Good afternoon,
Please find enclosed within this email,
responses from the Conwy Social Care Department, in particular from
Managers of the Disabilities and Vulnerable People Services.
- The
general principles of the Autism (Wales) Bill and the extent to
which it will make provision for meeting
the needs of children and adults with Autism Spectrum Disorder
(ASD) in Wales and achieve the aim of protecting and promoting
their rights; The Bill is
not clear on general principles as is for example: the
Additional Learning Needs and Education Tribunal (Wales) Act
(2018), the Social Services and Wellbeing (Wales) Act (2014) and
the Wellbeing of Future Generations (Wales) Act 2015. I would argue
that the principles of the SS& Wellbeing Act (Wales) 2014 are
relevant and are focussed on protecting people’s rights
irrespective of diagnosis. I am aware that the Bill is intended to
complement the ALN, & SS&WB Acts, but it is very much
focussed on provision of services rather than on individual
wellbeing outcomes.
-
Any
potential barriers to the implementation of the provisions and
whether the Bill takes account of them;
Capacity to undertake a proper and holistic diagnosis. Impact of
Brexit on the NHS and ability to respond. Impact on Wales of the
Brexit in terms of support staff. The interface between rights of
the individual set out in this Bill and those enshrined elsewhere
especially within the SS&WB Act.
- Whether
there are any unintended consequences arising from the
Bill; - This would
create a two tier system where the rights of people with Autism to
access diagnosis within a specified period could impact on the
rights of other people with disabilities to have access to
diagnosis.
- Capacity
within Organisations to respond to timescales would drive the focus
of services and delivery. Diagnosis is an output and not an
outcome, this Bill is contrary to the SS&WB Act which is
focussed not on diagnosis but on rights, wellbeing and outcomes. It
is interesting that a focus of the Bill is diagnosis, yet the
Neurodevelopmental Pathway work is very much focussed on
outcomes for the child. We understand that families want a
diagnosis as this enables them to understand their child’s
world better, but there are also often expectations that with a
diagnosis comes access to services. We need to switch the
thinking and culture towards outcomes in line with the SS&WB
Act. This Bill is a retrograde step from the aspirational
SS&WB Act (move from service led to focus on the person). The
memorandum states that it is complementary, but it interferes
with the guiding principles of the SS&WB Act for a specific
group of people.
- Introducing a
42 day timescale for assessment of need may be appropriate for
children and in line with SS&WB Act but is not so for adults
and would result in an inequitable approach. Currently there are
locally agreed PI’s but not national ones on timescale for
assessment. Which would be the primary diagnosis for someone with
and a Learning Disability and ASD?
- We feel
strongly that the Bill, if it is to proceed should not stray
in to areas already covered by the SS&WB Act and ALN Act. That
if it is to proceed; the Bill should only focus on areas that are
not covered by other legislation.
-
The
financial implications of the Bill (as set out in Part 2 of the
Explanatory Memorandum); -
·
The
appropriateness of the powers in the
Bill for Welsh Ministers to make subordinate legislation (as set
out in Chapter 6 of Part 1 of the Explanatory Memorandum).
- The
regulation-making powers in this section allow the Welsh Ministers
to make regulations, which include, for the purposes of this Bill
only, other neurodevelopmental disorders in addition to the WHO
International Classification of Diseases definition of
‘autism spectrum disorder’. – that could include
Learning Disability and a whole other range of Neurodevelopmental
conditions such as dyslexia, dyspraxia, ADHD etc.