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ACQ

Volume 12, Number 3 2010

151

notions of competence (both professionals’ views on

the competence of individuals with aphasia, and the

changing views of people with aphasia with respect to

their own competence). The practical suggestions and

insights provided will challenge clinicians to implement

changes to their own services in order to make them

more accessible.

The second article, “Communication access to

health and social services”, describes a project in which

individuals with aphasia worked together with staff at

Connect to design a training program to enable service

providers, particularly those in health and social services,

to audit and improve communication access to their

services. Individuals with aphasia were involved in all

stages of developing the project, with the project team

including one person with aphasia, as well as the support

of an advisory panel of six people with aphasia.

The simple framework described in the article for

addressing communication access could easily be

adapted for any organisation wanting to improve their

services. The framework describes three phases of

a user involvement with a service: a beginning phase

(e.g. making an appointment), a middle phase (e.g.

the encounter with a service), and an end phase (e.g.

a follow-up from the service, or leaving the service).

At each phase, three components of communication

access can be considered: documents (e.g. appointment

letter, website), interactions (e.g. phone calls, interacting

with a receptionist), and environments (e.g. physical

arrangements in the waiting room). The authors

also suggest that one of the most powerful tools for

educating service providers about the importance of

communication access is the use of real-life stories

(e.g. a video of a person with aphasia describing their

experience in accessing a service). Real-life stories

encourage service providers to put themselves in the role

of service user, and to reflect on the impact of not being

able to access a service because of a communication

disability.

Underlying both of these articles is a strong thread

of user involvement that demonstrates Connect’s

commitment to an inclusive organisational culture and

values. The authors describe how the social model of

disability has influenced their approach to communication

access. A basic tenet of the social model is that “lack of

participation and involvement of people with disabilities

is often more a function of the barriers in society than

it is a result of inabilities on the part of people with

impairments...if people with impairments were given

equal access, they would not be disabled” (Parr, Pound,

& Hewitt, 2006, p. 190). Parallels are drawn between

physical and communicative access, with the authors

arguing that just as a ramp can provide access for

people with motor impairments, communication access

can provide individuals with communication difficulties

the ability to access and engage with organisations

and services. The authors also make the point that

communication access means much more than just

making a few documents accessible. They suggest

that in order to make authentic rather than tokenistic

improvements to communication access, an explicit

focus on organisational values and sustainable whole

systems changes are needed.

While this may make communication access sound

like an impossible hurdle to jump within our already