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My Daughter is Leaving Home: Reflections on Living Independently


by Charles O'Mahony on September 5, 2011

We are delighted to welcome this guest post from Noelin Fox.  Noelin is a Ph.D candidate in the Centre for Disability Law and Policy, NUI Galway.  Her research examines the right to independent living provided for in Article 19 of the UN Convention on the Rights of with Disabilities.  Noelin has worked for many years in intellectual disability services’ in Ireland.

This month, my daughter, like thousands of her peers across the country, is moving away from home for the first time.  She is 18 years old and is taking up her place in college, embarking on her journey to independence.  Over the coming months she will have to learn a whole array of new skills which she has no previous experience of.  She will have to manage her (limited) budget, feed herself properly, learn to live with people who are not her immediate family, manage the academic work she is assigned, deal with the bank, figure out bus time-tables, forge new friendships and a whole array of other tasks.  In the process she may well make mistakes.  She may submit work late for college, spend too much money on going out leaving herself short at the end of the week, get involved in unwise relationships, among many things.  Hopefully she will learn from such mistakes and manage better the next time.  Throughout this process she will have plenty of support – from us her parents, from the school-friends she is living with and from new friends – and if she gets her heart broken or bruised we will take care of her until she heals and help to her move on.  The college too is well attuned to the needs of in-coming first years – it has good structures in place to ease them into college life and help ensure they progress through their first encounters with third level academic studies.

How different all this would all be if she had a disability, especially if she had an intellectual disability.  Would she be leaving home at all at this stage of her life at all?  Probably not – and there are many reasons why this is so.  On a practical level she may not be allowed to open a bank account or sign a lease for her accommodation.  If she were deemed by a medical doctor to be unable to manage her money, any disability benefits she received would probably be paid directly to us.

And where would she go anyway?  There are so few mainstream third level education options open to people with intellectual disability.  Third level colleges may have disability support services for students, but gaining access to the regular courses is a problem and there are few courses designed to meet the needs of people with intellectual disability in this sector.

On another level we may feel that she would be safer at home, worried that she would not be able to cope with life without our immediate support and guidance – would she be vulnerable to being exploited, would she be able to manage getting the bus, would she get involved in inappropriate relationships, would she manage her course work?  And if she needed support at home where would this come from and how would it be paid for?

Our systems and structures are designed to support my daughter’s progress from home to college and on to employment.  The pathways are clear and open.  It is assumed by her family, her schools and her community that she will learn the skills she needs to progress through the systems and become a fully-fledged independent adult.  These positive assumptions about her abilities are built into and supported by our structures and systems.  For people with intellectual disability the opposite is the case.  Quite apart from the worries of parents’ about the ability of their disabled sons or daughters to manage life independently, the lack of clear pathways is an enormous obstacle.  For young adults with intellectual disabilities the most likely route after school is some form of training or day services provided by a disability service provider and funded by the health services – not education.   Although FAS funds some training programmes for people with disabilities, the vast bulk of day services and training for people with intellectual disability is funded from the health budget.  So, while our educational obligations to most young adults continues into their twenties, it seems to end at eighteen for those with intellectual disability.  This means that if a young adult with intellectual disability does not want to attend a specialist (and in effect a segregated) post-school education or training programme, she will in general have to forge a path largely unassisted by our state systems – which in the main only provides recognized pathways to specialist/segregated services for her.  There are some notable exceptions such as the Certificate course in Contemporary Living offered by TCD and the new ‘Going to College’ pilot scheme starting this Autumn in NUIG.  But the point is that these are the exceptions and third level colleges are only just beginning to develop options for people with intellectual disability.

Article 19 of the UN Convention on the Rights of Persons with Disabilities asserts the equal right of all persons with disabilities to live in the community with choices equal to others, and to be fully included and participate in the community.  People with intellectual disability, just like everyone else, must learn the skills they need to achieve this successfully, and have the opportunity to develop their own relationships with others, independent of family.  This will mean that they, just like everyone else, probably will make mistakes along the way and hopefully they will learn from their mistakes.  Many of us, however, disabled or not, never learn from our mistakes and may in fact end up repeating the same mistakes over and over again – how many people, for example do we know who repeatedly make poor decisions about relationships.  Family or friends may offer advice when this happens, but we do not and cannot stop them, nor should we unless they break the law.  Yet if a person with intellectual disability makes a mistake she probably won’t be allowed to make it again, and indeed it is more likely still that she will never be provided the opportunity to make the mistake in the first place.  This will probably be framed as protecting her, but it has the consequence of stopping her from learning what she needs to learn in order to get on with her life.  How else will she learn if she is protected and segregated from real life in the community?  To become adults in charge of our lives we all need the chance to learn from experience, and to learn the skills we need we all have to given our independence and the chance to live in communities.

Making real the right to independent living and community inclusion means:

1.                  Ensuring that our legislation – and particularly our new legal capacity legislation – makes positive assumptions about people’s abilities and supports people in their decision-making where this is needed.

2.                  Ensuring that our policies, structures and practices are truly open to all citizens, including people with intellectual disability, and that any barriers currently blocking people’s path to independence are eliminated.

3.                  Developing recognized and accessible pathways to independence for people with intellectual disability, which are not separate from those of their peers.

4.                  Using our resources to support people in living their lives as part of the community so that they too can make their way in life as they see fit.

A sea-change in attitude is needed , away from paternalism and protection – which has served people badly – to inclusiveness and expectation.  We always assumed that our daughter would leave home for college.  For her, this time of her life is full of excitement, challenge and expectation.  For us, of course, it is a little sad and not a little costly!  But we are delighted for her and would never attempt to stop her going.  It should not be so different for the many young adults with intellectual disability at the same stage as her, and their parents.  There is a great injustice in this and it is something we can change – it is not so difficult but it does require some determination to change on all our parts.


07.10.2011

All news:

Celebrating the 3rd December 2007
FILM FESTIVAL OBSERVING 3 DECEMBER
National Umbrella Organisation mark 3rd of December
ENDING OF SHARE SEE TRAINING PROGRAM
SHARE SEE IV MODULE – NISKA BANJA
IMPORTANT DAYS TO CELEBRATE
To Ministry of Labor and Social Policy
SHARE SEE training in Predejane
Recognising the Rights of Girls and Women with Disabilities
SHARE SEE IV MODULE IN SMEDEREVO
Creation the Local Plans of Actions in Disability Area
SHARE SEE IV MODULE – BELGRADE
TODAY IS THE DAY OF UN
Goodbye mouse hello voice controls
Elena Pecaric
Award
AWARENESS RISING
INTERNATIONAL DAY OF POVERTY REDUCTION
ADA RESTORATION ACTION CENTER
WHERE IS SERBIA
Disability Rights Treaty on Verge of Making History?
The Days of European Heritage in Belgrade, 20-30 of September
Council of Europe in Zagreb
Seoul Declaration
Virtual interpreter turns speech into sign language
Strasbourg Freedom Drive
UN Convention
Jagodina hosted the Third Table tennis tournament "Jagodina Trophy"
Hungary ratified UN Convention
Convention on Child Protection
UN convention on disability rights reaches milestone in signatories
IIIrd INTERNATIONAL SMILING CHILD FESTIVAL
Your dressing room on the Internet
Chosen home life a basic right for disabled people
SPORT RESULTS
What Can They Do?
III Module of trainings accomplished
SHARE SEE trainings
Project with young activists finished
Special EUROBAROMETER 263 “Discrimination in the European Union”
Seminar on Independent Living in Macedonia
It's Deaf Awareness Week 7-13 May
International Day of Families (15 May)
European Coalitions
Social services in South East Europe
Test on Autism
UN Headquarters, New York, NY
Presentation the UN Convention in Belgrade
Presentation of UN Convention on rights of persons with disabilities in Jagodina
SHARE SEE training in Belgrade
SHARE SEE training for Leskovac cluster
SHARE SEE Module II in Nis
The U.S. Embassy has a pleasure to invite you
SHARE SEE trainings Module II
I N T E R V I E W
GATEWAY
DYSGRAPHIA
UN Study of Violence Against Women Finds 50% of Disabled Women Experience Abuse
Launch of the Year of Equal Opportunities
Interesting events
Survey reveals social attitudes to disability
Homes that Meet Life’s Changing Needs
Awards for the best Campaign, PAs and users within the PASS project
Design for Everyone, Disabled or Not
STRATEGY
EDUCATION FOR MEMBERS OF POLITICAL PARTIES IN NOVI SAD ON BASIC FACTS ON DISABILITY ISSUES!
AWARDS COMPETITION
UN Convention adopted
Tribune on UN Convention in Novi Sad
Round table in Sarajevo
Evropean Union and Persons with Disabilities
Promotion of International Convention on Rights of Persons with Disabilities
PASS presentation in Bosnia and Herzegovina
International Day of Disabled Persons
World Congress on Disability
N. Korea puts disabled in camps
Universal Design
European Conference in St Petersburg
UN reward to Poland
SHARE SEE Training in Belgrade
Antidiscriminatory practice in Norway
SHARE SEE Training in Leskovac
UN Convention
DISABLED PEOPLE FROM SPANISH INDEPENDENT LIVING MOVEMENT HAVE CANCELLED THEIR LOCK IN
8th Session of the Ad Hoc Committee on the Rights and Dignity of Persons
UN AGREES ON DISABILITY TREATY TEXT
Geneva, 23 August 2006
SHARE SEE Training in Smederevo
SHARE SEE Training in Krusevac
UN Convention - 13 August 2006
Independent living hope
8th Conference of the European Union of Supported Employment
The implementation of Poverty Reduction Strategy goes on
Independent Living seminar in Tirana
E-ACCESSIBILITY TO BE THEME FOR INTERNATIONAL DAY
New CIL branch
CIL Sport Competition
United Nations takes a big step towards accessibility
Social service for PWDs in the Republic of Serbia
New EU diversity spot airing on MTV
Study visits in Brussels for delegates of disabled people organisations from the Western Balkans on 27-29 June 2006
Poverty
EDF Annual General Meeting
Brochure on CIL 10th Anniversary



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