I am just being diagnosed with SCC. So far they have only done biopsies in mouth, throat and tongue looking for the primary. They did find the primary behind the tongue last wednesday and lasered. I have been in such pain that not being able to swallow that I am so scared for what is ahead..

I go back today to find out more.. Any words would help..

thank you
elle

It's impossible to not be at least a little frightened. You will find a lot of support here and a lot of sucess stories!!!

Good Luck!

Elle,

What lies ahead is a fight for your life. Without knowing more, it's hard to say how hard that fight will be, and I sincerely hope for yours to be among the less difficult of those you will find here. You will do it though, no matter how hard it is. You will find that strength within, as we all have.

You will find help here with any and all questions, worries, and problems along the way. Please write in when you know more about your future plan of attack. We'll be here to help wherever and whenever we can.

Lani

Wow it seems like so long ago yet just the other day I was sitting in your chair. I went to the oral surgeon by myself cause everybody was too busy to go. When he told me that he was sure it was cancer and was going to book a biopsy all I could say is I can't do this....It can't be...I can't do this...wow I got to the car and the tears started coming... felt so alone and despondant...Well Elle here I am today a suvivor had extensive surgery and terriefied was the word for my journey and fight...It is not going to be easy but you can do it and there will be someone with you every step of the way. The hardest part of all this is waiting and you will hear it many times the fear of the unknown. I learned to trust in my family here on the OCF site and my doctors. I did not find this site till after my biopsy and waiting for the results. I found it through my team at the hospital doing my cancer treatment. It has been such a help to me and many others. Please do not hesitate to write. You will come out of this a winner one step at a time

Don't be afraid to ask for second and third opinions...also take yourself to a cancer center if you can. They have more people that work with cancer pt's.
Lots of real good info here. Ask questions of your Dr and the folks here and try to keep yourself informed. We've all walked in your shoes or next to them so we know where you are.
Best of luck

Thank you everyone who responded to my cry for "help."

Direction and help is there for the asking and taking :))

We're here, Elle. We ALL remember being in your shoes! Each of us has traveled a different path, but we all have that initial terror in common.....and we're all here now, comforting each other and helping newbies. You've come to the right place for either information or just comfort. You are free to ask, or to rant, or to cry or to celebrate! We appreciate it all, and we've done it all. Keep us posted.....and stay close!

XO--Colleen

elle,

As soon as you find out more, come back and post what they said and we will be able to give you loads of info. Until then try to relax. Also tell us a little more about yourself. See everyone's Signature Line as an example.

I have been diagnosed with squamous cell carcinoma on the right floor of mouth/tongue. I had surgery to remove as well as a follow-up of radiation and followin that, chemo therapy. During radiation I had a sever flare-up and had to stop the IMRT treatment. It was resumed and I concluded the treatment.

My question is if re-radiation of this same area, especially the head and neck, is possible and if so, how many times has this been done before. My understanding was that when you had radiation you cannot reradiate the same part over again? it is true?
Sofar my doctors has suggested IMRT, stereotactical radiation, proton treatment and I have difficulty deciding which would be the best, could you let me know your opinion?

Thank you for your help.
pino