“…A small qualitative literature has explored the subjective experience of BPD (Fallon, 2003;Horn et al, 2007;Miller, 1994;Nehls, 1999;Ramon et al, 2001;Rogers and Dunne, 2011;Stalker et al, 2005), most of which has paid some attention, at least, to stigma or discrimination, although these concepts are rarely defined, not the focus of inquiry, and never critiqued or reviewed in the light of the study's empirical evidence. Themes from this literature on BPD and the stigma experienced or anticipated by people with the diagnosis can be divided into two broad categories: the stigma surrounding the act of diagnosis and the label itself (Horn et al, 2007;Nehls, 1999;Ramon et al, 2001;Stalker et al, 2005) and the stigma experienced and anticipated in the context of healthcare (Stalker et al, 2005) including being stereotyped (Haigh, 2002;Nehls, 1999), being subjected to psychological abuse (Castillo, 2003;Haigh, 2002) and having the diagnosis withheld (Castillo, 2003;Crawford et al, 2007;Fallon, 2003;Haigh, 2002;Horn et al, 2007;Rogers and Dunne, 2011) which is linked to being excluded from treatment (Horn et al, 2007;Nehls,1999;Ramon et al, 2001;Stalker et al, 2005) and explicitly contradicts professional guidance (NICE, 2009;NIMH, 2003).…”