Welcome to the carcinoid syndrome blog

You’re in the right place for articles, news, and information on NETs and carcinoid syndrome.

Updated monthly, this blog is a place to get information on NETs and carcinoid syndrome, from the perspectives of real patients, caregivers, doctors and other health professionals in the community.

Check below to find our latest article, or scroll down to explore articles from previous months

Patient Education on Carcinoid Syndrome from Diagnosis to Treatment June 27, 2017

On March 1, 2017 Cancer Coach Live in cooperation with the Carcinoid Cancer Foundation held a live program focused on carcinoid syndrome. The event featured NET cancer expert Edward M. Wolin, MD; CCF Chief Operating Officer Grace Goldstein; and patients Mitch Berger, Giovanna Imbesi, and Rick Mainwaring. Watch this discussion about best practices in diagnosis and treatment.

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Welcome to the Place for Education and Support Resources on Carcinoid Syndrome June 26, 2017

The Carcinoid Cancer Foundation and its generous partners are excited to introduce the Carcinoid Syndrome website. This website is a space for news and education on carcinoid syndrome, along with information on neuroendocrine tumors (also known as carcinoid cancer). We believe this site will be a great resource for patients, caregivers, and physicians alike – looking to learn more about carcinoid syndrome.

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