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Transition

Transition

Transition, in the context of diabetes care, traditionally refers to the “purposeful, planned movement of adolescents and young adults… from child-centred to adult-orientated health care systems.” (Blum et al. 1993).

Transition

Adolescence can be a difficult time for many young people as they learn to manage new-found freedom and autonomy in a confusing world of new experiences. If you add management of a complicated medical condition into this equation, it is easy to see how healthcare can be placed into the “too hard – I’ll do that later” basket.

At around 15 years of age, many paediatric hospitals and healthcare services begin to transition patients across to adult healthcare. For some, this transition is a smooth and seamless transfer from the supported care of their paediatric specialist team and parents/carers, to more self-motivated engagement with independent healthcare providers. For others, the journey is fraught with difficulties and hurdles which can leave the young person thinking “Do they even remember who I am?” or “Do they even care what I think?”

Unfortunately, this type of experience often leads to young people ‘dropping out’ of the healthcare system, leaving them to fend for themselves with their diabetes management and risking long-term irreversible complications.

Youth Transition Survey

Young people with diabetes are being overlooked by the Australian healthcare system with almost half of 18 to 24-year-olds not getting the support they need to begin adult care, a new study shows. The Youth Transition Survey (conducted in 2011) asked young people living with type 1 and type 2 diabetes about their experience in moving from child to adult healthcare. The study found that 71 per cent of the 14 to 17-year-olds surveyed and almost half of the 18 to 24-year-olds had never discussed adult services with their child-focused healthcare team.

Read the full report

Youth Transition Pack

An exciting project funded by the Commonwealth Department of Health and Ageing through an NDSS Strategic Development Grant and administered by Diabetes Australia is helping to tackle this issue once and for all.

The project’s objective is to develop a nationally consistent youth transition pack to be distributed to NDSS registrants aged 12 to 20 years with type 1 and 2 diabetes, assisting them to transfer from paediatric to adult healthcare. By standardising the resources young people receive, it is hoped the frequency of young people ‘dropping out’ of healthcare will decrease and the long-term cost on the health care system will be significantly reduced.

Created in consultation with a Youth Transition Working Party and consumers, the pack draws on existing resources as well as examining research and information into innovative adolescent healthcare strategies. To view the age-appropriate letters sent to parents of young people with diabetes, click here.

In 2014, an evaluation of the birthday card and letter program was conducted to assess its value to parents and young people and to explore how it might be improved.

The full Youth Transition Pack Evaluation report can be accessed here.

Diabetes MILES Youth Survey

The Diabetes MILES Youth report highlights the psychological, wellbeing and quality of life issues facing young Australians with type 1 diabetes and their parents. The survey was conducted in 2014.

The Diabetes MILES Youth project is a part of the Young People with Diabetes National Diabetes Program.

Click here to download the 2015 MILES Youth Report

Moving On Up

The NDSS Young People with Diabetes National Development Program (NDP) has developed a booklet which focuses on the challenges and opportunities that young people face as they become young adults: how they can live well with diabetes through this time and importantly, the responsibilities they have for their own diabetes care and the support they can expect to receive. This resource includes six sections, focused on moving on:

  • to an adult diabetes service
  • to work, university or TAFE
  • to four wheels (driving)
  • out of home
  • with life
  • with a new diabetes care team

Find the booklet here.

myD website

‘myD’ (my diabetes) is a site that has been developed specifically for people aged 16 to 25 years living with diabetes.

The site provides general information on living with diabetes and covers ‘everyday’ topics like school, work, travel, driving and general health. The site also provides information and links to other sites of interest and places to go for more information.

If you would like further information on any of these projects, contact the project coordinator – Jane Cheney at Diabetes Victoria on 03 8648 1830 or via email.

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