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Lost in Transition

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Supporting young people from

minority communities

Bridget Fisher

Head of BME Services ARC



Transition and Best Practice

Hallam University

29.01.10 0

Lots of Hope for the Future









1

Outline

 It is difficult to plan services and improve outcomes if it is

not known who for and how many



 7.9% of the population in 2001 classified themselves as

belonging to a BME community.

 However there is a statistical skew which means a

higher proportion of young people are from minority

communities

 The prevalence of LD in people aged between 5 and 34

is 3 times higher in the South Asian communities







2

“Those who have Mixed heritage have the

youngest age structure where 50% are under the

age of 16. The Bangladeshi, Other Black and

Pakistani groups also had young age structures:

38% of both the Bangladeshi and Other Black

groups were aged under 16, and 35% of

Pakistanis also fell into this age group.

This was almost double the proportion of the

White British group where one in five (20%) were

under the age of 16.”



www.statistics.gov.uk





3

Every Child Matters

The Government's aim is for every child, whatever

their background or their circumstances, to have

the support they need to:

 be healthy

 stay safe

 enjoy and achieve

 make a positive contribution

 achieve economic well-being.





4

Facts and Figures

 In England there are an estimated 12.3

million children aged 0 – 19.

 It is estimated that 2.8% of children have a

learning disability.

 There are 346,000 children aged 0 – 19

with a learning disability.

(Mencap July 2008)









5

Facts and Figures

 There are 85,000 children aged 15 – 19 with a

learning disability. (Mencap 2008)

 From 2009 20% of new entrants with learning

disabilities to adult social care will be from ethnic

minority communities. (Emerson & Hatton LDC 2008)

 This gives an estimated 17,000 young people

from minority communities in transition to adult

services.





6

Only 42% of the senior managers in children’s services and

education were able to provide details of young people’s

ethnicity in out of area placements.

The needs of young people and their families from ethnic

communities were less well addressed in protocols,

commissioning documents and during the interviews. Councils

covering diverse populations told us that their ‘practice was

ingrained’ in meeting the needs of all communities. Overall,

however, there was little evidence that councils had given

diversity issues sufficient attention.



(Growing Up Matters: Better transition planning for young

people with complex needs, Commission for Social Care

Inspection, January 2007)







7

In the second national survey of

Partnership Boards undertaken by the

University of Lancaster, of the 54%

that responded only 22% said that a

race impact assessment had been

undertaken Š either for the board itself

or as part of a wider Equalities Impact

Assessment; and 48% said that no

checks were being done to make sure

services treated everyone equally

whatever communit y they belonged to.

(Hatton, 2007

Young People









9

Young People

Culture is a key part of young people’s identity:

‘The majority of young people identified

themselves primarily according to their cultural

identity and not according to the fact that they had

a disability or learning difficulty. Many strongly

resisted any suggestion that they had a disability

or learning difficulty. This contrasts with the way

staff in services view them.’



(Aasha: working with young people with a learning

difficulty from a South Asian background, 2003)Y



10

‘Generally…impairment is only one part of a

young person’s identity. Other social factors,

including culture and religion, being male or

female and the experience of racial

discrimination influenced how they

experienced disability and impairment.’



(South Asian disabled young people and

their families, Social Care: Race and

Ethnicity Series, 2002)



11

On the whole children and young people

were clear about what they wanted to do;

their parents were less certain what options

would be available and how it would work in

practice. Some honesty and sensitivity is

needed as children and young people

become aware of the reality of their own

disabilities.

(My School, My Family, My Life: Telling it

like it is, DRC, 2006)



12

 Adolescents and adults with a learning disability

from South Asian communities reported that

“double discrimination” led to a lack of culturally

appropriate services, limited friendships and a

lack of leisure activities (Azmi 97).

 Many of the young people were socially isolated

and many had negative experiences at school.

(Aawaaz project, Mencap 2007)









13

 Therefore we are looking at supporting an

increasing number of young people,

educated here, who are possibly in the

difficult position of having all the issues of

moving into adult life combined with

professionals’ expectations of adulthood

and their own family expectations.









14

Families









15

 Some families may never have had

learning disability explained to them.

 They may be hoping for a cure.

 They cannot therefore adequately plan a

future for their disabled child.

 Their aspirations may not be appropriate

for their child.







16

Families are often unaware of the route

of transition. They frequently do not

know about transition planning,

connexions services, or specialist

services.

The transition process seems to have

passed them by.









17

‘While transition plans for children with disabilities

aged 14 and over are a current policy, no parent in

our study reported being aware of a transition plan

for their teenager. However, transition plans are

urgently required, as parents reported great

uncertainty and anxiety about services for their

child after education stopped. Greater consistency

between child and adult services is also required,

as some parents reported that adult services that

had been offered to them did not meet the

language, cultural or religious needs of their child.’

(From Supporting South Asian Families with a

Child with Severe Disabilities, Hatton et al, JKP,

2004)

18

In addition, findings from the Aasha action

research project indicates the extent to which

some families from BME communities are

disenfranchised by financial difficulty and limited

access to English language:



‘There are high levels of poverty in this group.

Many of the parents speak little English and have

difficulty accessing the support that is available

because they do not understand social services

bureaucratic procedures.’

(http://www.skill.org.uk/)





19

 Families/carers from minority communities are

frequently very concerned about the safety of

their young person with a learning difficulty and

can view drives towards independence as

actually neglect.

 A lack of enthusiasm from a South Asian parent

towards greater independence for their child

does not automatically indicate a failure of the

parent to want best outcomes for their child.

Their understanding of ‘best outcomes’ may

differ from that of professionals.





20

Research findings show that professionals need to

make themselves aware of the different range of

attitudes that may be held by parents and carers

who are thinking within their personal value system

and the culture of the community to which they

belong.









21

 There is little evidence to suggest that

informal networks were available to meet

the considerable support needs of

families.

 In a survey of Asian family carers, when

asked to whom they would turn in a crisis

21% of carers did not know of anyone.







22

Talking about the future









23

‘A student had a transition meeting in Birmingham

which was held in the family’s community

language then translated into English for the

English speaking support workers. This was

possible because a facilitator who spoke the

family’s language was used.’

Every meeting should be geared to the young

person’s background and their individual cultural

needs are identified.









24

Bradford Project

“…families who had received support from

the liaison worker felt better-equipped to

help their son or daughter, whereas those

who did not receive help reported continuing

difficulties in gaining necessary access to

services, help and support”

“Making Us Count” FPLD 2005





25

 So a key issue for workers supporting young

people at transition is to help them make the

decisions that are right for them in their own

cultural context.

 To this end the information and support offered

to them as individuals should be fully explained

to their families.

 Much evidence points to the need for families

supporting young people to have a link worker at

transition who understands the culture and the

various different pulls that the young person may

be experiencing.

26

Resources to Help









27

Valuing People Now is based on the recognition of

the human rights of people with learning

disabilities.

It emphasises their rights as citizens:

 To be socially included

 To have choice in their daily lives

 To have opportunities to achieve independence.









28

 There are currently many initiatives

looking at ways of improving services for

people from minority communities. The

National Advisory Group on LD and

Ethnicity meets 8 times a year to discuss

policy/strategy plans and comment on

them.







29

Transition Information Network

 The Transition Information Network (TIN) is an

alliance of organisations and individuals who

come together with a common aim: to improve

the experience of disabled young people’s

transition to adulthood. TIN is a source of

information and good practice for disabled

young people, families and professionals. The

information is provided through a website,

magazine, e-newsletters and seminars.





30

TIN Provides:

 A first point of contact for anyone needing information

about the transition process. Many pieces of legislation

and guidance cover the transition process. They are

from areas including: education, social care, health,

transport, leisure and employment.

 A focus for people accessing information about

legislation and guidance

 A focus for accessing information on good practice so

others can use it. Articles, research reports, guides and

protocols about transition are produced regularly. TIN

records these resources, keeps them up-to-date and

provides information on them for others to access.

 A website www.transitioninfonetwork.org.uk, a magazine

“My Future Choices” and an e-newsletter “Getting a Life”



31

National Transition Support Team

 The programme is running from 2008 to 2011 with a

budget of £19 million.

 The aim is that by 2011 all areas will have a transition

process in place which meets minimum standards and

with many areas achieving good practice in transition

support; and to be able to demonstrate higher level of

user satisfaction. (E.g. disabled children’s services

indicator NI54)









32

National Transition Support Team

The National Transition Support Team has three main roles:

 Drive and shape the programme in local areas through work

with regional advisers, and disabled young people and their

families;

 Engage with and exchange good practice in transition

through websites, targeted information sheets and other

resources to help build capacity; and

 Identify the support needs of local areas and work in

partnership with regional advisers, the Department for

Children, Schools and Families and the Department of Health

to improve transition practice.



33

National Transition Support Team

Year 2

 24 local areas received an extra direct grant of £37,500

to develop best practice and improve support across

transition in other areas (Oldham).

 The 24 local areas who receive direct grants will work

directly with the national transition support team to

further develop effective practice.

 All other local areas will be offered a range of support

and will be contacted by National Strategies and CHaMP

to look at what will be most helpful to each local area.



34

ARC

Member led organisation (mainly voluntary orgs)

Offers members a voice and representation at a

national level

News and policy updates

Various training LDQ - NVQ etc

CRB/POVA

Undertakes a wide range of projects of interest to

Members

BME Services Unit promoting good practice with

ethnic minority communities.

35

Moving On Up

 We have a website www.movingonup.info for young

people at transition. It is a multicultural site.

 An emailed newsletter for professionals Moving On

Update.

 A guidance booklet based on the website has been

produced for families.

 A guidance booklet on key cultural issues for

professionals has been produced.

 We have held fundays for young people in Tower

Hamlets, Bradford, Oldham, Leicester, Luton, Leeds,

Durham and Birmingham

36

Making Things Better









37

 Young people from BME communities face

more difficulties than most:

 Poorly prepared

 Different demands/expectations of them

 Lack of good support for their families

 May not be supported/encouraged into

independency e.g. work or independent living.

 Want to have the same things as other young

people – security a place in society and a

chance to find their dreams.





38

NTST Guide and Framework

 With funding from the ntst, Arc has produced a

Framework document with straight forward tips on

improving transition to adulthood services for young

people from BME communities.

 It has also produced a Guide called “A Guide to

improving Services for Young People from Black and

Ethnic Minority Communities at Transition to Adult Life”

which gives more in depth explanations on why and how

to improve practice.

 These are being launched at an event on January 29th

at Hallam University ,Sheffield.

39

Giving us a Voice



This project started November 2009 and is funded for

18 months by the Department For Communities and

Local Government under its Tackling Race

Inequalities Fund. The competition for this was

extremely fierce. This is the first project to be done

jointly by ARC, BILD and Mencap.

Each organisation is appointing two project workers to

work across the regions



40

is

Giving us a VoiceÕ an 18 month

project working right across the

country to involve people with a

learnin g disabilit y, their families and

carers, from minority ethnic

communities, in regional meetings to

inform local policy makers about what

they need and expect from services

Good Practice in Summary

 Review numbers and start planning now

 Liaise and build relationships with families over a long

period of time

 Use link workers and facilitators as much as possible

 Make sure all staff (including interpreters) are trained in

both cultural and learning disability issues

 Person Centred Planning at transition is meaningful

 Make all records and plans clear and understandable to

all involved

 Research and use the resources currently available and

keep up-to-date with developments

 Set out the procedures clearly



42

Contact Details



Telephone: 01246-555043

Email: bridget.fisher@arcuk.org.uk









43

Thank you









44



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