Keytruda long term effects:
I am unfortunately in the “low,” percentage of people with heavy fatigue from Keytruda. It’s getting to me. I am finishing month 5 of the therapy and I feel flat out awful: debilitating fatigue, my skin is crazy reactive to heat, had some sores start up in my mouth, etc…
Reading that there is a not insignificant chance that these are now how I feel, even after I stop taking Keytruda (hopefully)… well, like I said, it’s getting to me.
I typically power through and try not to complain. I was in the best shape of my adult life when I got the diagnosis in December 2025, and of course that’s not the case now. I feel terrible whether I work out or do anything or not, so I have at least been forcing mussels back to the gym and all the things I do normally, even if with less duration or intensity.
I am fortunate that so far, I do not have any other tumors or growths and that my testing is all still positive. I have scans coming up over summer that will show what’s up. I grateful for the fact that the cancer seems to have been managed so far.
But when I read that 96% of Keytruda users have long term effects, mostly “mild.” But that 4% have severe long term effects, I had a bit of a moment.
Just bitchin’ to save my wife from having to hear it.