NET in the jejunum spread to liver
Hi Everyone,
Has anyone had an NET that originated in the jejunum (small intestine) that has spread to liver? If so, I am wondering how your doctor handled? My husband has received this diagnosis and we are wondering about surgical options. He is taking a monthly injection, and has a CT scan done once a quarter.
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
My family as well as myself are praying for the same results! Thank you so much for sharing your story….
@dbamos1945, thank you so much for sharing your story. I am very thankful to hear the treatments are working well and pray that will continue. I am going to share this, and Vinnie’s story with my husband.
Yes surgery dissection for my liver isn’t an option for me.
Yes I’m on the Lanreotide injection every 28 days. I started February 10th 2021.