Having just finished my immunotherapy after 2 years on Pembrolizumab. I was also told that after 2 years it can do more harm than good. I am due to speak to my oncologist regarding the most recent CT scan on the 1st Nov 2021 then again a review of treatment on the 9th November. I like everyone else the treatment has giving good results and I have felt the same as before I was diagnosed . I must admit, now it has stopped you feel that you are being written off. I know this is not the case, and I'm sure and hope the oncologist reassures me when I speak to her. What is crazy I don't feel any different to before I was diagnosed. Because I have a belt and braces GP, he sent me for a chest X-ray because I has a nagging pain behind my ribs. No cough, no real pain.... and hey presto... comes back with stage4 lung cancer . The reason for my post, is just to reassure those who want to know what happens at the end of treatment. I should know in the next 2 weeks, so if you don't mind I will keep you posted
Finally, does anyone else avoid watching things like stand up to cancer, storylines in soaps or when a celebrity dies of cancer you check to see which one it is.... or is it just me. It's like I disassociate my self from it... I guess because nothing has changed yet with any real health issues, just in my head.
Sorry if this sounds like rambling.... because it likely is.
