SWAN Australia is a not for profit charity which provides information and support to parents/carers who do not have a genetic diagnosis for their child's/children's medical condition. We advocate for better resources and more funding into research to assist more children get a genetic diagnosis.
Who can Join
Anyone approved by the SWAN committee Ideally parents/carers and their friends and family and medical and educational professionals
Monday - Friday, 9.00 am - 5.00 pm. If the matter is urgent outside these times, please leave a message.
Where we meet
PO Box 390
Phone support Email & online support Meetings Networking opportunities Newsletter Information kits Fact sheets Peer support Guest speakers Seminars Workshops Friendship Social outings Personal or other advocacy Social action
We welcome new members.
Parents/Carers who do not have a genetic diagnosis for their child's medical condition or parents/carers who have a child with an extremely rare condition for which there is no support group.