New to the group

Hi John. A warm welcome to our little community. Sorry you have to be a member of our elite club but as you’re here it’s good to have you. There are a few of you NP sufferers, one just starting the trip so I hope you can stick around with some words of wisdom. 
So pleased  you are recovering. Long may it continue. 
All the best 

Thank you for the warm welcome dani 

Means a lot 

I'll stick around

Just noticed what a cool avatar you have.

Hi John and welcome to the forum! although i am sorry you had to join.

That is a lot of chemo! glad to hear you got through it mostly ok, and yes it changes us (i am 1 year younger than you and never imagined this)

Let us know how your recovery gets on please!

Trev

Hi John

welcome to the club that none of us want to join. Am sure your input will be invaluable as each of us are  different yet the same. 
Almost a year since diagnosis and treatment  all  through covid as well 

Onwards n upwards 

Hazel x

Me and my dog

I. Never imagined it either 

It presented itself as sinutitus

Then quickly escalated to the point I couldn't breathe out of my nose at all

That was scary 

Recovery is slow but sure 

Taste returning 

Saliva not 

I'm. Back at work 6 months after treatment 

That was a good milstonee for me. 

It's been a battle. 

The covid situation has made it tougher 

And in some ways easier 

My wife never got to. See me crying in the last week of radio

She's seen enough pain ️

You got through and well done.  It’s bloody awful what the radiologists do to us. But hey. They manage to fix us 

Hi John and welcome!  Glad you got through the treatment.  You advice to people following in your footsteps will be invaluable.