Wow - 2 years after diagnosis ( Diagnosed in January 2024 -G9 - T3a N0) where has the time gone! Anyway, I wanted to provide a 6 monthly update and say Hi again to the inspirational Champions who helped me so much at the start of my journey - Brian aka Millibob and Alpine Wanderer plus everyone else who I have had the "pleasure" of interacting with during this roller-coaster ride.
Have been on 3 monthly Prostap injections and now approaching my run in to completion in October 
Had my 6 monthly telephone review with one of the lovely CNS nurses who have helped me and The Rock (aka The Missus) along the way 
️ PSA now down to 0.04 ug/l with three more jabs 
to go - a long way from the 9.75 when first diagnosed.
Looking forward to more holidays in the Canaries and I`m now playing Bowls every week and also learning Spanish! So I wanted to share some positivity with everyone and give hope to those who maybe starting a similar journey and assure them they are not alone. We`ve Got This ️
Hasta Pronto - in another 6 months
FOR UPDATES ON MY JOURNEY- just click on My Profile - Activity tab - hopefully this will help others with similar diagnosis and provide some positivity on their own journey.
Wow Geoff (Geoff S)
What a brilliant, positive post - it just shows with an understanding of your diagnosis and treatment plan, a little bit of "help from my friends", Mrs Millibob is also "my Rock", and a positive attitude as you say:
"We've Got This"
Thank you for the update - enjoy the Canaries and see you in 6 months.
Kind regards - 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.
Cheers Brian and you continue to be an inspiration- keep on keeping on ️
Geoff S
We`ve Got This!
