Good Practice in Action 063
Good Practice in Action 063
Copyright information
Updated Good Practice in Action 063 Clinical Reflections for Practice: Equality,
diversity and inclusion (EDI) within the counselling professions is published by the
British Association for Counselling and Psychotherapy, BACP House, 15 St John’s
Business Park, Lutterworth, Leicestershire, LE17 4HB.
t: 01455 883300 f: 01455 550243 e: [email protected] w: www.bacp.co.uk
Context
Purpose
Using Clinical Reflections for Practice resources
1 Introduction
2 Therapeutic setting for vignettes
2.1 Referrals and service remit
3 Case studies
3.1 Vignette 1 – Bert
3.2 Vignette 2 – Lilly
3.3 Vignette 3 – Rani
3.4 Vignette 4 – Tanith
3.5 Questions for reflection
4 Observations for practice
4.1 Equality, diversity and inclusion (EDI)
4.2 Ethical Framework
Conclusion
About the author
Further resources
Purpose
In this resource, the terms ‘practitioner’ and ‘counselling related services’ are used
generically in a wider sense, to include the practice of counselling, psychotherapy,
coaching and pastoral care. The terms ‘therapist’ or ‘counsellor’ are used to refer to
those trained specifically as psychotherapists and counsellors.
It may appear a simple task to define how equality, diversity and inclusion (EDI)
are encountered in practice, but EDI bring an expectation for us to not only be
mindful of the overall concepts, but also to develop a holistic view of the person we
are working with and the unique relationship which is being formed. If we as
practitioners want to avoid the risk that some aspects of our clients may go
unseen, we need to look beyond appearance and physical capacity, beyond
gender and cultural backgrounds as the concept of EDI genuinely encompasses all
our lives. For example, think back over your life, have you ever felt unseen by the
world around you? Or that you were being treated differently to others? Or blocked
from doing something you really wanted to do? While these are often normal
experiences of living they can also be the m. anifestation of discrimination and
exclusion.
In light of the Equality Act’s differing application across the UK, the following
vignette’s focus on two overarching themes: the protected characteristics, and our
obligation to make reasonable adjustment and what this may look like within
therapeutic relationships. This resource does not provide specific guidance, rather
its aim is to increase our awareness of how EDI can be present in practice. To this
end, these vignettes feature fictional composite characters drawn from the
experiences of a range of BACP members working in settings from private practice
to the NHS and voluntary organisations. They are all written from the client
perspective. All the therapeutic sessions take place in a fictional counselling
service and should not be perceived as the only way in which EDI may be
encountered in practice. Following the vignettes there are some questions which
you may wish to consider, together with some general observations which are
included at the end of the resource to support further reflection. Other resources in
respect of EDI include: Good Practice in Action 062 Commonly Asked Questions
about EDI, and 108 Legal Resource EDI.
The concept of EDI has been entwined within a changing society for decades, with
the pace of change slowly building as the structures needed to support an inclusive
society evolved and discrimination began to be challenged.
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Psychotherapy
While steps were taken to tackle discrimination in some specific contexts, it was
not until the Equality Act of 2010 was passed that a unifying piece of legislation
was instigated.
The Equality Act introduced a working definition of EDI with the aim of enhancing
inclusion within society through the identification of different specific characteristics
where discrimination could be experienced within society. These protected
characteristics of age, disability, gender reassignment, marriage and civil
partnership, pregnancy and maternity, race, religion and belief, sex and sexual
orientation are at its core and provide a clear scope of its application.
The other key responsibility, which the Equality Act introduced was the obligation
to make reasonable adjustment to ensure accessibility for disabled people. In this
case the decision of what comprises a reasonable adjustment is not specified by
the legislation or determined by either party but is subject to negotiation if legal
precedent does not exist.
While these overarching themes cover the whole of the UK its application can vary
in England, Scotland, Northern Ireland and Wales and local guidance should be
sought where necessary.
Fictional Charlotte House was built in the early 1920s as a care home for wounded
servicemen, surrounded by gardens and allotments to feed the home’s residents.
Since World War II, the outdoor space has gradually been reduced, being re-
developed to provide much needed local housing and only a small paved seating
area and six staff parking spaces remain. In the mid-1960s the building was
transferred to the NHS and had a variety of uses before becoming the local base
for mental health services in 1973.
In the years following the millennium, the local Clinical Commissioning Group has
implemented a rolling review of its service provision, and it was decided that it
would be more appropriate for mental health services to be contracted out to an
independent provider. As the staff were keen for the service to be retained, ABT
Community Engagement was created and secured the contract in 2005 at which
point management of the services 60 volunteers was transferred to ABT.
ABT became a social enterprise the following year and raised the funding it needed
to complete essential maintenance and modernisation works to ensure Charlotte
House would meet the needs of all service users and it now has two distinctly
separate spaces. The ground floor being the community space including a café,
large rooms for clubs and groups to meet in, along with the office space for ABT,
main reception, two rooms used by the Community Mental Health Team for mental
health assessments and ABT’s drop-in advocacy service along with stairs to the
first floor.
The first floor comprises the protected counselling space with four one-to-one
rooms, two couple’s rooms and a family room along with the private waiting area.
From the outset ABT’s fundamental goal was to make free counselling services as
accessible as possible providing open-ended interventions for adults. Sessions
could take place between 9am and 9pm Monday to Friday, 9am to 5pm on
Saturdays and Sundays, by appointment.
The service has also responded to requests from its counsellors and now makes
the counselling rooms available for rental on an hourly basis by private
practitioners in the evenings and weekends. In order to make the separation
between private and ABT clients clearer, a separate entrance has been created
providing direct access to the counselling rooms for private clients.
The following series of fictional vignettes are intended to enable you to reflect on
how issues relating to EDI may present themselves in practice. As you read
through them, be mindful of the protected characteristics and the potential need to
make changes in how services are provided for the person. After you have read
the last vignette about Tanith, there are questions for you to think about (and for
discussion) in respect of all the vignettes.
The assessment was comparatively brief, confirming the above information, the
primary presenting conditions being sadness and loneliness, that he had no
specific access needs and that he had been made aware of the terms and
conditions relating to the service’s scope.
You have been working with Bert for three months and his attendance has
generally been good, but the reduction in the family income following his wife’s
death now means that he no longer drives and is dependent on public transport, or
community transport services, which he finds demeaning. In his early sessions he
was often angry in the room with you, focusing his aggression on the unfairness of
his life. Over time though he has begun to trust you, becoming slowly more candid
and you have formed an effective working relationship with him.
In recent sessions Bert has been talking about how he now just feels lonely and
unhappy all the time and has picked up a couple of the leaflets for the groups
which meet on the ground floor; while accepting the possible benefit they could
bring he isn’t really sure whether he would want to be that involved as, ‘that was
Dot’s job’. He is also concerned about what people might think when it gets out that
he is coming to see you. Running in parallel with his loneliness, he has also
recently been acknowledging the benefit which talking to you is having for him but
he is starting to become anxious as to what will happen when his sessions run out.
At present, she still lives at home with her mother, her father dying before her first
birthday and she has no memories of him. She was born deaf blind as her birth
was extremely premature due to her mother’s severe pre-eclampsia. Her mother
has empowered her by making sure that all her close family learned to hands-on
sign to ensure her home life was as inclusive as possible. Sadly, her mother is now
developing dementia and as it is no longer felt safe for them to keep living together,
Lilly has decided its time to move out to supported housing but she is increasingly
anxious over the practical challenges this will present.
Despite her fears over what the future holds, Lilly sees the real benefit of
counselling and wants to come as she knows her life is changing forever. As this
was her initial assessment session, she brought her younger brother, Danny, to
‘hands on’ sign for her, but feels it would be inappropriate for her siblings to attend
her sessions.
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Psychotherapy
From the outset it was apparent that this style of communication would take longer
than usual and two further appointments were needed to complete her
assessment. Lilly was adamant that she doesn’t want to have any existing
connection with the translator and as the deaf blind community is comparatively
small it took two months to find somebody she felt able to work with.
The signer was articulate and engaging, but ‘hands on’ signing proved very time
consuming and tiring, sessions being broken into two 20 to 25-minute slots with a
short break in the middle. Lilly finds the interruptions irritating but her commitment
remains undimmed as she has begun to explore parts of her life she has always
felt unable to look at. Whilst progress is slow, Lilly begins to risk considering how
she sees herself, and the experience of being loved, but she also acknowledges
her fears that with only three sessions left, and without the financial resources to
pay for more sessions, she will not have enough time to think about it properly.
The GP’s covering letter confirmed that the referral was being made following a
discussion with her oldest son Belwinder, a doctor working in orthopaedics. Since
the baby’s death, he was aware that his mother had become less active and was
reluctant to engage with her family. In her assessment, it was noted that while she
easily communicated with the assessor, her son had also attended, often
interrupting to correct her response if he saw things differently; Rani always
deferred to his perspective.
While a family member would bring her to ABT for her sessions and take her home
afterwards, they always waited in reception. Rani focused in her early sessions on
the losses in her life starting with her parents’ deaths in India over 40 years ago;
whose funerals she was unable to attend, two miscarriages and her husband who
she described as being her support and protector.
GPiA 063 Copyright © 2016–2019 British Association for Counselling and
Psychotherapy
Rani is engaging in her sessions, welcoming any observations you make,
acknowledging them as being ‘so powerful in helping her understand and start
trying to change’; at the end of her fifth session you note that she has always
deferred to your perspective. As Rani’s sessions progress, she often ends her
sessions by commenting on how much better she feels from seeing you.
Unusually, Rani’s session was cancelled today but the clinical lead at ABT checks
in with you as Belwinder had called to express his, and his siblings concerns, that
despite seeing you for 12 sessions, their mother remains as detached as she was
prior to starting counselling.
Tanith carefully planned her lengthy journey to ABT for her assessment, but it was
less time consuming than she had anticipated and she arrived 30 minutes early.
While waiting in reception she became visibly uncertain and uneasy as it was busy
with excited people attending a community event and she struggled to access any
of the information displayed. Her assessment notes confirmed that throughout her
assessment Tanith was disconnected responding primarily mono-syllabically and
refusing to sign the contract provided saying ‘I can’t read that, don’t you know I’m
dyslexic?’ before threatening to leave; her referral had only described her as
having a learning difficulty.
Tanith cancelled her first session when she arrived and learnt that a contract,
which she could read, still hadn’t been provided and that no one was available to
work through it with her.
During her first few sessions Tanith swayed from mono-syllabic responses,
avoiding eye contact and fidgeting, often crossing and uncrossing her arms and
legs, to a more relaxed posture with a continual, uninterrupted narrative being
recounted about all aspects of her life. She often appeared oblivious to your
presence. As she spoke Tanith often misinterpreted your observations and
interventions, necessitating clarification and re-phrasing a number of times to make
sure that the language meant the same to both of you. As her sessions
progressed, a reasonable working relationship started to form, and she began to
become more candid over some of the experiences of her life.
Across Bert, Lilly and Tanith’s vignettes, there are differing levels of willingness to
acknowledge the need to request adjustment to improve service access. Lilly and
Tanith are both able to articulate what was needed in order for them to engage with
counselling, but Bert remains reluctant to acknowledge his challenges and
consider whether things can be improved; in this case a counsellor might need to
give some thought as to how to explore what changes may be appropriate with
him.
In all these cases, the need to actively consider the totality of the client, and a
willingness to address possible changes to enhance the effectiveness of the
intervention, are essential in order to provide genuinely inclusive services.
a) endeavour to demonstrate equality, value diversity and ensure inclusion for all
clients
b) avoid unfairly discriminating against clients or colleagues
c) accept we are all vulnerable to prejudice and recognise the importance of self-
inquiry, personal feedback and professional development
d) work with issues of identity in open-minded ways that respect the client’s
autonomy and be sensitive to whether this is viewed as individual or relational
autonomy
e) challenge assumptions that any sexual orientation or gender identity is
inherently preferable to any other and will not attempt to bring about a change
of sexual orientation or gender identity or seek to suppress an individual’s
expression of sexual orientation or gender identity
f) make adjustments to overcome barriers to accessibility, so far as is
reasonably possible, for clients of any ability wishing to engage with a service
g) recognise when our knowledge of key aspects of our client’s background,
identity or lifestyle is inadequate and take steps to inform ourselves from other
sources where available and appropriate, rather than expecting the client to
teach us
h) are open-minded with clients who appear similar to ourselves or possess
familiar characteristics so that we do not suppress or neglect what is
distinctive in their lives. (Good Practice, point 22a-h).
…take the law concerning equality, diversity and inclusion into careful
consideration and strive for a higher standard than the legal minimum.
(Good Practice, point 23).
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Psychotherapy
And that:
This brings clear parameters to practice which all members need to be mindful of.
Some of these commitments have a clear resonance within the vignettes, such as
Lilly and Tanith’s need for adjustments to be made in order to make the service
accessible. However, is there a need for greater understanding of the possible
cultural foundation of Rani’s familial dynamics and should Bert’s increasing
struggles to move around the building be allowed to remain unaddressed?
Conclusion
These vignettes have been produced to illustrate how EDI can be evident in our
relationships with clients but they are by no means an exhaustive list. In order for
genuinely inclusive and accessible services to be provided, members all need to
ensure that they retain a willingness to make adjustments to how they work, where
necessary and reasonable, in whatever setting they are working. More importantly,
however, is that we consider our clients holistically and retain the integrity to raise
issues that we feel may be impacting on our interaction with them.
Further BACP Good Practice in Action resources are listed below along with other
organisations who can provide advice on the interpretation and application of the
Equality Act, which inform the need for an holistic view of our clients, whilst
acknowledging our individuality as practitioners. This should not be taken as an
inference that reading and development opportunities do not exist, rather that their
selection needs to be driven by the people we are and our experiences in practice.
For information and confidential advice on the application of the Equality Act on an
individual level: