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Hormone Therapy new starter

User
Posted 17 Jan 2026 at 14:51

Hi all,


I’ve seen lots of conversations over the last 2 years which have helped me cope with this wonderful disease, so I’ve decided to jump in and ask for help and hopefully maybe help others who maybe starting out.


i was diagnosed in Feb 24 had brachytherapy in the July and it lasted about 4 months and the PSA started to rise. It’s now spread to the pelvic nodes, it is still contained. I’ve been offered cryotherapy as well drastic surgery but that maybe not the option due to risks and quality of life. I’m 57yrs PSA 4.26, Gleeson 4+4 
I’ve been offered hormone therapy tablets and injections. My question is: 


Which type/manufacturer of pills and injections come with least side effects or are they all the same. 


thank you! 

User
Posted 18 Jan 2026 at 09:03

Hi thanks for the reply


Antoinette - sounds very similar to what’s happened to me so far and I agree that they don’t understand how it affects your sex life and relationship with your partner, I don’t think they care. We are a number and a statistic.


I’ve had 3 consultations with different doctors and if I had known all the information, such as how damaged the tissue gets after brachytherapy then my decision in the beginning would have been different and I would have had the prostate removed. after these consultations I feel frustrated and have urged these doctors to ensure patients are told all the details. One of the doctors informed me that the best case scenario was we could get you to 70yrs old or there abouts,with treatment. I was glad of his honesty, but it was hard to accept. It certainly is an emotional rollercoaster.


I’ll research the ones you’ve listed so I have some idea when they prescribe it, the least side effects the better. My wife is in the menopause so she’s loving this , her words “you will know how I feel and what I go through” 🤣


thanks again!

User
Posted 18 Jan 2026 at 10:18

Hi


ive had some therapy with mental health, which has helped me cope. It’s the acceptance that this is it and there’s nothing you can do about. I’m a stubborn chap , probably like most blokes and it’s about getting your head straight and focus on living your life rather dwelling on what could happen. I’m more positive than I’ve ever been since having some help. 


the amount of pamphlets you get😲 sometimes I wish I had a wood burner 🤣


I’ve been lucky, all the nurses have been great and supportive so can’t really fault them. They’re on the end of the phone if you need them. I have heard some appalling stories and I think it depends where you live and what trusts are involved. 

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User
Posted 17 Jan 2026 at 20:11

Hi my husband was given a 4 + 4 diagnosis, after originally being told it was 3 + 3 and just to be kept an eye on. The chap we saw did say you could have another biopsy if you like. Husband said yes, and after that and a PSMA pet scan they said it was contained but one small speck in one node.  Anyway he's a fit, very active just turned 74. We also have an active sex life and both feel that is a vital part of our lives and needs to be in the equation.


He has been on Decapeptyl injections for 6 weeks. Before that he had an overlapping 4 weeks of Bicalutamide.  In his notes it says a curative path is the aim with radiotherapy after 6 months 


I have made every effort to research what will be the best for him. I did see Decapeptyl has a slightly better testosterone recovery rate, and can give slightly less side effects.


So far he hasn't had any but I do realise it's very early days. He's very active, walks a lot and did 6k paces this afternoon.  


He has got a Somaerect pump to help preserve his erections, as that can deteriorate. The cancer team just totally ignored anything we said about preserving our sex life, by phone, or the one meeting we had in person. We asked for it to be added to his notes, and it wasnt. We bought the pump ourselves, although you should get it on prescription. There is lots of advice on this forum about that.  His GP has also given him Viagra to use if he wants it. He is also on Vitamin D to help with his calcium, and his cholesterol is low.I've bought hand fans, all sorts, just in case he needs it later. 


I would say take reasonable steps to alleviate any side effects, but it seems a great many people have manageable ones, and can just take sensible steps to avoid being too uncomfortable.  If you do get side effects contact your nurse for advice ASAP. 


As far as sex life goes, apparently research suggests only 49% of men 70 + are having sex, and approximately 20% of those carry on in one form or another on ADT. Amazingly this can also depend on having a cooperative partner who's also interested.  


I think there is a younger guy on here too, called John, who chose HT and radiotherapy instead of surgery. He is a similar age and really helpful. He may answer too. 

User
Posted 17 Jan 2026 at 20:54

Hi 


It's difficult to say as there have been few head to head comparisons of the impact of different hormone therapies on quality of life.


Abiraterone seemed to do well in this recent review. 


 


https://pubmed.ncbi.nlm.nih.gov/41387022/


But other clinical factors may be important in the choice and new drugs have recently become available so best to discuss with your medical team.  It's also highly individual. I'm on enzalutamide and zoladex and have coped ok with the side effects I know others who have had worse.

User
Posted 18 Jan 2026 at 09:03

Hi thanks for the reply


Antoinette - sounds very similar to what’s happened to me so far and I agree that they don’t understand how it affects your sex life and relationship with your partner, I don’t think they care. We are a number and a statistic.


I’ve had 3 consultations with different doctors and if I had known all the information, such as how damaged the tissue gets after brachytherapy then my decision in the beginning would have been different and I would have had the prostate removed. after these consultations I feel frustrated and have urged these doctors to ensure patients are told all the details. One of the doctors informed me that the best case scenario was we could get you to 70yrs old or there abouts,with treatment. I was glad of his honesty, but it was hard to accept. It certainly is an emotional rollercoaster.


I’ll research the ones you’ve listed so I have some idea when they prescribe it, the least side effects the better. My wife is in the menopause so she’s loving this , her words “you will know how I feel and what I go through” 🤣


thanks again!

User
Posted 18 Jan 2026 at 09:06

Hi


Thank you, I’ll have look. The less symptoms the better. I take it you could switch tablets and injections if it feels you can’t cope with them?

User
Posted 18 Jan 2026 at 09:16

I would try to feel positive. 70 is a long way away for you, and they're developing new treatments all the time. Stay fit and as healthy as you can. I'm trying to persuade hubby to give up all processed meat. We've cut down but the occasional bit of bacon creeps in. 


Information helps. The cancer nurse who spoke to us afterwards was appalling. I would actually like to make a complaint, but husband doesn't want to since we may see her again. I hope not. She certainly isn't following any guidelines.  If she pushes anymore printouts from Prostatecancer.uk I shall refuse them, and say, shall we swop? Here's the guidelines for health professionals, I don't think you've read it! 


I actually thing she hates men and enjoys telling them the worst case scenarios.  Seriously. She kept telling him his body hair would disappear! 

User
Posted 18 Jan 2026 at 09:17

I don't know from experience, but others have switched and it's still effective. Ask for 1 month first to see if its OK. 

User
Posted 18 Jan 2026 at 10:05

Ok thanks 


I’ll do some research and see what I find.

User
Posted 18 Jan 2026 at 10:18

Hi


ive had some therapy with mental health, which has helped me cope. It’s the acceptance that this is it and there’s nothing you can do about. I’m a stubborn chap , probably like most blokes and it’s about getting your head straight and focus on living your life rather dwelling on what could happen. I’m more positive than I’ve ever been since having some help. 


the amount of pamphlets you get😲 sometimes I wish I had a wood burner 🤣


I’ve been lucky, all the nurses have been great and supportive so can’t really fault them. They’re on the end of the phone if you need them. I have heard some appalling stories and I think it depends where you live and what trusts are involved. 

User
Posted 02 Feb 2026 at 00:19

Hi I've just read your reply again.


I see you're 57. I wouldn't get too fixed oh his flippant " we might get you to 70" remark. There is this magic 10 year survival tally. In fact 10 years new protocols and medication may be out, and people who have had the latest testament 5 or 7 years ago, haven't even got to 10 years or longer yet so they aren't in the statistics. 


I afraid I have a completely different experience to your wife: I didn't even notice the menopause at 54 at all. I had no idea I was so fortunate. I had no hot flushes, no weird moods, my brain's definitely not foggy, and my libido is as high as it always was. 

 
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