There is always hope.

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Hi everyone,

It has been a while since I last posted on this forum but I occasionally drop in to have a look and familiarise myself with current posts. I thought it was time to share what might be considered good news for those families who have been recently affected by this horrible and indiscriminate disease. I was diagnosed on 9th March 2020 with stage 4 Prostate cancer which had spread to my bones in various locations, lung & lymph nodes. I was prescribed Abiraterone + Prednisolone along with 12 weekly Prostap3 hormone injections, which I am still on to this day. My PSA dropped to less than 0.1 (undetectable) and has been the same since mid June 2020. I had a meeting with my consultant last week and she is delighted with my continued results, so if she is happy, I am certainly happy.

What I`m actually saying to anyone who has been recently diagnosed with PC or even anyone on active treatment, please do not give up hope!!  I am 6 years down the line which I didn`t think I would get, being positive does help.

I wish you & your families all the best on your difficult journey ahead. Stay strong & take care.

Tom (HarleyD) 

  • Evening  Tom (HarleyD) Thank you for writing that it does give everyone hope, my husband was diagnosed 2024 with extensive bone mets he is on triplet therapy and is just about to change to tablets instead of injections because of a heart attack. He is still working at home and enjoying life. 

    All the best to you Sheena 

  • Hi Tom, that’s exactly the kind of reassurance I have been looking for. I was diagnosed with stage 4 two weeks ago and have just started hormone treatment. I have zero pain in my affected bones and feel physically strong. Mentally it’s been difficult but reading your post and other excellent contributors on here has given me hope and convinced me it’s a condition that you can live with for many many years. 

    Many thanks and best wishes for the future. 

  • Good Evening Tom ( 

    Cracking post and thank you for returning to give hope and encouragement to other members of our little band of brothers (and sisters).

    I know we all have to jump through hoops and ring bells to get to where you are but in the end it's worth it.

    I wish you many more years with an undetectable PSA - please do keep coming back every 6 years to share your good news.

    Kind regards - Brian.

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