At one point it was 56 ,that’s when they diagnosed me metastatic to the ribs . With medication it went down over time in 3 years it went down to a 9 . Every 2 months I’m tested, it seems to be creeping back up . 9 then 11 now 13 . I’m scared . I know under 32 is within normal ranges but to be 9 and now 13 ? Has this happened to anyone else? Any advice please 🥰thank you in advance .
My CA 15-3 is rising slowly, I’m scared - SHARE Metastatic ...
My CA 15-3 is rising slowly, I’m scared
Everything about this disease is scary. Most scary is the not knowing, the writing for results, the the specter of progression, the losses. What helps me about tumor markers is that some docs don't follow them at all. What matters about your numbers is that they are Small numbers. Talk to your doc about this. Never hesitate to get a second opinion.Wish you the best.
Actually when I was diagnosed with MBC to the bone both of CA ‘s were low and normal as if I don’t have any problems! So those are not reliable factors and my onc doesn’t check it anymore Sima
I started MBC 5 years ago at 60 the lowest was 32 now I’m 160. Just has a CT scan and they’re not seeing anything so TBH that’s fine by me. Just trying to eat healthy and maintain a positive attitude. One day at a time!
I will do what you said and eat healthier, you are so kind to write , I only wish the best for all of us . Ty for responding always ❤️🙏🌹💕🥰💐
This is reassuring- my tumour marker is jumping exponentially again, am awaiting CT (nz too poor for petCTs usually!) And hoping my fulvestrant/palbo hasn't stopped working cos I feel otherwise well!
I would be so happy with those numbers. I was 445 on initial diagnosis and when things went haywire they rose to 5,500. I’m now at 415.
My wife has had CA15-3 from 90 up to 200, just coming down to 150 and we were delighted with that, try not to stress, those are still very good numbers, we'd be delighted with those! I hope that makes you feel better. XXX ❤️