Prostate cancer

[TShed]

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

 

[city saint]

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

 

[RobMCFC]

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.

 

[ob]

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

 

[burnley blue mcfc]

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 ;)

 

[DenisLawBackHeel74]

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.

 

[A57 the snake]

Nice one Gary! Really pleased for you.

Thanks mate appreciate it ,
Thank you.

 

[Kirkstall Blue]

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.

 

[r.soleofsalford]

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.

 

[Manc baggie]

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.