Post treatment blues
Hi all
I think I am turning into a hypochondriac. I am 3 and a half months post chemo and 5 weeks post radiation. Right through treatment, I was managing well with minimum side effects. And through treatment, I have avoided reading up on the statistics or detailed pathology reports but followed my drs advice and guidance on treatment.
I thought that having such positivity, I would be able to handle understanding the details now that the hospital treatments are over. So guess what, I went online to find more information. From what I read, it is getting to me....having a rarer type (pleomorphic) of lobular (I also have a idc), being er-pr+ (again very rare) etc.....
So now every ache and pain or anything, my mind just want to think the worst.....eg.would femara work on er- since it is a estrogen blocker? I have since saw my onco. The other day I had 2 white lumps on my tonsils and it send me into a tailspin until the gp said it was tonsil stones and they are now gone. Had a CT to check on 2 pre-treatment tiny nodules in lungs and showed up nothing. It sure does not take much.
Most days I am good. Physically, I am fit and well except for some minor aches, and have kept up my walking exercise.
Sorry, just have to write it down and have a bit of a whinge. I am looking forward to being less anxious about things (knowing it makes no difference) and live a life as well as I can. Thanks all for reading.
Hope you all are travelling well.