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Welcome to the NETs Group! Come say hi.
Neuroendocrine Tumors (NETs) | Last Active: 2 days ago | Replies (410)Comment receiving replies
Hello @netpatient and welcome to Mayo Clinic Connect. I am happy to have you posting in our NET discussion. Have you personally been diagnosed with NETs or perhaps a family member?
At the University of Michigan, there are doctors who perform surgery, I'm sure if you called them you could find a surgeon or an oncologist for treatment of metastasis.
As you just started posting, please feel free to share more information, as you feel comfortable doing so. Would you share about your history with NETs and how you are feeling?
Replies to "Hello @netpatient and welcome to Mayo Clinic Connect. I am happy to have you posting in..."
Thanks again. Can you help with University of Michigan hospital link or email or phone or contact.
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Hello at hopeful33250, I am the patient. I was diagnosed in 2018/19 though I had known about this tumor for about 2 decades. Possibly existed longer than that. After metastasis, NET damaged my bones.. Though I have shrinked my tumor by about 50% now. My damaged bones is my greatest priority but the existence of the tumor is still a threat. Can you help me with Michigan hospital contact. I need medical help/care.