People Power
Empowering grassroots Australia
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Coral Rizzalli

 





Joanne Stuart

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We are a political movement of everyday Australians aiming to represent and empower grassroots people and communities in Australian life, including:

  • families (the foundation of society but unrepresented by any broad, mainstream organisation)

  • small businesses and independent owners (the backbone of our economy and employment but ignored by governments)

  • consumers (the least organised and least vocal component of our economy)

  • people with disabilities, chronic and mental illnesses and their families/carers (the most invisible and vulnerable Australians)

  • the aged (the carriers of our accumulated wisdom but regarded as redundant and unproductive in our culture)

  • volunteers in communities (the glue in society but unrepresented in any of our halls of power)

  • individuals and communities who practice self-help (whose voices are rarely heard in public life)

Both Left and Right have ignored everyday people and social relationships in their obsession with the market and the state. Social relationships - not the market or the state - should be the prism through which we assess policy and determine the public good. This is common sense. This is the Australian tradition.

 

Our National Council

Coral Rizzalli OAM QLD 

Coral lives in Ingham in North Queensland and was awarded a Medal of the Order of Australia for her voluntary work in disability, advocating on behalf of her son, John, and others in similar situations. She is a leading consumer advocate for health reform and the introduction of a person-controlled electronic health record.
Fim Jucha  SA

Fim is a volunteer support worker and advocate with families who have a family member with disabilities. She is a longtime advocate and carer for her sister with a disability. She coordinated volunteers for the successful election of the late Paul Collier to the Legislative Council in South Australia in March 2010.

Lorraine Pestell WA

Lorraine is an advocate for children and parents in fractured families, and has a strong interest in ways of using the taxation and benefit system to recognise the value of unpaid work, such as caring for family members or volunteering, to encourage many more people into caring roles and to provide carers with a sustainable lifestyle.

Libby Hartman  VIC

Libby  is mother of 7 year old Anthony who has autism. Her journey of advocating for the rights of her son has exposed her to a minefield of inequality and prejudice within the education system and beyond. She pens a blog  'Life is Wonderful - despite everything' exploring many of the issues of disability, carers and families.
Terry Ryan  NSW

Terry is the father of a son who has an intellectual disability, two daughters and two grand-daughters. He has been President of ACTION for People with Disability, and Chairperson of Manly-Warringah Family and Friends of People with Disability.

Georgina McAuliffe  SA

Georgina is a part-time anaesthetist and full-time parent, carer and educator for a daughter with autism.
 

 
Paul Oglesby  NSW
Paul was diagnosed with multiple schlerosis (MS) 22 years ago. His illness forced his medical retirement from the ABC when he was an executive in ABC TV Program Development. In 1995 he was elected to the North Sydney City Council,  was re-elected twice, and retired from Council in 2008. Paul currently works as a brokerage assistant in a carers program, organising respite care for carers of people with a mental illness.
Pamella Maram  QLD

Pam lives in Maryborough and is a fulltime carer for two teenage sons with disabilities, and mother of two daughters without disabilities.

Kathleen Lemonis  NSW

Kathleen has dedicated the last 10 years to making a difference to families facing challenges with limited supports. She currently works in providing in-home supports for families where children have an at risk factor (harm/abuse/neglect) inclusive of parents with mental health issues or disabilities.

Michiko Parnell  WA

Michiko is a teacher, and parent of three children, one of whom has high level disabilities as a result of cerebral palsy. She has a strong interest in the development of policies that enhance the ability of new mothers to nurture small children instead of having to return prematurely to paid work, and decreasing the gap between early intervention and intervention past the age of five.
 

Jane Bett  QLD

Jane is a counsellor in drug and alcohol dependence and mental health, with personal experience of mental illness.

 
Jessica Revill  NSW

Jessica is a Sydney psychologist with a strong commitment to person-centred reform in education and disability.

David Ayliffe  VIC

David is a writer and former journalist, a parent of four children, and currently works as a fundraiser for an international not-for-profit organisation.

Sherran Mitchell  VIC

Sherran lives in Mytleford in rural Victoria, her son, born in 1979 has Mowat Wilson syndrome. She is a diabetic and brought awareness to the community which helped form a support group. Because of her son, she advocates for people with intellectually disabilities living in SSA homes. She has also advocated for the rights of people in aged care facilities and people with mental health issues.

Deborah Charlton  TAS

Deborah is coordinator of the Family Inclusion Network in Tasmania, and a foster carer of a young boy who has sustained severe trauma. She is passionate about families and children in the child protection process getting a fair go, and is a keen advocate for early intervention to support and empower families in staying together rather than waiting until it is too late and having to remove children from their parents.
 

Leane Leggo  VIC

Leane is a parent of a child with a disability, and president of a communication therapy and support centre in Melbourne for people who cannot speak.
Lori Crompton  NSW

Lori is a program manager in a primary health care organisation, and is passionate about new models of preventative and holistic care.

Mandy Miles  NSW
Mandy has been a carer for the last 15 years, and works as a program manager in mental health. She founded a children's charity (Make a Difference) in 2000, which supports families and children as a charity of last resort.  [photo: Mandy, right]
Vern Hughes  VIC

Vern is a parent of three sons, two with autism. He lives in Melbourne. He is Director of the Centre for Civil Society.
 
Sam Mauchline QLD

Sam lives on the Gold Coast with his wife Anne and has two children, Jill the eldest and Paul who is severely disabled suffering from cerebral palsy. Sam very passionate about achieving immediate changes for those with disabilities, their families and carers.
 

Joanne Stuart  VIC

Joanne Stuart is a parent of a son with autism. She lives in Ivanhoe in Melbourne and has been active in local communities affairs for 25 years. Joanne is completing a law degree, in between battling government departments and service providers in search of better supports for her son with autism.

 

Contact Us

info@civilsociety.org.au

Secretariat:

0425 722 890

info@civilsociety.org.au


PO Box 159
Yarraville Vic 3013