Welcome to the NETs Group! Come say hi.
Hello and welcome
Let's pull up our chairs in a circle and check in with each other and talk about how we are doing with our NET diagnosis. Any new tests, meds or treatments going on for you? What about your symptom control? Any concerns you have?
Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.
Hi! Pavlina here, 62 yo. Accidental CT scan of my chest discovered a mass in my abdomen in December. 16 cm mass on the tail of my pancreas. Multiple tests later I am going to a surgery on Feb.1. I will have a Ga dototate PET scan on Jan.26 hoping not to see spreading. Preparing for the worst, hoping for the best and leaning in God's hands.🙏
Prayers for you
59 yr diagnosed with Pheochromocytoma or paraganglioma. The doctors are trying to find somewhere that does an MIBG scan, so they can see where it is located.
Adrenal glands where clear on CT scan.
Not much information on metastasis I guess it’s a wait and see. I’m bit nervous.
After reading about others on here I feel fortunate at this time. Sending all my prayers and positive energy to all of you.
I was wondering if anyone has had this tumor and what was that like in the treatment of it.
Thank you so much! This is a beautifully curated discussion group. This was discovered 5 months ago. I did indeed consult with a neuroendocrine specialist (University of NM), and the pathology was also confirmed with Mayo. Every doctor I've consulted has specified: 6 months of chemo, lumpectomy, 30 radiation treatments, and long term aromatase-inhibitor. However, I have kidney disease, a missing lung, and numerous co-morbities. I decided against chemo and targeted therapies, and was told I had 1-2 years to live. So I settled into that, working on quality of life. Now the tumor is responding well to the AI and my surgeon is very optimistic about possible curative rather than palliative effects of forthcoming lumpectomy. Obviously a roller coaster! There is almost no info on survival rates–in the only study anyone could find the participants all died too quickly for any kind of outcome. I'm resigned to not "knowing" and proceeding in an authentic manner, but it has been baffling.
I appreciate hearing from you again. How great that the tumor is responding to the treatment and that the lumpectomy might possibly be curative.
Yes, this has been a roller coaster ride for you. When you say, "I'm resigned to not "knowing" and proceeding in an authentic manner, but it has been baffling" I can understand that. You have had a lot of opinions and it is good to hear that you are accepting of where you are and how you will conduct yourself during the ups and downs of this process.
As you are having six months of chemo, how far into that six months are you now?
Hello and those are the best hands to be in right now. Blessings to you as you go forward .
Carcinoid Specialists in The Villages
I live in The Villages. I am looking for a Carcinoid Specialist here. Can anyone recommend someone?
He offered an injection that will help with symptoms. Because she isn’t able to do the scan he recommended she start hospice. She wants to talk to another oncologist in our town. She is really tired and in going to work on getting her affairs in order. She has an appointment with her internist and endocrinologist on Monday.
I'm glad to hear that she wants to see another oncologist.
You mentioned that the doctor wants to give her an injection. Did the doctor indicate that the injection was octreotide?
It is lanreotide.