← Return to Anyone have neuroendocrine tumor (NETs) of the breast?

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@trixie1313

@pamelasantacruz
I'm just over 5 years now since diagnosis, chemo, radiation, and two surgeries (lumpectomy for first tumor and second for further excision of the first and the second tumor found on MRI which turned out to be NET). I've recouped from all and, so far, so good. For a while there I was having to have PET scans every 3 months as some oddities showed up in my lungs but we're now at yearly PET scans. I was advised to take aromatase inhibitors which I did for 5 year and I was encouraged to go an additional 2 years, but quite frankly I just couldn't do the extra 2 years and my body and mind are doing much better without it! My motto is just enjoy one day at a time to the fullest. All the best to you.

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Replies to "@pamelasantacruz I'm just over 5 years now since diagnosis, chemo, radiation, and two surgeries (lumpectomy for..."

I’m loathe to take hormone blockers, I will learn more Wednesday. If ai must I will but side effects sound terrible. Thank you Teixie, it sounds like you are doing well and that’s so good to hear. x