This 6 ½ years (July 2011 – February 2018) in shared supported accommodation, has had a significant impact on the deterioration of my disability. This attains to using the phrase ‘on a dunghill’ as a description of my life in a shared supported facility. This term of expression gives readers an idea of the ugly reality; of the helplessness, immobility, failure to speak and see; and of course the power of irritation towards the delivery of life circumstances pertaining to the disability sector. This bureaucratic mess is subsequent to a lack of true empathy, which may conflict with any budget bottom line, thus enforcing the creation of social dilemmas which then draws attention away from the original problem. This is something that can also be performed by non-government authorities, as is seen in my own circumstance.
My aim in this book is to affirm vital principles that must be better understood and implemented if the National Disability Insurance Scheme (NDIS) is going to be of benefit and fulfill its mandate; so that care doesn't become careless.
I want to encourage people to keep on pushing the case for disability justice! My book is aimed at those providing a service to people with disabilities with high support needs. I want to address all who are involved in disability care; professionals, social workers and especially those managing facilities that look after communities and groups of people.
I am giving myself a wide focus in this book, and my aim is not to win a fight, but to present a case.
Peter Gibilisco writes of his experience living with a disability and fighting for his rights. It is a remarkable insight into the frustrations of dealing with bureaucracies for those with disabilities. Peter describes his experiences and his views on how the lives of those with a disability can be improved by changing processes and removing barriers. Peter is to be congratulated on this very important work.- Professor Martin Delatycki Medical Director, Victorian Clinical Genetics Services Director, Friedreich Ataxia Clinic, Monash Medical Centre Co-Director, Murdoch Children’s Research Institute
I have worked with Dr Peter Gibilisco over a period of about 15 years. Over that time I have watched Peter’s amazing perseverance, admired his intellect and wondered at his ability to dispassionately scrutinise the situation in which he finds himself. In this book you feel his frustration and raw pain as he critically discusses being disenfranchised by the system that is meant to care for our disabled citizens. This book gives an insight into the true grit of the man and his selfless willingness to take up the fight for the benefit of others who find themselves without a voice.
I can commend this book to anyone with an interest in our disability care sector.- Susan Prior. Editor, writer.
Peter’s experience and knowledge provides insight into how people with disabilities are faced with growing struggles, almost on a daily basis. I believe this book is an excellent depiction of the current state of affairs concerning social exclusion in today’s community.
I recommend this book to anyone interested in finding out more about the political and economical landscape of today’s disability sector.- Steffan Irugalbandara Bachelor of Management | Master of Marketing 2015 Graduate of the Year, Deakin University 2016 and 2017 Student Excellence, Monash University
Dr Peter Gibilisco is a social justice activist who speaks from the dual perspective of a successful academic together with the lived experience of a progressive neurological condition which is having an increasingly devastating impact on every aspect of his life. This book will strike a chord with people who have disabilities everywhere especially those with severe physical disabilities living in shared supported accommodation facilities. With great intelligence and integrity it describes the mental torture associated with a disintegration of control and individuality worsened by factors as fundamental as a lack of empathy and continuity in the caring relationship. It gives voice to serious shortcomings in a system that is failing many in the provision of truly individualised care.- Jenny Williams BA BSW MSW Social Worker, Friedreich Ataxia Clinic, Monash Medical Centre
Friedreich’s Ataxia does not affect my intelligence, but many do not believe this. But the reality is highlighted by my academic qualifications, which are a double degree from Monash University, Master of Arts from Monash University and a Doctor of Philosophy from University of Melbourne. My PhD was achieved late into the progression of my disease, when I was 43 years old. For me this was a huge achievement, especially when you consider the systemic beliefs among medical practitioners around Friedreich’s Ataxia. At the time of my diagnosis, medical specialists told my parents that ‘I would not live much beyond the age of thirty’, let alone obtain a PhD! These days, I still perform research with the university as an honorary fellow. I have written and published over 100 articles and currently now authored three books.
However, there are many degrading effects, such as blindness, very poor speech, hearing impairment, poor heart and limited mobility and coordination. But in all spheres of life, I’ve always tried my best; the jury is out, but there is still some chance that my writings may create change.
This book has been achieved with the assistance of two very good friends, Bruce Wearne and Christina Irugalbandara.
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