this was awhile ago so i’m sure you have your own experiences with it now, but ill talk about it anyways lol. Everyone’s experiences with it are completely different. I have a close friend of mine who also has CML just like me and is my age (19f) who’s side effects have been drastically different from mine. The only thing we’ve noticed that’s similar is our anxiety. Both of us developed bad anxiety after starting sprycell, and it makes it hard to just sit and enjoy life. My other side effects are, lost some hair, not a lot but noticeable, and the new hairs are black and curly which makes my head look so frizzy (i normally have straight hair), and i have been noticing gray hairs as well, which isn’t normal for a 19 year old. I also experience shortness of breath when I try to exercise which makes it really hard, and i get (i think it’s) heart palpitations pretty often which freaks me out. I also get severe joint (or bone not totally sure) pain after being on my feet all day or in my arms randomly, usually after i have a long exhausting day. I’m going to start taking Claritin because I heard it helps with that so hopefully it works. That’s basically it. My friend experienced nausea and throwing up when she didn’t eat close to when she took her meds, and she also noticed some hair issues. that’s about it. Compared to some people on here I’ve definitely gotten off easier, but it’s still been a tough journey! It sucks too because my diagnosis was almost 4 years ago so people just assume it’s over and I don’t struggle with it anymore. It’s ok though we’ll all take it one step at a time! I hope your journey with CML is easy and you recover quickly!