Hi
My name's Lee and I'm 54. I was diagnosed with advanced prostate cancer in February 2026. The year before I went to my GP and raised concerns that I thought I might have cancer due to lower back and abdominal pain. I wasn't offered a PSA test. Instead the doctor did blood tests for liver function because I told him I was club/ rave DJ in the 90s and 00s and I used to drink most weekends socially. I was told if I didn't hear anything in two weeks after blood tests I was ok and was also sent a link for lower back pain by surgery and told to get some over the counter Codeine.
Fast forward a year and I started to suffer from serious urinary issues. I then contacted surgery and requested a PSA test myself (wasn't seen by a doctor). Test came back at 49. Then had every scan under the sun and was diagnosed with advanced prostate cancer covering 80 percent of my prostate. It has also spread to my pelvic bones.
I started my treatment a few months ago. I am on the new triple therapy programme and chemo session number 3 is this coming Monday.
My diagnosis turned my life upside down. I have my family to talk to but I am a single man, I live alone and my beautiful 11 year old daughter comes to stay with me every weekend.
I find everyday a struggle now. Mentally even more so than the physical side of things. But somehow I manage to get through each day and I'm just getting on with life the best I can.
I'm fortunate to have my hobby, making electronic dance music and spending the weekends with my daughter is the one thing that keeps me going.
I decided to join the group and share my story after reading about several other men who are in a very similar situation and would definitely understand where I'm at and what I'm going through.
So hello everybody and if you would like to know anymore about my story please do not hesitate to ask me. And I welcome any tips anybody has on how to cope with being diagnosed and the treatment that goes with it.
Hello Lee (String )
A warm welcome to the group although I am so sorry to read of your journey so far - we all arrive here with a story to tell, however yours shows how inept your GP was!
Triplet therapy is fairly new however group members who have had it all appear to be doing well with low PSA results so you look to be in good hands - especially if the spread is only to the pelvic bones.
I have picked up on the fact you are single and struggling mentally - and yes I can understand why as you don't have a big support network - can I suggest the following ideas? (Well I will anyway!).
* Do you have a Maggie's at your hospital? - this is a cancer charity where you can just drop in - have a chat over a brew and get some help.
* Are you aware of Macmillan Buddies.? if you sign up we can allocate you with a "buddy" who will call you every week for a chat - it can be about cancer, the price of fish or Rave music in the 90's (no boom boom shake the room please ) the link is there.
* There's Andys Man Club for local mental health support. They meet once a week.
* Don't forget our support line on 0808 808 00 00 (8am to 8pm 7 days a week) - they can offer support too.
We are all open on the group so please do continue to post. Some of us have our own story to read and you can do this by clicking on our name or avatar.
If you wish to add your personal journey to your profile on your home page, click on the computer screen, top right, then profile, then edit - once you have written something remember to save it.
We all have our own coping mechanism - mine is the cancer won't define me and I am going to enjoy life, and carry on.
Best wishes - Brian.

Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm
Strength, Courage, Faith, Hope, Defiance, VICTORY.
I am a Macmillan volunteer.
Thanks for your reply Brian, much appreciated and some excellent advice on things that may help with me coping with my diagnosis, I will look into all the things you have suggested in the next week or so.
As for my GP, I consider their treatment, or lack of, which is more appropriate, as negligent and I am currently going through the official complaint procedure with my surgery.
I will indeed continue to post as my treatment progresses to let you know how things are going. I had a meeting with my oncologist yesterday and my PSA has dropped from 49 to 0.8. She said this is really good considering I've only had 2 cycles of chemo so far. Hopefully the treatment will continue to go well.
Hi Graham, thanks for your reply. At last someone who understands as I have also had many days and nights early on in my diagnosis when I didn't want to be here anymore. I have kind of come to a point where I have almost accepted where I'm at but things will never be quiet the same again. I have also like you however been coping quiet well with my treatment so far, fingers crossed it continues. Thank you for taking the time to reply and much love goes out to you and your family and your cockapoo. Best wishes for the future.
Hello Lee (String )
Cracking PSA result and I am pleased all is well - as for you GP - good luck with that and I hope you get somewhere - if only to help others who come after you.
Give me a shout if you need anything else or just want a chat - happy to help.
Best wishes - Brian.

Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm
Strength, Courage, Faith, Hope, Defiance, VICTORY.
I am a Macmillan volunteer.
Yes thank you Brian, yesterdays meeting was in fact very very positive, something my life has been seriously lacking since diagnosis. As for my complaint I will keep you updated on how that proceeds. And thanks for your kind offer of support, I will definitely bear that in mind. I am looking forward to getting Monday's cycle over and done with as that means I'm half way through. I will post an update on how it's all going next week.
There are many more like us, keep the faith, stay strong, despite your shaky start there are some excellent medical experts who will help you overcome this in the short , medium and even long term as new treatments are developed and become available for likes of us. All the best
Thanks Graham, my shaky start has been a long hard slog to be honest and still ongoing. I have good days and really bad days. I'm impressed how you seem to be coping with it all. Maybe I should take a leaf out of your book and try being stronger if only for my daughter. Hopefully I will get to that point eventually, all I can do now is try my best I suppose.
Hello Lee (String),
I'm fast approaching 70 and was first diagnosed with PC in 2016. Unfortunately it recurred in 2024 and I was put on triplet therapy. I'm coming up to 2 years since completion of chemo and my 12 weekly checks continue to show undetectable PSA so all's well.
I began writing a blog when I started triplet therapy and, if you're interested, there's a link below to have a read. I got through 5 of the 6 docetaxel infusions, the 6th was cancelled due to side effects - but this was complicated by the fact that I'd had different chemo for a different cancer in 2014 and, believe it or not, my consultant told me I was still affected by that which made my docetaxel side effects much worse.
I'm very sorry you're struggling, but things will definitely improve in time. Although my path is not what I expected, I'm living life to the max.. Currently in south west USA and will be celebrating, with my wife, my big birthday next week in our favourite city of Tucson, Arizona.
I wish you all the best for successful and event free completion of chemo. If there's anything you want to ask feel free.
Derek.

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