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Person-first language: what are your thoughts?
Within the disabled and chronic illness communities there is a push for the use of person-first language. For instance, rather than referring to someone as disabled, they would be called a person with a disability. In the context of CF, this means nixing phrases like “CFer” and instead, focusing on people for who they are rather than what they have (ie: a person living with CF). Person-first language is generally considered to be the most respectful way to talk about people with disabilities or differences, but I wonder…. how do you feel about it?
Do you want to be called a patient/CFer, or do you prefer the term person with CF?
How important do you think person-first language is?
What terms do you use when referring to yourself? CFer, cyster/fibro, adult with CF, other?
If you are the parent to a child with CF, how do you want others to refer to them?
What are your thoughts on person-first language?
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