanks! nice to meet you. how the days of life are spending
Hi Oscar4fefce,Welcome to our friendly group though I’m sorry you find yourself here.
It will take time to adjust to your diagnosis,it’s such a shock at first.
The next stage will be a TURBT procedure ( Trans urethral removal of bladder tumour) where as much of the tumour is removed under a general anaesthetic.They will take biopsies and once the histology results are back a MDT ( multi disciplinary team made up of various medical people) will discuss the best course of treatment for you.It’s usual to get some type of scan at diagnosis.It’s best to take things one step at a time at the start otherwise it can feel overwhelming.
This group is very supportive so I hope you will find it helpful.Best wishes Jane
Hi notyourar1dc2bb,Welcome to our friendly group.I hope you will find it helpful and supportive.Best wishes Jane
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