Hello all! I am a new member & am 8 week's post treatment.
Besides extreme fatigue & dry mouth plus the ususal eating
issues I am not doing to bad. I have been a member for a few
day's & decided to finally jump in. However, this site seem's
very friendly & most of all helpfull. This is all new to me
& very frightening. I hope you can all bare with me as I am
computer challenged.
Roz

Stage IV Pharyngeal cancer. Treatment 38 rads 3 cisplatin

Glad you decided to break in. Ask any question and share what you want.

Welcome Roz
I know how you feel; it still feels very new to me and I'm still not sure how to manuever thru some of the forums. You will find everyone quite helpful; they will answer the most serious and the silliest questions you might have so don't be afraid to ask. Good luck!
Pat

Hi Roz, Sorry you share in this oral cancer. The worst is behind you, so enjoy getting stronger with each passing day.

Welcome to our home Rz. We are all friendly here and even mouthy at times. LOL Some like me are so full of it that it just runs out like water over a dam.

Hi and welcome Roz,
You will find this site the best for information and encouragement from the OCF family here.
Don�t worry about being computer perfect, just jump in any time you have questions or fears.
There is no such thing as a silly question or concern so ask away any time.

Thank you all! I most definitly will be picking your brain's
for information. I really do appreciate the warm wellcome.

Roz, welcome to "the family". Only a comment on being computer challenged.... when you type in the post box, you do not have to hit any returns unless you want to start a new paragraph. It is all dynamic, and your posting will shrink or expand when viewed here as the viewers screen dictates.

Welcome to OCF, Roz. You will find lots of info not just here on the forum but also on the main pages. Not all of us are computer geniuses (especially me)

I have updated the FB list and added you. The OCF website is where to go for medical info about oral cancer. Some members are also on Facebook, but thats a friend site, not for medical things. Just wanted to make sure you understood the differences. I wouldnt want to see you asking a medical question on FB and no one answering you.

Thank you kindly Christine! I really appreciate your help!

Welcome, Roz. If you have to be somewhere with this stuff, this is the place.

David 2