Autism Global Network: Autism SA

Showing posts with label Autism SA. Show all posts

Thursday, June 4, 2009

Kristie and her Family at the Autism SA Awards Ceremony

Kristie's family: Shane (Dad), Elaine (Grandma) & Allison (Mum)

Autism SA Awards Ceremony

From left: David Palmer - Autism SA's Number 1 Ambassador; Jessica Bostock - Autism SA's Community Relations Coordinator.
David and Jessica are a couple of wonderful Autism SA staff that made Kristie feel so comfortable to be at the Awards Ceremony. Thank you so much for encouraging and supporting her.

Wednesday, June 3, 2009

Kristie Dressed by Noushke, Adelaide (AutismSA Awards Ceremony)

Kristie was kindly dressed by Deanna Bellini of Noushke (Adelaide, South Australia). Deanna opened her store especially for Kristie and made her feel like the princess that she is. Thanks so much Noushke for making Kristie feel confident in the beautiful clothing she was so lucky to have for the night. xxx (Kristie is picutred here with Deanna and her beau, Zaik)

Kristie Dix, who has Asperger's Syndrome Performs Solo

Although Kristie has Asperger's Syndrome (a social disorder on the autism spectrum), she mustered up all her courage to perform her solo rendition of 'A Thousand Miles' by Vanessa Carlton at the Autism SA's Awards Ceremony held on Wednesday 27th June 2009.

Kristie was really nervous about singing solo in front of a large crowd at an official function for the very first time. The courage it took for her to follow her dreams of becoming a singer and to put all her fears and insecurities aside to make them come true, made this a truly inspirational and heartfelt moment for all who watched her.

To ease her into her rehearsal, she held her Mum's hand for the first practice, let her sit on the edge of the stage for the second, and then allowed her to sit at a table for the third. The video of Kristie on YouTube is her third practice at the rehearsal. http://www.youtube.com/watch?v=hA2VOuaN64g

Letter to the PM 28th July 2009

Dear Prime Minister,

We sincerely thank you for the opportunity to meet with you to discuss what we are doing to enhance the lives of families living with autism in Australia and globally. We congratulate you on your election promise to provide better autism services and on its implementation, while at the same time putting autism on the political agenda.

In March 2009, I founded with my husband’s full support, an organisation called Autism Global Network. The organisation was established in honour of our three beautiful children, Kristie (10), Jacob (5) and Aaron (5), who were all diagnosed as being on the autism spectrum in July 2007.

While Australia’s official prevalence rate for autism is 1 in 160, which only reflects the rate for children aged between 6 and 12, more alarming figures exist globally. A recent Cambridge University study has found that as many as 1 in 64 children could have autism, due to many children going undiagnosed.

Social inclusion for the whole family is the foundation from which we base our work. As a family, we have personally chosen to embrace autism, to have a positive outlook and to focus on what the children can do, rather than their disability. Based on our own personal experience, we have come to learn that the children can’t achieve their full potential unless the whole family’s needs are supported.

Our Mission Statement for Autism Global Network accurately summarises what we strive to achieve for our families.

"Autism Global Network is an innovative and dynamic organisation that provides knowledge, support, care and understanding to people dealing with autism to enable enhanced opportunities for social inclusion and quality of life. With our drive and passion, we strive to advocate for the human rights of our families and promote community awareness and inclusion at every opportunity."

Our greatest personal achievements have been a direct result from a ‘team effort’ that is driven by us. Our support network comprises of us (parents), siblings, support groups, therapists, educators, and medical professionals. This success is almost impossible to achieve because a large percentage of families are already experiencing social exclusion at the time of diagnosis. In addition, many parents, especially the mothers, are suffering from depression due to the extreme behaviours and lifestyle that comes with raising a child on the autism spectrum.

The most significant difference that our Government’s could be making to parent’s very large stressors is to significantly improve the education system for our children with an autism spectrum disorder. The issues here are endless and of which ultimately leads to the children and their families being excluded from society in almost every way. Many children are being forced to be home schooled because they are not eligible for the special school system, mainstream schools can’t cope with their high level needs and there are simply no places available in the limited number of special units.

For our family, schooling is the most significant stressor and will continue to be for many years to come. The State Governments need to do much more to improve the existing education systems and the lives of families living with autism spectrum disorders. Our children deserve the human right to be given a chance of becoming functioning members of society, where they are employable and therefore pay taxes.

The saddest loss a family living with autism can face, besides the 80-90% divorce rate, is the loss of the family home as a direct result from the extreme medical and therapy bills necessary to give the child any chance of an independent life as an adult.Our deep belief is that it is possible families can be empowered to implement basic, but effective therapy principles into their everyday life at a much lower cost than the current system and therapy methods indicate. If we were to hire a therapist to provide our three children with the recommended 20 hours a week therapy each at an average cost of $50 an hour, our gross annual bill would be $156,000. In addition to this are educational expenses, medical professional consultations, therapy equipment and expensive medications.

Attached to this letter is a summary of the services we currently provide to families living with autism and a business model outlining our future plans. We are passionate about helping to improve the lives of families living with autism at a national and global level. We hope to achieve this in a proactive manner by working closely with the Federal Ministers for Education and Social Inclusion; Health; Families and Community Services; to achieve positive and cost effective outcomes. We invite your Ministers to contact us any time.

We also want to bring to your attention the wonderful support we have been given by Tony Zappia, Member for Makin. Tony is the chief patron of our Rainbow Land Play Time family support group where we currently run a playgroup for the whole family on a Saturday. Thank you again for the great honour of meeting with you today and we very much look forward to more meetings in the future.

Yours sincerely,
Allison Dix
Autism Global Network

Representing the Autism Community

Thursday, June 4, 2009

Kristie and her Family at the Autism SA Awards Ceremony

Autism SA Awards Ceremony

Wednesday, June 3, 2009

Kristie Dressed by Noushke, Adelaide (AutismSA Awards Ceremony)

Kristie Dix, who has Asperger's Syndrome Performs Solo

research study about various aspects of parenting a child with an Autism Spectrum Disorder

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Letter to the PM 28th July 2009