Neuroendocrine Tumour

FormerMember
FormerMember
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Hi. Im new to this forum. My husband was diagnosed bout 2 months ago witn a NET in the small bowel. They said it was size of a mandarin orange. However progress seems to me to be very slow. He has just been for nuclear medicine scan. App he now needs a biopsy to stage and grade. Has anyone else been thru likewise. Tyia x

  • Morning Joden, are you in the right group if the cancer is in his bowel? Or does he also have a tumour in his osophagus?

    The process for when my cancer was found was I had an endoscopy because I was struggling to swallow. During this they found my tumour as they found the lump they took a biopsy there and then. About a week later I had a CT scan and then a further week later a PET scan. After that I met my oncologist another week later and they come up with a treatment plan. I don't know the process for bowel cancer people in that group will be able to give better advice as the journey and side effects can be very different.

  • FormerMember
    FormerMember

    Hi Joden, 

    NETs - neuroendocrine tumours are a different cancer to the others- it’s rarer. There’s a fab group on fb - neuroendocrine tumour uk support - many people in there who have had NETs in the small bowel. They’re very friendly so pop over and they’ll be able to help you. Xx