This website is intended for an international audience, excluding the UK, United States, Canada and France
This website is intended for an international audience, excluding the UK, United States, Canada and France

There are a number of NET support groups that give you and your family a chance to share your experiences with other families.

Contacting other people with NETs through these support groups may help you to learn new ways of coping with the changes that may occur after you are diagnosed with neuroendocrine cancer.

These groups can also provide you with further information on specific topics of interest within a supportive environment.

Some groups also have patient forums on the Internet for people with NETs and their carers to share ideas, concerns and tips about living with NETs.

Helen, Living with NETs

“Try and join a local patient association. You will make friends who understand you, get good advice, and receive reliable information about NETs including updates on recent research and activities to help people living with NETs.”

View Helen’s story >

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This website is intended for an international audience, excluding the UK, United States, Canada and France. This website has been developed by Ipsen in collaboration with those living with NETs and the healthcare professionals who care for them. Ipsen would like to thank everyone for their valuable insights and stories. All names used on this website are not necessarily real names. Visit www.ipsen.com for more information about us. Website design and development by Kanga Health Ltd. ALL-ALL-002300/November 2020