MORE INFORMATION

PATIENT ORGANISATION

The Sarah Jennifer Knott Foundation is a patient organisation in Ireland and provides helpful information about CUP for patients, their families, friends, and carers.

 

The letters S, J and K, standing for Sarah Jennifer Knott Foundation, appear in a handwritten font. There is a stylised flower emblem next to the letters.

 

HOW TO TELL FAMILY AND FRIENDS

It can be quite difficult to find the right words to explain what CUP is. Many people know about cancer, but they often do not understand that the primary tumour cannot be found.

It may be helpful to first explain the terms “primary tumour” and “secondary tumour” (metastases); then to explain that for CUP, only the secondary tumour can be found. Reasons why the primary cancer cannot be found are listed here.

ARE MY CHILDREN AT RISK OF CANCER?

CUP itself is not known to have a specific risk of being inherited. However, some people are more prone to develop cancer than others. DNA plays a central role in cancer evolution. Since a part of your DNA is passed on to your children, it could be possible that your children may be at risk of developing cancer. Please discuss your individual situation with your doctor. He will also tell you if a consultation with a human geneticist may be needed.

SUPPORTING DOCUMENT

This document is designed to support CUP patients in their cancer journey. It contains examples of topics patients may want to discuss with the doctor and some helpful ideas for the next visit to the doctor.
DOWNLOAD SUPPORTING MATERIAL

FURTHER WEBPAGES DEALING WITH “CANCER”

More detailed information on cancer may be provided by the following webpages (please note: the current webpage does not take responsibility for the content of external webpages):

UK Cancer Research Institute

American National Institute of Health

American Cancer Society

Deutsches Krebsforschungszentrum

 

YOU ARE NOT ALONE!

Patient organisations might help you get to know other people in the same situation.

LIVING WITH CUP

You may wish to ask your medical specialists where you can find further information about how to manage life with CUP, e.g., what to consider in terms of nutrition, exercise, psychological or social support.