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Home > renal survey

CEAPIR RENAL SURVEY 2011

Do renal patients receive the required information to make an informed choice?

CEAPIR is working to reduce the burden of renal disease on both the individual and society. Its mission is to improve the quality of life of people with renal disabilities in Europe. In 2006, CEAPIR published the results of a pilot survey which gave a picture of what access to information for renal patients in Europe to make an informed choice was like at that time in 6 European countries.

A wider European survey focusing on information to patients would update this situation. This survey would raise awareness on lack of information about renal replacement options and reveal whether patient choice is secured. The questionnaire has been structured following the 12 Minimum Requirements for Best Practice in Information.

Thank you for filling-in the questionnaire in the language of your choice on line or printed version to be sent by  post to the Patient Organisation in your country.

To use the Survey Monkey questionnaire please
select your preferred language below:
To download a PDF to distribute hardcopies please
select below:

BULGARIAN

DANSKER

DEUTSCH

EESTI

ENGLISH

LE FRANCAIS

ITALIANO

LIETUVIU

MAGYAR

NEDERLANDS

NORSKE

POLSKI

PORTUGUES

ROMANA

SLOVENSCINA

SUOMI

SVENSKA

 


Survey 2011 Bulgarian

Survey 2011 Danske

Survey 2011 Deutsch

Survey 2011 Eesti

Survey 2011 English

Survey 2011 Francais

Survey 2011 Italiano

Survey 2011 Lietuviu

Survey 2011 Magyar

Survey 2011 Nederlands

Survey 2011 Norske

Survey 2011 Polska

Survey 2011 Portugues

Survey 2011 Romana

Survey 2011 Slovenscina

Survey 2011 Suomi

Survey 2011 Sverige

  Copyright © 2010 European Kidney Patients' Federation (CEAPIR): All rights reserved.