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Social visibility of young adults living with Crohn's disease

This short survey is part of a research project for my master's degree at the Université libre de Bruxelles (ULB).

The purpose of this study is to explore how young adults (18-25 years) living with Crohn's disease perceive their social visibility and recognition in the United Kingdom.

Your participation is entirely voluntary, and all data collected in this survey are anonymous: no personal information will be collected.

The data will be used exclusively for my master's thesis and will be stored securely on the ULB servers, in accordance with the university's data protection guidelines.

The data will be permanently deleted once the thesis is completed and evaluated.

By completing the questionnaire, you confirm that:

you are between 18 and 25 years old,
you have been diagnosed with Crohn's disease,
you agree to participate voluntarily.

There are 14 questions in this survey.

This survey is anonymous.

The record of your survey responses does not contain any identifying information about you, unless a specific survey question explicitly asked for it.

If you used an identifying access code to access this survey, please rest assured that this code will not be stored together with your responses. It is managed in a separate database and will only be updated to indicate whether you did (or did not) complete this survey. There is no way of matching identification access codes with survey responses.