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PNET removed 2 years ago: Can it come back at another site?
Neuroendocrine Tumors (NETs) | Last Active: Aug 5 3:18pm | Replies (31)Comment receiving replies
Wow!!! That is so wonderful to hear! That is the longest I have heard of. It's so nich for long term survivors to post on these boards to give others hope. It took me a long time to realize that long term patients and survivors aren't as active on these boards because they've done so well and have moved on. As a result, we tend to hear more of the short term stories.
Thank you amd co grats to your pioneering Mom!
Replies to "Wow!!! That is so wonderful to hear! That is the longest I have heard of. It's..."
I had my 1.2 cm removed. It spread which was not expected. It had spread to one lymph node. 9 were removed. No treatment at this point. Scans every 6 months for 5 years. And yes I tend to not comment as I think I’m doing very well compared to others. All the very best to everyone!!
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Thank you so much! It’s my pleasure to help others have HOPE because hope is sometimes all cancer patients have. And it really does help the body heal in so many ways! I hope you and your husband look into The Seena Magowitz Foundation so I can meet you both in person someday. All survivors are welcome and the CEO, Roger Magowitz reads everyone’s story and personally welcomes you.