← Return to Neuroendocrine carcinoma

Discussion
movetowellness avatar

Neuroendocrine carcinoma

Neuroendocrine Tumors (NETs) | Last Active: Sep 14 9:11am | Replies (13)

Comment receiving replies
Profile picture for Teresa, Volunteer Mentor @hopeful33250

Hello @denisepierce and welcome to Connect. I am glad that you found this forum. NETs are a rare form of cancer, and it helps to meet with others who are travelling down the same road. I came to Connect before my third surgery for NETs in the upper digestive tract. I had no symptoms to indicate that there were any problems; it simply showed up in an upper endoscopy.

Share, as you would like, a bit about your journey with NETs. How long ago were you diagnosed? Was your large cell neuroendocrine carcinoma located in the digestive tract?

I look forward to hearing from you again.

Jump to this post


Replies to "Hello @denisepierce and welcome to Connect. I am glad that you found this forum. NETs are..."

I was diagnosed with non small cell carcinoma, they removed part of lung, then diagnosed with large cell carcinoma cells, I took chemo but it showed up again, took radiation that shrunk the tumor. Now doing ct scans to monitor.