NETWise Episode 1: What You Need to Know About NETs.
6,960
2020-02-19に共有
To download a copy of the transcript for this episode:
netrf.org/podcast/what-you-need-to-know-about-nets…
To listen to other NETWise episodes:
netrf.org/podcast/
NETWise is a podcast featuring neuroendocrine cancer experts and patients, produced by the Neuroendocrine Tumor Research Foundation (NETRF) in Boston, MA, USA.
コメント (11)
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Thank you for this great video!! I was diagnosed with small bowel NET in July of 2020. I have lymph node involvement in the mesentery and a small mesenteric tumor. (localized mets). A PET scan done in October 2020 after I had healed from the small bowel resection showed no additional metastasis. Praise God!! A follow up CT of the abdomen and pelvis done in July 2021 (my one year anniversary) also showed no additional metastatic spread!! Again Praise God!! Thank you for such a great informative video!!! God Bless!!
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I was just diagnosed 3 days ago with a NET to my Ileum. Waiting now to be seen by a physician to discuss my treatment options. This was a very informative video. Thank you
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The main problem with diagnosis is doctors are trained to think the patient is lying if things do not add up for them. Doctors should be health detectives. I am a PNet, misdiagnosed for over 20 years. My Neuroendocrine Cancer was not found till after it atrophied my pancreas. It is a crime what NET patients have to go through to get good care.
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My husband had a net tumor recently removed from his bladder. Nothing I read about this made sense and no one seemed able to tell us more than it was an aggressive type. Thankfully I found this series. It explains simply but thourghly and answered many of our questions/that can be.
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This information on NET is so interesting and I understand my problems better. Thank you. I got tumors in my liver and still been treated with Sandostatin successfully for 3 years now . I don't for how long I'm going to get the injection '
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Thank you for this series. I am finding it very helpful and informative.
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It's just a picture but you are thru what you are saying
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By chance I was DX in October 2022, mine can’t be operated on and hot flash are my worst side effect, I get a special injection to help this but is being changed to every three weeks. Another is lower extremity weakness. Godbless caregivers and patients.
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Some doctors do not listen to patient's symptoms. They always say "We go by the book. Do not believe things you read on the internet" (I explained I have the same symptom as described by CDC website) As it turned out, the hospital misdiagnosed me. 3 doctors! Some drs always think they know more about the patient's body than the patient himself/herself.
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It's just a picture but you are thru what you are saying