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My Radical Radiotherapy Starts Today!

User
Posted 14 Oct 2014 at 05:51

Hi,

The day has finally arrived.

Royal Berkshire Hospital, 8.30am.  Start of 19 fractions of RT.

Four weeks that could change my life.

Feeling nervous.

Steve

User
Posted 16 Oct 2014 at 16:27

Hang in there Steve, they will sort it out.

Ali x

User
Posted 22 Oct 2014 at 07:10

Ouch! Sorry to hear that Steve.

You probably don't want to hear this but the tablets are not a quick fix, mine sort of edged in over a few days.
I'd ride their back if I were you until you get the tablets in your hand.
Perhaps ring them in the morning to enquire if the Oncologist has given the ok, saves wasting all the day until you turn up late afternoon.

I'm surprised at the perceived relaxed attitude to your condition, when I hit these issues it was all done and dusted in an afternoon. I mentioned it, an infection test was done, I walked out with the tablets. Plus LOTS of warning that if it got worse or stopped completely I had to present at A&E PDQ to be drained before my kidneys exploded (I may be embellishing a bit there)

I'm guessing that as you are having a reduced visit / higher fraction treatment path the teams are unsure of the correct protocol.

Best of luck,

Kevin

User
Posted 22 Oct 2014 at 08:38

Hi Steve

Had the same time frame and daily dose (3DRT) – loads of issues with frequency but no issues with flow whilst having RT. As an side it was nigh on a year before my consultant put me on tablets as he felt it was better to wait for damage to self heal – it didn't nor hasn't.

As Kevin said , tablets are not a quick fix. Don't take risks if you can't pee – get it sorted.

Good luck with RT

Ray

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User
Posted 14 Oct 2014 at 11:34
Good luck Steve, 4 weeks will fly by. Try to keep your bladder filling the same every time. You will find your own ideal time to fill up, mine was drink 4 cups at 40 minutes to go and finish them with 35 minutes to go, enjoy the ride into the scanner and relax its a doddle.

Roy

Edited by member 14 Oct 2014 at 11:52  | Reason: Not specified

User
Posted 14 Oct 2014 at 11:39

Good Luck Steve,

 

I hope you enjoy your daily RT as much as many of us have done, and that you'll reap the benefits later.

It will be over before you know it.http://community.prostatecanceruk.org/editors/tiny_mce/plugins/emoticons/img/smiley-wink.gif

 

Someone said recently that while he celebrated completing all the sessions, he felt a bit 'flat' when the routine ended.

That's very true. I found myself missing the staff and the friends I'd made during the treatment.

 

All the very best,

 

 

George

User
Posted 14 Oct 2014 at 14:50

Hi Steve, Hope it goes well, it will be completed sooner than you think.  I'm sure you'll make a lot of 'new friends'  Look forward to hearing when you finish.   Arthur

User
Posted 14 Oct 2014 at 17:16

Just posted on your "cancer cluster" thread - apologies rushing as usual.

 

Hope it was okay for you today?

 

Alison

User
Posted 14 Oct 2014 at 18:55

Hope your first zapping was un eventful Steve

Bri

User
Posted 14 Oct 2014 at 20:56

Roy, George, Arthur, Alison, Bri,

Thanks for all your good luck messages. 

Yourselves and everyone on this site have helped me on my journey so far and continues to do so.

Generally, everything seemed to go well this morning.

First mistake was probably opting for an early appointment (8.30am), the traffic was terrible, but it spite of that, arrived on time.  The early time did mean that there were no delays to my appointment.

I was slightly disappointed that the waiting room atmosphere was rather sombre.  Reading posts of others who have been through this treatment, I thought it would be a lot more chatty.  It was silent.  I'll have to try and change that.  Still, very early days so far. 

Emptied my bladder, had an interview with a radiographer during which I drank my 500ml of water.  Thirty five minutes later I was stripping off my jeans, donning my gown and being lead into the treatment area.

I found the RT quite straightforward.  In some ways, because you don't feel anything, it almost seems as if you've not had anything done to you.  You just lay there, watching the equipment rotate around you occasionally, and making strange noises once in a while.  Before you know it, the radiographers are coming in and telling you you're free to go.  I nearly said "Is that it?"

Following my return to the waiting room, my first port of call, was a visit to the loo.  I could have waited longer but decided not to show off and try and drive home before going.  If I'd been caught short and had to find a loo on the way home, I wouldn't have heard the last of it from my wife (who had attended the appointment with me).

So, facing my second treatment tomorrow.  Later appointment (12.35pm) so I can have a bit of a sleep in.  Looking forward to it.

Steve

 

 

Edited by member 14 Oct 2014 at 21:23  | Reason: Not specified

User
Posted 15 Oct 2014 at 09:26

> I was slightly disappointed that the waiting room atmosphere was rather sombre

Don't worry - the mood can change depending on how many people are new, and different personality types.

Certainly I found that on same days it was fairly quiet, when on others the radiotherapists had to pry people away.

> Thirty five minutes later I was stripping off my jeans, donning my gown and being lead into the treatment area.

Maybe just Bath (or the people I was with), but men didn't seem to bother with robes - people simply strode proudly in for their session in boxer shorts from the two "feeder" changing room !

User
Posted 15 Oct 2014 at 22:33

Day Two out of the way.

The treatment is really straight forward. 

The staff are great, don't know about fellow patients yet as no one has spoken.  The waiting room was packed today but it was quieter then the local library. 

Good job I noticed there was a thirty minute delay otherwise I would have drunk my water too early and would have been suffering if I'd have to wait longer for the treatment.

Anyone considering this treatment, I'd recommend it so far, it's painless.

Onward to Day Three.

Steve

User
Posted 16 Oct 2014 at 06:18

Good to hear Steve!

 

My OH had one or two occasions that he had to 'empty the bladder' and start again if there was any sort of delay.

 

Hope the next few sessions run smoothly and you can look forward to the weekend off the RT although I expect that there are no such things as weekends off in your job!

 

Alison

User
Posted 16 Oct 2014 at 08:51
Hi,

I think I spoke to soon when I said everything was going so well.

Last night I started to notice my urine flow was very weak. Even worse this morning, it's no more than a trickle.

At the moment, I'm sat in the RT waiting room, waiting to see what's happening. They've told me to drink my water and see what happens. They're going to try to give me today's fraction, then take a urine sample to see if I have an infection. They've said it's very early to get a reaction to the RT but it does happen. Oh well, perhaps it reflects my luck recently.

Steve

Edited by member 16 Oct 2014 at 11:09  | Reason: Not specified

User
Posted 16 Oct 2014 at 16:27

Hang in there Steve, they will sort it out.

Ali x

User
Posted 17 Oct 2014 at 02:02
Hi all,

Ended up having the fraction, followed by giving a urine sample. Told to go to A&E if there were any signs that my urine flow stops completely. They think the most likely cause is an infection as it would be very unusual for me to affected this early. Anyway, they're going to see what the test shows. Meanwhile, my flow is still a slow trickle.

Not what I was expecting by day three.

Has anyone else had problems this early into the treatment?

Steve

User
Posted 17 Oct 2014 at 07:58

Hi Steve,

my flow diminished within the first week of undergoing RT.

I was put on Tamsulosin tablets for the duration of my RT and continued after.

I also was checked for infection but as non was found was put straight on the tablets.

My flow picked up after a few days and slowly took another dive as RT went on.

At one point I was on daily bladder scans post RT dosage after emptying my bladder to check for residual urine.

The final fix would be to fit a catheter but it never came to that for me.

 

I continued taking the tablets after finishing RT for around a month when my flow had returned to my normal.

I then came off them which brought back the symptoms at a lesser level. A month or so later and alls well again.

 

I'd ask to be given a treatment regime to relax the bladder neck and surrounding area.

As mentioned. I was given Tamsulosin.

 

The tablets should see you ok.

 

Best wishes

 

Kevin

User
Posted 17 Oct 2014 at 08:47

Flow was not a problem in my case but increased frequency certainly was.  It is possible that the flow was not affected because I was already taking Tamsulosin to help flow as I have a narrowed sphincter.

Barry
User
Posted 17 Oct 2014 at 14:16
Steve

sounds like your treatment has started with a bit of a bumpy ride, I think you should ask for the drugs to help your urine flow. As for people talking to you in the waiting room, Mick hd a similar experience when I was with him, however the one day I could not go with him for his chemo he got chatting straight away to the Man next to him, they stayed in touch all through his illness. It might be a case of you needing to break the silence first.

Hope things get better for you

xx

Mo

User
Posted 17 Oct 2014 at 14:37

Hi Steve,

I had problems within the first week too.

The pills mentioned by Kevin and Barry, 'TAMSULOSIN', worked well for me, although I had to take a double dose for a while half way through the 37 days. They were prescribed at the unit by my oncology nurse.

Good Luck,


George

Edited by member 17 Oct 2014 at 15:54  | Reason: Not specified

User
Posted 17 Oct 2014 at 15:27

I would also mention that RT can affect your bowels. Some men range from being very loose while at the other extreme some men - I was one of them - become constipated, possibly due to too restricted a diet. Isn't it strange how men react differently and often unpredictably to similar treatment?

Barry
User
Posted 18 Oct 2014 at 00:43

Thanks Alison, Kevin, Barry, Mo and George for your messages.

Day 4 went well, apart from the continuing very weak flow problem. I think that it must be the RT causing the problem especially with Kevin and George experiencing the same thing fairly soon into their treatment. It might have hit me hard because I'm having 3gy each day so the side effects may have kicked in a bit sooner. I hope by the time I go on Monday they might give me the Tamsulosin tablets.

The good news today was that when I arrived in the waiting room, I sat next to a guy who I'd spoken briefly to yesterday and we were joined by a couple of others, arriving for treatment who joined in the conversation.  We had quite a good chat before having to go for our sessions.  It was more like I'd expected it to be like. Only problem is my next week's appointments are at different times so I may not see the same people again for a few days. It does help to be there without my wife (she stopped attending the sessions after the first two days), because it's easier to strike up a conversation when you're by yourself.

Oh well, looking forward to next week. I quite enjoy the RT because I feel I'm doing something, at last,to beat this disease.

Have a good weekend, everyone.

Steve

Edited by member 18 Oct 2014 at 08:00  | Reason: Not specified

User
Posted 18 Oct 2014 at 14:13

Hi Steve,

Sorry that you have hit side affects so early on, hopefully if they give you the tablets on Mon this will soon sort things out. Lets hope it is plain sailing from now on.http://community.prostatecanceruk.org/editors/tiny_mce/plugins/emoticons/img/smiley-smile.gif

I know what you mean it is sometimes is easier to strike up conversation when you are on your  own. How many weeks have you got left to go?

Well the first week is under your belthttp://community.prostatecanceruk.org/editors/tiny_mce/plugins/emoticons/img/smiley-smile.gif(no pun intended)

BFN

Julie X

NEVER LAUGH AT A LIVE DRAGON
 
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