SWAN Disability Transition Conference

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SWAN Disability Transition Conference features a number of speakers with lived experience of caring for a child with a disability.

About this event

Please join us for our virtual SWAN Disability Transition Conference through Zoom. Our conference features several speakers talking on a variety of topics, including ECIS, kinder, school, disability supports, puberty and post-school options. Our full conference program will be available shortly and sent in advance to all registered participants.

Although our conference runs from 10:00 am – 5:00 pm, you may just tune in to the sessions that are of interest to you. The conference will be recorded and be available for a limited time only for those who register for this event.

The cost to register for our conference is $100 per family, which is fully subsidised by SWAN thanks to us receiving grant funding from the Australian Government (so in effect, this conference is free for you to attend)

RSVP: Wednesday, 16 June, by registering for this event, noting any access requirements you may have.

Pre-conference Dinner (not included in conference fee)

Please note that our pre-conference dinners are not subsidised by any grants but are kindly supported by the limited donations we receive. We, therefore, ask that SWAN members contribute $10.00 per person to the cost of attending our pre-conference dinner. If you are experiencing financial hardship, please email, and we will assess each request on a case-by-case basis. Please not the option to attend our pre-conference dinner is only available to SWAN parents and SWAN full time carers.

Please click on the hyperlinked places below to register for dinner in the area closest to you.

Adelaide, Brisbane, Canberra, Gold Coast, Hobart, Launceston, Melbourne, Newcastle, Perth, Sydney

If you have any questions, please do not hesitate to contact Heather at SWAN: 0404 280 441 or email

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Organiser Syndromes Without A Name (SWAN) Australia

Organiser of SWAN Disability Transition Conference

Supporting families caring for a child with an undiagnosed or rare genetic condition.

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