As I mentioned in my previous post, we are a group pf patients and caregivers. Please remember we do not have your medical history in front of us, medical training or text book experience. Our knowledge comes from living thru oral cancer (OC) diagnosis, treatments and recovery experiencing everything first hand.
In the US our physicians adhere to the NCCN flow chart to aid them in their treatment plans. I do not know what is done in other countries. What you described for your treatment plan sounds like what many of us here have been thru. Please take some time to read some valuable info with both the link below and the links in my previous post above.
Ive also sent you a private message (PM). click on the tiny flashing envelope next to the My Stuff tab. There an important link there to review too. Please use the link to follow the directions about adding a signature. It really is important in helping us to help you.
NCCN treatment plans for head and neck cancers Best wishes!
