Recently diagnosed and in lots of ways very lucky as I have got it early.
However I am trying to work through the choices and I think have narrowed down to permanent seed brachytherapy or surgery and take it all out, I think. Completely overwhelmed at the moment and work are being dicks so just looking for some similar stories really..
Anybody here gone through the seeding process.
just saw your post and wanted to wish you well on whatever journey you decide to go down . It’s mind boggling but someone on here will give you support . My OH is in HT/RT so can’t advise .
take care & hugs
Liz & OH xx
A sad welcome, but all is not lost, your Urologist and Oncologyst will offer advice and guidance. I cannot have mine removed as I am high risk of return, so hormone and radiotherapy, I am good with that, even though it would have been my choice for removal.
The advice, other people's journey, will be extremely beneficial. I also advise, one hurdle at a time and patience.
All the best to you on your journey.
Hi Stanlee66bd5e
Welcome to the group. Lots of knowledgeable people on here can help with any questions you may have.
Diagnosis is a whirlwind for everyone, but things get easier once you've sorted out what you want to do and are on a treatment path. You are right, catching it early is great news and makes a complete cure highly likely.
I went down the surgery path as I was looking for a quick result and am happy with my choice. Feel free to ask me anything. I'm sure someone will be along shortly to tell you about their Brachy experiences.
PC is very slow growing so take your time considering the various options.
Best of luck
Cliff
Thanks Cliff, My first instinct was surgery but not sure I could deal psychologically with the potential side effects.
Hi Stanlee...
Sorry that you have had to join this group but you will find it a brilliant source of help & information.
You say that work are being dicks which is a great shame given the situation you now find yourself in, but are you aware that The Equality Act (if you are in England, Scotland or Wales - Disability Discrimination Act still applies in N. Ireland) considers a diagnosis of cancer as a disability which gives you important rights. Might be worth looking into what sort of help this might be to you if needed.
Best Wishes
Brian
Hi Stanlee66bd5e - yes, I have. Check out my bio & ask any questions. You may only need brachytherapy without wider radiotherapy. AW
Sorry to hear mate
I was diagnosed in March , also 3+4 , spent months looking at options including focal but ended up going for full surgery which is next week but got to be honest the surgeon I met via the NHS gave me no confidence whatsoever so if he had been the only choice I would have taken another treatment option , I eventually searched for high volume surgeons with good outcomes and reviews and nave paid for it privately, if you do look at surgery don’t be pushed into the first one that is offered as I believe you can ask to be referred to others , I was always told to look at someone who does at least a 100 procedures a year
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2025 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007