Just diagnosed stage 4. Thankyou so much. Beautiful soul.😊👍

Thank you so much for that video. I appreciate it all the more because I know how much it will have taken out of you. My condolences on the loss of your wife - she clearly meant a great deal to you. My experience with radiation and ADT has been very similar to yours, and like you my physically active life has rather slumped into a porridge. I wish you all the best for the future.

Well done for having the courage to talk about your personal circumstances. Thank you. All the best.

Thank you for being open and sharing your experience, especially to a bunch strangers. I'll be 50 in a couple of years and will take this knowledge forwards. My deepest condolences for your loss this year. And well done for reaching the milestone of over 100 subscribers, me being one.

Thanks you for sharing. It's very timely for me, as tomorrow I have an appointment with my GP. I'm in my 60s, so I really should get this checked.

Thank you ... the push I needed. I'll call the Health Centre tomorrow to ask for a test. I hope you keep well.

Thank you for sharing your story. I agree with the concept of valuing health span over lifespan--it really is about quality of life, not quantity. Best wishes for the next steps of your journey to be more positive and rewarding!!!

Appreciate the candid discussion, the more this happens the more likely it is that awareness will improve. My father is stage 4 so this video touched home, his current treatment is palliative (hormone therapy) and we've had 2 years or so since initial diagnosis which has been welcome, but this year his PSA has shot up (>100) and we're probably looking the final stages of this disease. Wishing you well with the channel, everyone starts with zero so congratulations on your first 100 (it's 99 when I'm typing this so only a matter of time).

Thanks so much for sharing your story. You might feel weak at times but your strength comes through on your videos. You are a natural at this and it's brilliant to see you finding a passion. Would love to follow you along on this journey and your new exciting EV journey! You should do a video on how you ended up living in France!

I watched a couple of your posts on your Niro EV recently as I too have owned and enjoyed EV’s for nearly four years. I then noticed this post. Thank you so much for being so candid and courageous about recounting your prostate cancer history. I was diagnosed with advanced stage prostate cancer about six weeks ago and have been on hormone therapy (tablets followed by the regular injections) since then. I am due to have radiotherapy in a few month’s time. I am uncertain what will happen after that but understand it’s possible I will need to continue on the hormone treatment at least for some time. Your story was very helpful for me to hear, including about the various side effects, which I sort of knew about. It’s early days for me but I have particularly noticed the tiredness affecting me a little. However, I do thank you again for sharing your experience with everyone and wish you all the best, whichever way you decide to go with your continued treatment and also for your KZfaq channel. I will definitely continue to watch your posts and have now subscribed. Thank you also for sharing details of the Maggie Centres, which I’d not heard of and I will look into further.

Very brave of you to talk about this to your subscribers. But as you say if at least one person decides to get checked out and catches it sooner you have done a great job there 👍 All the best to you and your future.

I have had serious gut pain im 64, 3 months now 2 months ago pain was so bad mainly when i lay down , or after even small meals, anyways i went to have tested they admitted me my white cell count was very high, Dr thought a stomach or urinary infection,put me on antibiotics, i got no relief,still sharp gut pain, my PSA was 1.2. Had another blood' test in 30 days boom 74 ? They think prostate cancer, im not rushing to nothing, infections can and do raise PSA , so do viruses, im not going to let my treatment destroy my quality of life, the pain is still with me, not as often ,as i fast many hours,and eat only perfect food, 0 sugar,no carbs, keto style, healthy fats protein, nutrients dense veg, after watching many men's stories i may refuse all treatment, try control pain ,and just keep it natural, i dont fear death, i worse fear being a lump in a chair too long, i ask you when and what treatment helped the gut pain for you ?

Very informative indeed, thank you for the video. Hormone treatment is brutal, I've been on it for six months, have gained 2st and 6" on my waistline, lost body hair, feet swell, ED the lot, it's pretty miserable really but it could be worse of course. I found I had PC through a routine blood test (9.2), biopsy (ouch), found to be Gleason 7 (4+3) stage T3A which means the cancer is just outside my prostate. After my test, my three older brothers had blood tests and all were found to have PC too, so you can guess on the topic when we get together. Four brothers with varying degrees of PC on various treatments. Back to ADT treatment, or let's call it what it really is, "chemical castration", I can fully understand why anyone would consider stopping hormone treatment (ADT), you have to be enduring it to fully understand. Gents, please have a regular PSA test if you are over 50, note that myself and my three older brothers had no symptoms of PC. One word of advice for people on ADT, exercise is KEY, I lift weights four times a day and walk a couple of miles each day, althouth it's getting more difficult to walk due to muscle loss, which is another side effect. Luckily I have a physical job and I'm sure that helps although I'm finding it more tiring. Apologies for the long rant

I've been enjoying your e-Niro videos. Sorry to hear about your wife and your health. I see a nice guitar in the background any chance of a tune in a future video? 🎸🎷

Thank you so much for sharing your experience., is not easy to go through all this ordeal.

Thanks for sharing. Good luck with your treatment and with your EV adventures. Cheers from Gippsland Australia.

Many thanks for posting this. It is a nudge to me to get checked. You see so much conflicting information, but I think the main thing is to establish a baseline from which you can see the direction of travel. I am so sorry you didn't turn over the page on your first blood test, but we are where we are. I am surrounded by old geezers such as myself, and they all seem to know their numbers, as do my older and younger brothers. Thank you for another kick up the arse. I hope your energy levels improve. If you do come off drug therapies, I would urge you to take a look at fasting as a means of at least slowing the progress of the disease. I was an avid follower of Dr Michael Mosley (until his recent untimely demise) and he often promoted the many benefits of fasting. Keep up the channel. You touch on many interesting things, such as living in France. Perhaps you could talk about that occasionally? I am writing this from our little gaff in Portugal which we have had for ten years. We live in Sheffield, though, and that is now home. But I lived in Torphichen, near Bathgate, for six years, and love Scotland. I digress. Keep doing what you're doing, and thanks for the boot up the backside.

63 and on active survalence, had blood test done initially because I felt I had low testosterone and my doc advised I had my prostrate checked as well, testosterone came back normal but PEA was 7, had scan done and pirads came back at 4, which was red light, had biopsy, 18 taken two found to be slightly cancerous, no cancer in my family, never smoked, fitness fanatic all my life, I was scared and really really angry, got to have another PSA next month, who knows what's around the corner, sorry about your wife, you seem like a nice chap, thanks for your vid.

I share your condition having been diagnosed late last year. Am doing what is called Active surveillance at the age of 67. Told best to get the prostate removed before I reach 70.

Well said sir and thank you, yes maggies is so good one guy called hormone (adt) treatment advance devils treatment very effective as you say but its the quality of life thats important aswell, i to have many of your symptoms after being on it for 18 months, bless you all on the pc journey.

Is your Maggie Center located in Edinburgh? We are considering moving there next year, as diplomats. I have stage 4 metastatic, have done radiation, chemo (which was bad but short and doable; great results I think) and now ADT with injections and enzalutamide. We are trying to assess if Edinburgh would have the infrastructure to support a move there. Any help would be appreciated.