Saying hello

Hi Casboy ( are you from Castleford) 

sorry you’ve joined the club none of us wanted to join. We’re a small friendly bunch. I had 35 radiotherapy snd 2 chrmi now 5 years post treatment. Any questions ask someone will always  try to help. 
Hazel 

Hi Casboy

All you can do is keep going...  It's a challenge but we get through it.  This is a brilliant place for support, advice and comfort.  I used the search button so often and it a topic hadn't been covered popped a question on here. 

Lisa 

Hi Casboy

Welcome to this brilliant little community ,sorry you've joined the head and beck cancer club , yes it is an emotional rollercoaster but just keep getting through each day one day at a time and no matter how crazy it may feel at times dont lose hope x

Ask any questions, drop in for a rant or an emotional outburst this lovely lot will offer you virtual hugs drinks and above all an understanding ear x

Good luck with the rest of your treatment

 Debbie

Hello Casboy  and welcome from me too. How many weeks radiotherapy are you getting and have you been offered immunotherapy?

Hi yes I'm in castleford lol

I've had 5 days radiotherapy, break now and the plan is another 5 days radiotherapy. 

But might change on Friday when I see the doc. 

I was told 10 days radiotherapy and chemotherapy for palliative care. 

Hi from me too. Sorry to be here, but this place is like a family. Always someone to be when you beed it. Guys will know if more people in here with similar experiences. Good luck with all,

marta x

Hi Casboy

Welcome, its not an easy ride but trust your team & stay strong. There is so many inspirational people you will speak to in the waiting rooms & on here that have walked in your shoes & we are here to say you can get through this. Any questions you feel embarrassed to ask there will always be someone here to help you through.

Good luck

Casboy said:

I was told 10 days radiotherapy and chemotherapy for palliative care. 

I really hope that this holds things for a while and that you have a long time with your family. Please do ask about immunotherapy. There have been some good results with lung mets. 
We have a member here who has been on Pembrolizumab for two years and is stable and I have a contact who has been on Nivolumab for five years. 
Best wishes 

Thank u for the support. 

I was told my markers wasn't right for immunotherapy