Prostate cancer

ive been given a date for mry prostatectomy 11th november so hopefully be picking up by christmas.good luck everyone going through some shit.
All the very best pal, on top of the other stuff going on I am having a tumour removed from my neck on the same day at MRI,.Good luck to us both.
 
ive been given a date for mry prostatectomy 11th november so hopefully be picking up by christmas.good luck everyone going through some shit.

All the very best pal, on top of the other stuff going on I am having a tumour removed from my neck on the same day at MRI,.Good luck to us both.
Best of luck to you both. Keep on posting in here.
 
Unfortunately we’ve received the news this week after my latest round of blood tests we’ve sadly not beaten this my cancer is still here and growing, I’m now with the Christie and will have to go under a quite intense session of radiotherapy, it’s devastating news especially for my wife and girls who have been through too much already, but we’ll fight and then fight again until we’ve beaten it .I’m in a minority who doesn’t beat this dreadful disease first time round so please don’t give up in thinking it’s all doom and gloom if you are unfortunate to have it , I’ve lost a war but the battle will be won .
Up the blues .


Please lads get checked .
I had my PSA results today at the Christie as it’s six months on from my radiotherapy and we’re so pleased it’s back down to 0.1 psa.
A huge relief it looks like they were bang on target with the radiotherapy, after the prostectomy then 18 months later to need the radiotherapy it’s been a long road and now I’m finally looking at the light at the end of the tunnel. Go back in 6 months for repeat psa tests then hopefully go in remission again, for the family it’s such relief they’ve been through enough especially my two daughters, emotional day to be honest.
So goes without saying a big thank you to each and everyone of you in your support for not just myself but others who are going through this dreadful disease.
As I’ve said before we’re in this together and we will keep going !!!!
We will carry each other through this .

It’s sometimes said city fans have no class well I beg any visitors on this site to go through this thread you will come back with a different view I guarantee it.

Ladies and Gentlemen you are the best of the best , sorry for the late post it’s been a long day for us.

Good Luck to all on here dealing with this we keep going ,

Gary.
 
I had my PSA results today at the Christie as it’s six months on from my radiotherapy and we’re so pleased it’s back down to 0.1 psa.
A huge relief it looks like they were bang on target with the radiotherapy, after the prostectomy then 18 months later to need the radiotherapy it’s been a long road and now I’m finally looking at the light at the end of the tunnel. Go back in 6 months for repeat psa tests then hopefully go in remission again, for the family it’s such relief they’ve been through enough especially my two daughters, emotional day to be honest.
So goes without saying a big thank you to each and everyone of you in your support for not just myself but others who are going through this dreadful disease.
As I’ve said before we’re in this together and we will keep going !!!!
We will carry each other through this .

It’s sometimes said city fans have no class well I beg any visitors on this site to go through this thread you will come back with a different view I guarantee it.

Ladies and Gentlemen you are the best of the best , sorry for the late post it’s been a long day for us.

Good Luck to all on here dealing with this we keep going ,

Gary.
Great new, the very best wishes to you A57 and your family.
 
I had my PSA results today at the Christie as it’s six months on from my radiotherapy and we’re so pleased it’s back down to 0.1 psa.
A huge relief it looks like they were bang on target with the radiotherapy, after the prostectomy then 18 months later to need the radiotherapy it’s been a long road and now I’m finally looking at the light at the end of the tunnel. Go back in 6 months for repeat psa tests then hopefully go in remission again, for the family it’s such relief they’ve been through enough especially my two daughters, emotional day to be honest.
So goes without saying a big thank you to each and everyone of you in your support for not just myself but others who are going through this dreadful disease.
As I’ve said before we’re in this together and we will keep going !!!!
We will carry each other through this .

It’s sometimes said city fans have no class well I beg any visitors on this site to go through this thread you will come back with a different view I guarantee it.

Ladies and Gentlemen you are the best of the best , sorry for the late post it’s been a long day for us.

Good Luck to all on here dealing with this we keep going ,

Gary.
Great news Gary...the bold bit is to remind yourself that you've been through quite a bit as well mate, don't forget that. Though I suspect you are similar to me...just get on with it.
 
Great news Gary...the bold bit is to remind yourself that you've been through quite a bit as well mate, don't forget that. Though I suspect you are similar to me...just get on with it.
Thanks Bob I appreciate the reply mate,
I was sat in work on Sunday reading your posts on the Sir Chris Hoy thread inspirational Bob , and yes I think sometimes even when inside we’re struggling mentally and physically it was important to let the family see routine and normality as much as possible.
The very best to you mate and keep your spirits and strength high.
 
I had my PSA results today at the Christie as it’s six months on from my radiotherapy and we’re so pleased it’s back down to 0.1 psa.
A huge relief it looks like they were bang on target with the radiotherapy, after the prostectomy then 18 months later to need the radiotherapy it’s been a long road and now I’m finally looking at the light at the end of the tunnel. Go back in 6 months for repeat psa tests then hopefully go in remission again, for the family it’s such relief they’ve been through enough especially my two daughters, emotional day to be honest.
So goes without saying a big thank you to each and everyone of you in your support for not just myself but others who are going through this dreadful disease.
As I’ve said before we’re in this together and we will keep going !!!!
We will carry each other through this .

It’s sometimes said city fans have no class well I beg any visitors on this site to go through this thread you will come back with a different view I guarantee it.

Ladies and Gentlemen you are the best of the best , sorry for the late post it’s been a long day for us.

Good Luck to all on here dealing with this we keep going ,

Gary.

Sounds good news thank God. I have been testing since 2014 as my PSA was high. I've had a biopsy and four scans over the years because my levels have been up and down. Thankfully they have been okay. It's an ongoing thing. Good luck to everybody facing this awful disease and other ones.
 
I had my PSA results today at the Christie as it’s six months on from my radiotherapy and we’re so pleased it’s back down to 0.1 psa.
A huge relief it looks like they were bang on target with the radiotherapy, after the prostectomy then 18 months later to need the radiotherapy it’s been a long road and now I’m finally looking at the light at the end of the tunnel. Go back in 6 months for repeat psa tests then hopefully go in remission again, for the family it’s such relief they’ve been through enough especially my two daughters, emotional day to be honest.
So goes without saying a big thank you to each and everyone of you in your support for not just myself but others who are going through this dreadful disease.
As I’ve said before we’re in this together and we will keep going !!!!
We will carry each other through this .

It’s sometimes said city fans have no class well I beg any visitors on this site to go through this thread you will come back with a different view I guarantee it.

Ladies and Gentlemen you are the best of the best , sorry for the late post it’s been a long day for us.

Good Luck to all on here dealing with this we keep going ,

Gary.
Me and Kath so pleased to hear this news Gary

PM me or give us a bell if you up for another meet up in Glossop could do a away game again in the Cupboard
 
I had my PSA results today at the Christie as it’s six months on from my radiotherapy and we’re so pleased it’s back down to 0.1 psa.
A huge relief it looks like they were bang on target with the radiotherapy, after the prostectomy then 18 months later to need the radiotherapy it’s been a long road and now I’m finally looking at the light at the end of the tunnel. Go back in 6 months for repeat psa tests then hopefully go in remission again, for the family it’s such relief they’ve been through enough especially my two daughters, emotional day to be honest.
So goes without saying a big thank you to each and everyone of you in your support for not just myself but others who are going through this dreadful disease.
As I’ve said before we’re in this together and we will keep going !!!!
We will carry each other through this .

It’s sometimes said city fans have no class well I beg any visitors on this site to go through this thread you will come back with a different view I guarantee it.

Ladies and Gentlemen you are the best of the best , sorry for the late post it’s been a long day for us.

Good Luck to all on here dealing with this we keep going ,

Gary.
so pleased to hear this mate all the best for the future
 
I had my PSA results today at the Christie as it’s six months on from my radiotherapy and we’re so pleased it’s back down to 0.1 psa.
A huge relief it looks like they were bang on target with the radiotherapy, after the prostectomy then 18 months later to need the radiotherapy it’s been a long road and now I’m finally looking at the light at the end of the tunnel. Go back in 6 months for repeat psa tests then hopefully go in remission again, for the family it’s such relief they’ve been through enough especially my two daughters, emotional day to be honest.
So goes without saying a big thank you to each and everyone of you in your support for not just myself but others who are going through this dreadful disease.
As I’ve said before we’re in this together and we will keep going !!!!
We will carry each other through this .

It’s sometimes said city fans have no class well I beg any visitors on this site to go through this thread you will come back with a different view I guarantee it.

Ladies and Gentlemen you are the best of the best , sorry for the late post it’s been a long day for us.

Good Luck to all on here dealing with this we keep going ,

Gary.
Great news Gary, really pleased for you and your family.
 
I had my PSA results today at the Christie as it’s six months on from my radiotherapy and we’re so pleased it’s back down to 0.1 psa.
A huge relief it looks like they were bang on target with the radiotherapy, after the prostectomy then 18 months later to need the radiotherapy it’s been a long road and now I’m finally looking at the light at the end of the tunnel. Go back in 6 months for repeat psa tests then hopefully go in remission again, for the family it’s such relief they’ve been through enough especially my two daughters, emotional day to be honest.
So goes without saying a big thank you to each and everyone of you in your support for not just myself but others who are going through this dreadful disease.
As I’ve said before we’re in this together and we will keep going !!!!
We will carry each other through this .

It’s sometimes said city fans have no class well I beg any visitors on this site to go through this thread you will come back with a different view I guarantee it.

Ladies and Gentlemen you are the best of the best , sorry for the late post it’s been a long day for us.

Good Luck to all on here dealing with this we keep going ,

Gary.
Great news mate so pleased for you and family
 
I had my PSA results today at the Christie as it’s six months on from my radiotherapy and we’re so pleased it’s back down to 0.1 psa.
A huge relief it looks like they were bang on target with the radiotherapy, after the prostectomy then 18 months later to need the radiotherapy it’s been a long road and now I’m finally looking at the light at the end of the tunnel. Go back in 6 months for repeat psa tests then hopefully go in remission again, for the family it’s such relief they’ve been through enough especially my two daughters, emotional day to be honest.
So goes without saying a big thank you to each and everyone of you in your support for not just myself but others who are going through this dreadful disease.
As I’ve said before we’re in this together and we will keep going !!!!
We will carry each other through this .

It’s sometimes said city fans have no class well I beg any visitors on this site to go through this thread you will come back with a different view I guarantee it.

Ladies and Gentlemen you are the best of the best , sorry for the late post it’s been a long day for us.

Good Luck to all on here dealing with this we keep going ,

Gary.
Brilliant news mate, stay strong blue you got this ;)
 
I had my PSA results today at the Christie as it’s six months on from my radiotherapy and we’re so pleased it’s back down to 0.1 psa.
A huge relief it looks like they were bang on target with the radiotherapy, after the prostectomy then 18 months later to need the radiotherapy it’s been a long road and now I’m finally looking at the light at the end of the tunnel. Go back in 6 months for repeat psa tests then hopefully go in remission again, for the family it’s such relief they’ve been through enough especially my two daughters, emotional day to be honest.
So goes without saying a big thank you to each and everyone of you in your support for not just myself but others who are going through this dreadful disease.
As I’ve said before we’re in this together and we will keep going !!!!
We will carry each other through this .

It’s sometimes said city fans have no class well I beg any visitors on this site to go through this thread you will come back with a different view I guarantee it.

Ladies and Gentlemen you are the best of the best , sorry for the late post it’s been a long day for us.

Good Luck to all on here dealing with this we keep going ,

Gary.
Nice one Gary! Really pleased for you.
 
Or have a brother/father/uncle with the the fucking thing. Although we shouldn't have to.
Don’t say cousin like me I was told too far removed.? I now have two cousins with bowel cancer. Make the relationship as close as you can some things are too precious.
 
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I had my PSA results today at the Christie as it’s six months on from my radiotherapy and we’re so pleased it’s back down to 0.1 psa.
A huge relief it looks like they were bang on target with the radiotherapy, after the prostectomy then 18 months later to need the radiotherapy it’s been a long road and now I’m finally looking at the light at the end of the tunnel. Go back in 6 months for repeat psa tests then hopefully go in remission again, for the family it’s such relief they’ve been through enough especially my two daughters, emotional day to be honest.
So goes without saying a big thank you to each and everyone of you in your support for not just myself but others who are going through this dreadful disease.
As I’ve said before we’re in this together and we will keep going !!!!
We will carry each other through this .

It’s sometimes said city fans have no class well I beg any visitors on this site to go through this thread you will come back with a different view I guarantee it.

Ladies and Gentlemen you are the best of the best , sorry for the late post it’s been a long day for us.

Good Luck to all on here dealing with this we keep going ,

Gary.

Hi Gary, I’m glad to hear you have had good news. I wouldn’t have know anything about this thread until I searched. I’ve had a problem urinating every hour ish been for a MRI scan and been told they have found lesions. Going in for a biopsy on 8th November. I thought the hourly urination was part of my diabetes. This is to tell anyone who has problems with a change of the frequency in urination to GET IT CHECK OUT PROMPTLY.
 
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I had my PSA results today at the Christie as it’s six months on from my radiotherapy and we’re so pleased it’s back down to 0.1 psa.
A huge relief it looks like they were bang on target with the radiotherapy, after the prostectomy then 18 months later to need the radiotherapy it’s been a long road and now I’m finally looking at the light at the end of the tunnel. Go back in 6 months for repeat psa tests then hopefully go in remission again, for the family it’s such relief they’ve been through enough especially my two daughters, emotional day to be honest.
So goes without saying a big thank you to each and everyone of you in your support for not just myself but others who are going through this dreadful disease.
As I’ve said before we’re in this together and we will keep going !!!!
We will carry each other through this .

It’s sometimes said city fans have no class well I beg any visitors on this site to go through this thread you will come back with a different view I guarantee it.

Ladies and Gentlemen you are the best of the best , sorry for the late post it’s been a long day for us.

Good Luck to all on here dealing with this we keep going ,

Gary.
Wow!! That’s fantastic news mate. Really happy for you & your family.
 

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