Hi
just got the devastating news that my pet scan picked up one bone metastasis in my spine at L3 . I was diagnosed in September with aggressive cancer psa 50 but that time scan showed no bone mets only lymph node & prostate spread . The plan was chemo to shrink tumor & rT as curative intent . But now this bone met the rt dose will be palliative rather than curative . I am going for another mri to make sure it’s a met and not degeneration Bcos psa has fallen down significantly with chemo plus size of prostate & the lymph nodes have almost disappeared! So doesn’t make sense how spread to bone happened
would be reassuring to know how many of you out there have bone mets and how long you have had it ?? Just terrified if I am gone in like 6 months ! I am just 49
I have advanced prostrate cancer diagnosed in July 2021. I'm on Hormone therapy and doing fine. I was told 5 to 7 years on current treatment but research for new treatment is moving fast. There will be many more on this forum who can offer some long term positive stories. I don't think this is necessarily a death sentence anymore.
Hi,
I've been on 12 week Zoladex jabs since May 2020, with virtually no side effects, (I was Gleason 9). Maybe I'm lucky, but PC is not a death sentence anymore! My PSA is fairly constant at around 1 sopleased all round. I'm told I'll be on HT for life, but hey, if it keeps me going I'm happy!
So keep positive everyone, and best wishes to all.
Lots. I really don't know. I find low impact gym work and cycling easy and have no pain. Walking long distances will get slightly painful and I noticed pain yesterday whilst digging. I have my first follow up later this week so I'm going to ask for more information on bone mets and how the drugs will manage them .
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