NET so worried

Posted by catherinemary @catherinemary, 1 day ago

So pleased to have found this discussion group for NET patients. Can’t post atm but looking forward to very soon. Cheers

Interested in more discussions like this? Go to the Neuroendocrine Tumors (NETs) Support Group.

Hello @catherinemary and welcome to the NETs support group on Mayo Connect. I hope you will share more about your journey with NETs. As you do so, I'll help you to connect with other members in our NET group who are in a similar place.

I have had three surgeries for NETs, over the past 21 years, in the upper digestive tract. The only treatments I have needed are surgeries.

Is this a new diagnosis for you? Would you be able to share where your NET is located? I look forward to hearing from you again.

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Hello Teresa, and thank you for your words of welcome. I am about to leave home for a short time however I will give a rundown of what’s been happening over the past few months a bit later today. Thank you, Cathy

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Good morning! Still very very anxious about my appt with a medical oncologist at the Royal Brisbane and Women’s Hospital tomorrow. The oncologist at ICON cancer (a private group practice) made this appt for me.
Cheers, Cathy

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@catherinemary

Good morning! Still very very anxious about my appt with a medical oncologist at the Royal Brisbane and Women’s Hospital tomorrow. The oncologist at ICON cancer (a private group practice) made this appt for me.
Cheers, Cathy

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Good thoughts go with you as go to this appointment, @catherinemary. Here is a link to a discussion, "Keys to a Successful Doctor's Appointment" that might help you to navigate the first meeting with the oncologist.
https://connect.mayoclinic.org/discussion/keys-to-a-successful-doctors-appointment/
Will you post again and let me know how you are doing?

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