HI all,
I'm just a few days from the end of my 28 HT tablets (Bicalutamide 50mg) and had my first injection (Decapeptyl SR 3.75mg) two weeks in and looking at the sheet I was given (and a copy for the Dr) it looks like my next injection, 30 days after the first could be 'Prostrap 11.25mg' OR 'Decapeptyl SR 11.25' and my Dr Surgery has put Prostrap on my medications list.
Two questions please.
Why would the Drs allocate the Prostrap over Decapeptyl, other that was on the top of the 'OR' list and
it says on the form that this second injection should be administered '3 monthly' but has previously stated 1 monthly?
So does it go, 14 days tablets, injection, 14 days tablets, stop tablets, 14 days later 2nd injection, then ... injections every 3 months till ... ?
Also, there is no mention of when I start RT and / or what other tests I might have / need along the way? Is there a set time or is it based on say my PSA etc please?
p.s. I went to the second PC monthly meeting and it was good to see all the guys, plus a few extras again. One chap commented that I seemed much happier this time. ;-)
waiting lists are on the up and it's common to wait for over 6 months nowHow does that impact the outcome OOI Brian?
For got to add, I have a telephone consultation with Oncology in a couple of days so I can ask then.
Waiting for a few extra months for RT shouldn't affect the outcome as the HT will have stopped the cancer growing.
Hi able, HT is given to stop your production of testosterone which is what cancer needs to feed on, your PSA number indicates how well the HT is working. your oncology team will give your HT time to have maximum. effect. The better HT works, the lower your PSA the better it is for the radiographers and you. I do not know any of your stats but most people wait at least 6 months for RT. I am pleased you have joined a prosttate support group, the macmillan community is wonderful but there is nothing like being with people face to face who are on the same journey, I have been on mine for 18 months, i do 2 groups. have counciing, do a little fundraising, help out at the hospice and am starting 2 alternative therapy groups soon. I can guess it is all new, overwhelming and frightening but if you have anything you want to talk about you know where we are, please take care.
I am pleased you have joined a prosttate support group
As am I. It was actually quite interesting (well, and sad also) to not be the 'new boy', even only on the second meeting and to be better positioned myself to be able to add some bits here and there in support of the others.
I think the issue for me is / was more the thought of the surgery than having the PC!
No, I was offered both with the exact same predicted outcome after 5 years (95% survival rate or some such), initially went for surgery based only on the idea that you could have RT after surgery easier than the other way round, but bottled it the day before my surgery and so rather than the rock, took the only other sensible option, the hard place.
So wouldn't say I've chosen RT, it's just that I didn't choose surgery and was encouraged to choose something (positive). ;-)
I'm now just in 'the machine' and will have to wait and see what comes out at the other end (if there can ever be 'an end' with this disease etc).
Morning Able You can always start a journal of your personal journey through Prostate Cancer - it helps others understand where you have been and where you are going. (You can read my 22 months by clicking on the image of the beach next to my name).
To do this just follow the first 3 instructions on "how to upload a profile picture", It just saves answering the same questions sometimes and gives new Community members an idea of what to expect.
Oh - I've had a few "issues" on the way but don't expect all those on your HT/RT journey - it will be like a walk in the park!
Best wishes - Brian.

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Hi Able, Sadly i am unable to offer any advice on surgery as my heart and anaesthetic do not get along, As for RT I think most of the guys on here have been down that route in combination with HT. As millibob suggests a personal journal will help others to support you, and later on your journal will almost certainly help others. RT+HT can bring side effects so other peoples experiences will help you prepare and manage any you may get. take care.
Hi Brian,
I took the telephone appointment call from the RT Dr earlier and it looks like I am due to have a PSA test at a week short of 3 months (from my next RT injection?) and subject to that result, start the RT.
I also got more explanation re the initial smaller dose of HT. I though it was a lower dose as a test to check if I reacted badly and I was sort of right. Apparently it was only a one_month_dose, the idea being if there were bad side effects, they would only last a month, not the 3 of the 'std' dose?
I really think I would like to have sat down with someone one_to_one and had them go through it all from initial diagnosis (raised PSA) to the rehab so that I had a clearer picture of it all.
I'm not someone who would absorb such information reading it, not only because I know I wouldn't bother to, but the chances are it wouldn't be interactive enough as I couldn't further question anything along the way.
I can still re-iterate word for word the explanation of the whole PSA <> Prostate <> reproduction system given to me by the first consultant I met in this process. He put it across in a form that was perfect for me, so it's not just a matter of remembering, but understanding (at least understanding that particular version of the facts). ;-)
Hello Able
Well that's happy days RT is on the way. Before you get your dates for the 20 fractions you will attend a "planning scan" where they will check you over, tell you how it works and give you your tattoo's.
It's a good job my first dose of Hormones didn't give me any reaction as the banged a full 6 months worth of hormones into my backside in one go!!
Best wishes - Brian.

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