Any NET patients from NYC

Posted by Laurell @laurell410, Mar 22, 2022

Looking to connect with patients diagnosed with NET in NYC

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

@colleenyoung

@laurell410, you'll notice that I removed your personal contact information from your post above. We recommend sharing personal contact information using the secure private message function rather than in the public forum.

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Thank you

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@hopeful33250

Hello @sophiarose ,

It is a!ways a good idea to seek a second opinion. How are you feeling? Are you able to eat, do you have much fatigue or pain?

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I have my good and bad days
Yes I can eat I try to eat small meals because if I overdo I get diarrhea
The fatigue is bad but I have no pain

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@sophiarose

I have my good and bad days
Yes I can eat I try to eat small meals because if I overdo I get diarrhea
The fatigue is bad but I have no pain

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@sophiarose

I would love to hear from you again. Will you post again after your appointment at Sloan?

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Hey girl! How are you doing?

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