“…Unfortunately, instead of the internet being a useful tool for providing comprehensive, quality information regarding AIS and treatments, research indicates that the information that is currently on the internet is poor, irrelevant, and misleading (Mathur et al, 2005;Wellburn et al, 2013). For example, studies have found that the information regarding AIS on the internet is not evidenced-based and is inaccurate (Mathur et al, 2005) and lacks information regarding how treatments work, the associated risks and benefits of treatments and how treatment choices can affect qualityof-life (Wellburn et al, 2013). Research indicates that the information acquired online can generate greater confusion and result in unrealistic patient expectations (Ahmad, Hudak, Bercovitz, Hollenberg, & Levinson, 2006).…”