Carcinoid syndrome: Video, Causes, & Meaning | Osmosis
Carcinoid syndrome: Video, Causes, & Meaning | Osmosis
143.4K viewsJan 5, 2018
osmosis.org
What are some nutrition tips for people living with carcinoid syndrome? Bonnie Bennett, Nurse Coordinator for the Neuroendocrine Tumor Program at the University of Pennsylvania, and Beth Leonard, a patient, explain more in this short clip from "Do You Have Carcinoid Syndrome? Talking with Your Healthcare Provider About Symptoms, Diet, and Treatment." Watch the full program here: https://www.carcinoid.org/treatment-education/ Living with Neuroendocrine Cancer | Neuroendocrine Cancer Foundation
1:22
What are some nutrition tips for people living with carcinoid syndrome? Bonnie Bennett, Nurse Coordinator for the Neuroendocrine Tumor Program at the University of Pennsylvania, and Beth Leonard, a patient, explain more in this short clip from "Do You Have Carcinoid Syndrome? Talking with Your Healthcare Provider About Symptoms, Diet, and Treatment." Watch the full program here: https://www.carcinoid.org/treatment-education/ Living with Neuroendocrine Cancer | Neuroendocrine Cancer Foundation
5.1K viewsNov 30, 2018
FacebookNeuroendocrine Cancer Foundation
What are the signs and symptoms of Carcinoid Syndrome? NET expert Dr. David Metz explains in this short clip from Do You Have Carcinoid Syndrome? Talking with Your Healthcare Provider About Symptoms, Diet, and Treatment. Watch the full program here: https://www.carcinoid.org/treatment-education/ | Neuroendocrine Cancer Foundation
1:37
What are the signs and symptoms of Carcinoid Syndrome? NET expert Dr. David Metz explains in this short clip from Do You Have Carcinoid Syndrome? Talking with Your Healthcare Provider About Symptoms, Diet, and Treatment. Watch the full program here: https://www.carcinoid.org/treatment-education/ | Neuroendocrine Cancer Foundation
3.3K viewsNov 1, 2018
FacebookNeuroendocrine Cancer Foundation
Meet Beth who has two primary neuroendocrine tumors, carcinoid syndrome, and Lynch Syndrome -- she is truly among the rarest of NET patients! Here's why Beth uses the Carcinoid NETs Health Storylines app to manage her health. https://healthstorylines.com/blog/?page_id=476 Living with Neuroendocrine Cancer | Neuroendocrine Cancer Foundation
2:24
Meet Beth who has two primary neuroendocrine tumors, carcinoid syndrome, and Lynch Syndrome -- she is truly among the rarest of NET patients! Here's why Beth uses the Carcinoid NETs Health Storylines app to manage her health. https://healthstorylines.com/blog/?page_id=476 Living with Neuroendocrine Cancer | Neuroendocrine Cancer Foundation
3K viewsApr 9, 2019
FacebookNeuroendocrine Cancer Foundation
Shock was Dana's first reaction when she was diagnosed at age 31 with neuroendocrine tumors throughout her body. Her boyfriend couldn't cope with her diagnosis and Dana found herself alone, her world turned upside down. And then came Brien . . . | Neuroendocrine Cancer Foundation
6:10
Shock was Dana's first reaction when she was diagnosed at age 31 with neuroendocrine tumors throughout her body. Her boyfriend couldn't cope with her diagnosis and Dana found herself alone, her world turned upside down. And then came Brien . . . | Neuroendocrine Cancer Foundation
19.3K viewsSep 18, 2018
FacebookNeuroendocrine Cancer Foundation
Cancer Research
Cancer Research
Jan 1, 2009
cancer.gov
Neuroendocrine tumor (NET) guidelines are an important resource for both physicians and patients. Assembled by a group of experts, guidelines provide up-to-date, standard-of-care information about diagnosing and treating people living with NETs. Especially important for rare cancers, guidelines afford community physicians, who may have limited experience treating rare disease patients, a place to access the most recent algorithms for treating patients. For patients, guidelines help them to bette
5:24
Neuroendocrine tumor (NET) guidelines are an important resource for both physicians and patients. Assembled by a group of experts, guidelines provide up-to-date, standard-of-care information about diagnosing and treating people living with NETs. Especially important for rare cancers, guidelines afford community physicians, who may have limited experience treating rare disease patients, a place to access the most recent algorithms for treating patients. For patients, guidelines help them to bette
2.3K viewsOct 9, 2020
FacebookNeuroendocrine Cancer Foundation
7:23
The Carcinoid Cancer Foundation teamed up with The Balancing Act and Advanced Accelerator Applications to raise awareness about carcinoid and neuroendocrine tumors (NETs) during a feature on Lifetime TV on February 28, 2017 (Rare Disease Day) and March 8. Behind the Mystery: Rare and Genetic Diseases features Judy Golz, a carcinoid patient sharing her story; and Matthew Kulke, MD, Director of the Program in Neuroendocrine and Carcinoid Tumors at Dana-Farber Cancer Institute and Professor of Medi
10.7K viewsNov 26, 2017
FacebookNeuroendocrine Cancer Foundation
All About Cancer
Jan 19, 2017
cancer.org
6:43
Mark was only 11 years old when he was diagnosed with lung neuroendocrine cancer. Here's how life changed for this husband and dad who is now in his thirties. | Neuroendocrine Cancer Foundation
14.6K viewsDec 12, 2018
FacebookNeuroendocrine Cancer Foundation
CancerCare | Free Support Services to Anyone Affected By Cancer
Sep 26, 2013
cancercare.org
16:01
In March 2020, Randall made a decision he never made in decades as a family doctor in Woodstock, NY: he called 911. What seemed like a routine case of pneumonia turned into an accidental discovery—something hiding in his pancreas that one one was looking for. Days later, he was in surgery. The next day, New York City shut down for COVID. And the results that came after? They changed everything. But that wasn’t the end of the story… years later, it came back, faster than anyone expected. Through
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FacebookNeuroendocrine Cancer Foundation
Donate to Cancer Council | Cancer Council Australia
Jul 20, 2020
cancer.org.au
1:20
We share the stories of neuroendocrine tumor, patients and how they navigate different aspects of life with this rare cancer. You can see Jesi's full story on our Facebook page. #NeuroendocrineCancer #NeuroendocrineTumor #rarecancer #LetsTalkAboutNETs | Neuroendocrine Cancer Foundation
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FacebookNeuroendocrine Cancer Foundation
2:39
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Apply for Grants | Cancer Research Institute
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Markey Cancer Center
May 6, 2024
uky.edu
18:13
In 2020, Ilka had just made her son Shane her healthcare proxy. Admittedly, he wasn't prepared to fill that role at his age. But just one year later, it became necessary... Ilka was diagnosed with a neuroendocrine tumor, a rare cancer that often goes misdiagnosed or undiagnosed. But with the right community, support, and specialists, it can be managed in ways that give patients the best chance at maintaining their quality of life. Shane and Ilka are in this fight together. This is their story. |
7.1K views8 months ago
FacebookNeuroendocrine Cancer Foundation
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Cancer Research in the US Is World Class Because of Its Broad Base of Funding
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