Address details


Down Syndrome NSW
Level 6/410 Church St, North Parramatta
9am-5pm Monday - Thursday
T: 9841 444


Wednesday, 30 June 2010

Down Syndrome NSW and ACT DSA co-host information events 30 -31 July 2010

for families and for professionals.

Enquiries: Siena O’Brien, phone: 9841 4411 or email: workshops@dsansw.org.au

Both events will be held at

Canberra Southern Cross Club,
Corner Catchpole & Bowman Streets,
Macquarie, ACT


Friday 30th July  
Playing to Their Strengths - a workshop for teachers

$99 per person (DS NSW and ACT DSA members); $132 per person (Non members) 
incl morning tea, lunch and GST
 
Saturday 31st July
Preparing for School - a workshop for parents whose children with Down syndrome are enrolling in Kindergarten in 2011 or 2012

There is no charge for this event.

Flyers and registration forms are also linked from the DS NSW website, under the What’s On? menu, or contact the DS NSW office to have a print copy mailed out.

Tuesday, 29 June 2010

It's that time of year again .....

Please click here to make a donation to Down Syndrome NSW before 1st July, to help support people with Down syndrome and help us realise our plans for the new financial year.
You can also safely renew or apply for Membership and make a tax deductible donation to Down Syndrome NSW online.
Click here to renew your membership to Down Syndrome NSW and make a donation today. You will receive an automatic email receipt to assist you to claim your donation in your upcoming tax return.

Many thanks!

Consultations and Inquiries

A number of State and Federal government bodies are currently conducting inquiries and consultations related to people with disabilities and their families, and some are in the reporting phase.

A new link at the top of this blog,  Consultations and Inquiries provides a list that will help to keep track of them, and the dates submissions and reports are due. The page will remain at the top of the blog.

"Supported living - Creating a home of one's own with self directed support": In Control Australia forum

Monday August 9 2010

Theaterette, NSW Parliament House, Macquarie St,  Sydney

This seminar will showcase Homes West, Brisbane and My Place, Perth, two services that support people with disability in homes of their own with a combination of formal and informal support.

Access a flier and online registration via the Family Advocacy website here.

In Control Australia is a group of individuals and organisations who aim to bring about systemic policy change in Australia to enable individuals with disability and their families to manage their support. The organisation is an affiliate of In Control UK and works to provide an avenue for information exchange, critical inquiry, dialogue, collaboration, leadership and influence.

Family Advocacy workshops on schooling, supported living, future planning

Family Advocacy is offering a range of workshops for families over the next few months, including:
 
Let's get started... getting ready for school and life  (July and August)
This 3 hour workshop will provide information useful for families who would like their child with disability to attend an ordinary mainstream school, with appropriate support.

The workshop is being offered across metropolitan and regional NSW during July and August.

Practicalities of supported living (10th August)
Is it possible for a person with disability to have a home of their own without a full package of government funded support?

Planning for now, tomorrow and the future (11th September)
One of the most common concerns for families is the uncertainty about the future for their family member with disability.This workshop will identify the ways families can plan for and provide a secure future.

Click here to go to the Family Advocacy website for all details, dates, venues and to download fliers

"Now I See" book project - would you like to contribute?

The call for submissions for the Now I See book project are still open - contact the organisers now if you are interested in contributing:

Submissions are being sought from parents (both mums and dads) who have a child with Down syndrome and who are keen to write about their experiences: of how they dealt with their child’s diagnosis; of what they thought life would be like with their child and how, in reality, it has turned out to be; and the gifts (for instance, acceptance, respect, love, courage and delight) that child has brought into their lives.

The submissions will be compiled into a national book, with the working title Now I See. The book is aimed at raising awareness (and challenging outdated ideas) about life today for children with Down syndrome and their parents. All submissions will be considered. More information: www.nowisee.com.au

Monday, 28 June 2010

NSW Upper House inquiry into services provided or funded by ADHC

This inquiry is a current Legislative Council inquiry conducted by the Social Issues Committee. This inquiry was proposed by Mr Ian Cohen on 24 June 2010, to report on the quality, effectiveness and delivery of services provided or funded by the Department of Ageing, Disability and Home Care (ADHC).

Terms of reference, submission requirements and detail for public hearings are available from the inquiry's webpage.

Four public hearing days are scheduled at the Jubilee Room, NSW Parliament House, on 9th, 10th, 16th and 17th August 2010.
Submissions close: 6 Aug 2010

Final Report Due: 30 Sep 2010
 
Note:  this is a separate inquiry to the ADHC consultations referred to in this post. and this one, posted on 22/06/2010, and from the Ombudsman's current investigation into services for families of children with disabilities, referred to here.

Friday, 25 June 2010

Extension of Disability Care & Support Inquiry Deadline: to 16 August 2010

The Australian Government has asked the Productivity Commission to undertake a public inquiry into a long-term disability care and support scheme.

The Productivity Commission has extended the due date for initial submissions to 16 August 2010. Second and further submissions are welcome.

 

Amongst other things, this inquiry will examine:
  • how a scheme should be designed and funded to better meet the long-term needs of people with disability, their families and carers
  • how to determine the people most in need of support, the services that should be available to them, and service delivery arrangements
  • the costs, benefits, feasibility and funding options of alternative schemes
  • how the scheme will interact with the health, aged care, informal care, income support and injury insurance systems
  • its impacts on the workforce
  • how any scheme should be introduced and governed
  • what protections and safeguards should be part of the scheme.
More Information: www.pc.gov.au/projects/inquiry/disability-support

Thursday, 24 June 2010

Library Thursdays: Blueberry Shoes DVDs

The cold darkness of the winter solstice this week drew me to the DVD section of the library. It's a perfect time to settle down to a good film. We have great documentaries and fictional stories as well as informational ones. Next week we'll look at the stories but this week I'd like to remind you of the useful, educating and inspirational Blueberry Shoes series that Will Schermerhorn has done. The First 18 Months is well known by most new parents as the first thing suggested to be borrowed. It gives a view into babies with Down syndrome's development from birth to walking. You may want to revisit this film once the early months are past. Arabic, Chinese & Vietnamese translations are due out this month.
The next in the series is Discovery: Pathways to better speech for children with Down syndrome. Some of the chapters are available to view online.
Kids with Down syndrome: staying healthy and making friends includes information on toilet training, behaviour, sleep problems, hearing issues and other health and social topics.
What Did You Say?: A guide to speech intelligibility in people with Down syndrome is another Blueberry Shoes production. This features Libby Kumin discussing the factors that affect speech.

Will Schermerhorn has also created the wonderful Respect public service announcement which we have linked on the right on this blog.

He also has a link on his site to Sue Buckley's lectures done at for the Down Syndrome Association of West Virginia. Not all segments are available yet but there is an interesting question and answer segment that discusses special education and how to make inclusion work as well as other things. Notes from the sessions are also available to download.

Sue Buckley is currently giving many of the Down Syndrome Education International web seminars and online advice sessions. There is a special on the sessions until the end of June to buy one get one free. Also on sale until the end of June are the See and Learn kits and many of the DownsEd books and DVDs. The recordings of their free research briefings that have already taken place can be accessed from their Web events site. You need to click on "Event Recordings" under "Attend an event" on the left. The next live research briefing (on a study on interventions to improve thinking and problem solving skills) is on the 7th of July (9:30am BST, 6:30pm AEST (Sydney)) To register, click here.

If you'd like to borrow any of the Blueberry Shoes DVDs or anything else, just email or call.

Call to change disability bias of migration law

The media interest in Enabling Australia, the recently tabled report of the Inquiry into the Migration Treatment of People with Disability.  Today's Sydney Morning Herald includes an article by immigration correspondent, Yuko Narushima.

Wednesday, 23 June 2010

Migration Review and disability: LifeMatters podcast

The podcast of yesterday's LifeMatters (ABC Radio National) discussion of  Enabling Australia,  the report of the recent review of immigration policy as it impacts on people with disabilities and their families, is now available to listen to online, or to download as an mp3 file.  Richard Aedy interviewed the review's Chairman, Michael Danby, and the CEO of Down Syndrome Victoria, Catherine McAlpine.

The report itself is substantial (239 pages), and is available to download as a whole, or in chapters, from the Committee's webpage.

The Joint Standing Committee on Migration has made 18 recommendations aimed at  modernising the immigration treatment of people with disabilities,  but has fallen short of recommending that disability be removed from immigration health criteria.  

Senators Sue Boyce and Sarah Hanson-Young have made "additional comments" (pp 201 - 213), stating that ....

..... "we are of the view that the Inquiry provided sufficient evidence to warrant going further than Recommendation 18 to achieve a truly nondiscriminatory, and economically and socially beneficial, approach to migration treatment of disability." 

Their further recommendations are:

Recommendation A: We recommend that the Government remove the exemption of the Migration Act 1958 from the Disability Discrimination Act 1992.

Recommendation B: In the event that Recommendation A is not accepted, we recommend that the Government acknowledge that rejecting temporary visa holders as permanent visa holders solely on the basis of the birth of a child with a disability is discriminatory and develop protocols to address this.

Revised guidelines on cervical spine instability

The UK and Ireland Down's Syndrome Medical Interest Group has recently revised its guidelines on cervical spine instability (which includes atlantoaxial instability and other conditions) in people with Down syndrome, confirming its long established recommendation that X rays are too unreliable for screening purposes in people without symptoms.  This recommendation is in line with that of the Australian SpineCare Foundation issued in 2004.

The revision also makes clearer recommendations on "different priorities and courses of action for those who are symtomatic and those who are not".

The revised guidelines are intended for professional use.  It would be a useful document  (it is a single sheet) for people with Down syndrome to have in their medical files should it ever need to be referred to, or for families to provide their doctor with a link to the online file:  www.dsmig.org.uk/library/articles/CSI%20from%20BACCH%20newsletter.pdf

It is intended that the revised guidelines will be published by the DSMIG with "fully referenced background notes" later in the year.  The interim document was published by the British Association for Community Child Health, March 2010.

Those interested in the ongoing international differences in recommendations about the value of X-ray screening of people with Down syndrome without screening might be interested in a recent review by neurosurgeons from Columbia University in New York:

Hankinson, TC, Anderson, RC, Craniovertebral Junction Abnormalities in Down Syndrome, Neurosurgery, March 2010 - Volume 66 - Issue 3 - p A32–A38 
  • The abstract and options to purchase the full text of this paper are available here.
Both of these papers emphasise that where surgery is indicated, techniques have developed and improved considerably, and "increasingly good outcomes are being reported where timely intervention is performed in experienced centres" (DSMIG UK).  Hankinson and Anderson conclude that "..... Surgeons performing upper cervical and craniocervical fusion in children with DS should be highly familiar with the surgical anatomy of the region, as these patients frequently harbor congenital anomalies. High resolution imaging is a critical adjunct to successful operative planning."

Tuesday, 22 June 2010

Down and out in public health care limbo: letter to the editor

Adrienne Tunnicliffe's letter to the editor of the Sydney Morning Herald, published today, describes a too-familiar combination of circumstances for families of older people with Down syndrome - lack of availability of appropriate supported living options and an unprepared health system:

Like Barbara Grills, I care for a sister with Down Syndrome and Alzheimer's disease (''Dementia a huge challenge for Down carers'', June 21). Unfortunately, coping with the disability and this dreadful disease are not the only challenges such people face as they age. They, and those that care for them, must also negotiate a public health system that does not know what to do with them.

My sister has lived a productive and independent life in her own home. When it became obvious she could no longer cope alone, we faced and won an agonising battle to have her placed on an emergency waiting list for placement in a group home.

The Department of Ageing Disability and Home Care told us it would take more than a year to reach the top of the list. When her dementia was finally diagnosed as Alzheimer's this year, the department told us that due to the rapid progress of the disease in people with Down Syndrome, by the time she reached the top of the list the placement would no longer be appropriate and we would have to pursue placement in aged care, beginning with an aged care assessment.

The team we were referred to refused to assess her because she didn't meet the age criterion. She was left bouncing in limbo, with neither organisation accepting responsibility. Meanwhile, her carers and family waited for an inevitable crisis to occur. It did, and she was admitted through accident and emergency to Royal North Shore Hospital.

An aged care assessment was finally done, but the job of finding a suitable residential placement was given to the family. This task is heartbreaking, frustrating and demeaning. There is no suitable or appropriate placement for people with intellectual disabilities and early onset dementia.

Under increasing pressure from the hospital to relinquish an acute care bed, we accepted a respite place in an aged-care hostel. This will become permanent this month. The hostel is well run, caring, inclusive and willing to accept the challenges of her placement, but all the goodwill and care in the world cannot make it an appropriate solution.

My sister is a feisty and independent woman who has brought love into the life of everyone she has known. She only has a few years left, and she deserves better.

Adrienne Tunnicliffe, Roseville

Have your say about disability services: Stronger Together Consultations

Stronger Together: A new direction for disability services in NSW 2006-2016 is the NSW Government’s 10 year plan for disability services.

During June and July 2010 the Minister for Disability Services, Peter Primrose is hosting a series of consultations across the state to inform the next phase of Stronger Together.

A consultation paper has been developed which reports on what Stronger Together has achieved so far and which asks some key questions about planning, modelling and service delivery in NSW.

The NSW Government invites members of the community, who have an interest in improving disability services in NSW, to have input into the planning process by making a submission.

You can make a submission by:

• Responding to some of the key questions raised in the consultation paper online

• Emailing your comments to strongertogether@dadhc.nsw.gov.au  or

• Posting written comments to:

Stronger Together -  consultation feedback
Ageing, Disability and Home Care
Level 5, 83 Clarence Street
Sydney NSW 2000

Your submission must be received by 5.00pm 19 July 2010.

If you require the consultation paper in an accessible format or in Assyrian, Chinese (simplified), Chinese (traditional), Greek, Italian or Vietnamese please call (02) 8270 2140.

Source:  www.dadhc.nsw.gov.au

Have your say about disability services: Stronger Together Consultations 2

STRONGER TOGETHER 2 consultations – July dates for metropolitan and regional consultations.
Minister Primrose’s office has advised the dates and locations of these important consultations on the growth of disability supports and services for the next five years of the Stronger Together Disability Plan. Minister Primrose is intending to attend all of the consultations, which will inform proposals for disability funding in NSW. Venues and registrations will be advised shortly - contact your local ADHC office for details and to reserve a place.

Drummoyne consultation: Friday 25 June 2.00pm – 4.00pm
Narellan consultation: Monday 28 June 9.00am – 11.00am
Bathurst consultation: Wed 7 July 9.00am – 11.00pm
Dubbo consultation: Wed 7 July 3.00pm – 5.00pm
Gymea consultation: Thursday 8 July 9.00am – 11.00am
Wollongong consultation: Thursday 8 July 2.00pm – 4.00pm
Queanbeyan consultation: Friday 9 July 3.00pm – 5.00pm
Tamworth consultation: Wed 14 July 11.00am – 1.00pm
Parramatta consultation: Thursday 15 July 10.00am – 12.00pm
Chatswood consultation: Thursday 15 July 4.30pm – 6.30pm
Wagga Wagga consultation: Friday 16 July 11.00am – 1.00pm
Newcastle consultation: Monday 19 July 2.00pm – 4.00pm

Source:  NCOSS Ageing and Disability Updates, 17th June 2010

Monday, 21 June 2010

Immigration review - report to be tabled in Parliament

The report of the Australian Parliamentary Joint Standing Committee on Migration -  Immigration Treatment of Disability is scheduled to be presented to the House of Representatives tonight, by the Committee Chairman, Michael Danby (MP for Melbourne Ports).

The report is now available online here.

Catherine MacAlpine, CEO of Down Syndrome Victoria will be interviewed on Life Matters, Radio National (ABC) tomorrow morning (Tuesday 22nd June) at 9.05 am, about the report.

Click here for earlier posts about Immigration to Australia, and this review.

Dementia highlighted in press, new project for DS NSW

The increased incidence of dementia amongst older people with Down syndrome, and the challenges it poses,  was highlighted in an article by the Health Editor, Julie Robotham, in today's Sydney Morning Herald, accompanied by a lovely photo of Trevor Sweeney and his sister, Barbara Grills, which is unfortunately not on the article's web page.

The article also mentions a very welcome new one year grant to Down Syndrome NSW from the Australian Government, to develop information services for family and professional carers of people with Down syndrome and dementia.  The project is in the early planning stages, and details of resources and events will be announced shortly.

Clarification- Steve Clarke, CEO of Down Syndrome NSW did not actually say that establishing a baseline for people with Down syndrome in their 20s is "controversial" - it is well accepted that such a practice is useful, although there is no single, universally accepted assessment process.  Down Syndrome NSW supports appropriate assessment, at intervals as recommended by experts in the field. Those experts would also caution against over-assessment.

Down Syndrome and Alzheimer's Disease - Australian guidelines, published in 2009, available for free download.  Print copies are available free from Down Syndrome NSW - call our librarian, Kathi Beck, on 02 9841 4410, or email library@dsansw.org.au

Saturday, 19 June 2010

My Perspective: UK photography competition winners announced

The winners of the first DSA (UK) My Perspective photography competition were announced last night in London. The competition was open to photographers with Down syndrome. You can see the results here. 

Family Voices

Children with Disability Australia (CDA) is a newly launched national organisation (based in Melbourne) focusing on systemic advocacy for children with disabilities and their families, at the Federal level.  Many of the issues that CDA will address will be highly relevant for families of children with Down syndrome.

The CDA website is still under development, but they have published the first issue of their online magazine, Family Voices, that can be viewed on the website's home page. The first feature article is "Celebrating Sam", written by Deb Jeffris, about her son who has Down syndrome - Sam and his sister are also on the cover.

CDA membership is free for children with a disability and their families.

Thursday, 17 June 2010

Library Thursdays: Puberty and Special Girls

Puberty and Special Girls by Rose Stewart, Heather Anderson & Fay Angelo, 2009, is the authors' second book for girls with special needs. Special Girls' Business is known as THE book for explaining how to manage periods for girls with Down syndrome and other special needs. Puberty and Special Girls has a section on managing menstruation, but it also covers all aspects of puberty--body changes, hygiene, feelings, and sexuality. Illustrator Jeff Taylor has made the pictures a little more contemporary than in Special Girls' Business which may appeal more to that age group.

I think all the books by these authors are outstanding. If you just want a simple book on initially managing periods, I would look at Special Girls' Business. However, Puberty and Special Girls covers so much more that if I was only going to read one book, this would be the one although I can see that some might find it a bit too much information.

If you'd like to borrow Puberty and Special Girls or Special Girls' Business or any other resources in the library, just call or email.

Secret Girls' Business website

Other books by these authors:

Secret Girls' Business
More Secret Girls' Business
Special Boys' Business
Secret Boys' Business

Other useful materials:

Talk to Me - a personal development manual for women and girls with Down syndrome and their parents