Welcome, and thank you for visiting Supporting Aussie Kids with Kabuki Syndrome Incorporated.

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SAKKS is a voice for Kabuki Syndrome, and if you are visiting for the first time because your child has been recently diagnosed with Kabuki Syndrome, know that you are not alone.


Kabuki Syndrome is rare, and a difficult journey for our parents, remember, a diagnosis gives answer to the symptoms your child experiences, not the person your child is or will become.

Every parent will deal with a diagnosis differently, and even though Kabuki Syndrome is a relatively new syndrome, Geneticists and Counsellors have heard of the Syndrome and can offer support. Many General Practitioners aren’t usually aware of Kabuki Syndrome, however they are always keen to learn more, as are other health care providers, and we offer plenty of information on our site to assist with this.

To help support those affected by Kabuki Syndrome, we, (Peta and Adrian), created this website in 2004. We hope to offer comfort and support to other families just like ours. By joining our membership you will receive the latest information, newsletters and contact with other parents.


“When we found out our son had Kabuki Syndrome we were devastated, our lives seem to come to a crashing halt. We felt so supported when we reached out to SAKKS, and the friendships and information made a huge difference, thank you from the bottom of our hearts.” Stacey and Darrin (Victoria)



Who is Supporting Aussie Kids with Kabuki Syndrome? 

We are a registered not for profit charity who support families/caregivers who have a child with Kabuki Syndrome. We offer information, external links to genetics departments and research as well as links to medical information. A stories page with personal accounts describing many of the challenges of coping with a child that has Kabuki Syndrome. We also display members photographs, facilitate contact with other parents, sibling information, early Intervention and educational links... and of course - support. We host 3 day retreats, educational seminars and family days for families who have a child with Kabuki Syndrome. Membership for family members including siblings and membership for professionals to aide in information sharing. SAKKS currently has over two hundred members from every corner of the globe.


Our Key Objectives: 

  • To celebrate the achievements of all children and adults with Kabuki Syndrome
  • To support families/caregivers by offering information, friendship and contact with other families
  • To provide information to the public; raise awareness
  • To provide information to the educational and medical sectors to increase awareness and aide in earlier diagnosis
  • To support the siblings of children with KS giving an opportunity to talk with other siblings in similar situations


SAKKS is only successful because of its members – and we say thank you to those who have become members and supplied stories and photographs.

"Difficult roads often lead to beautiful destinations."


Thankyou for visiting www.sakks.org




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A Dream come true for Jack

Click here to find out what happened...

Josh is a Superhero

Kabuki syndrome sufferer Josh Concilia shows the world he’s as tough as they come. Read the story here.

Sophie learns to ride

Horse rider Linda Gaffaney overcomes serious injury to teach at riding school for the disabled. Read the story here.

Ollie's Family & Friends to race

Three-year-old Ollie McKinnon has Kabuki syndrome and his family and friends will race in Herald Sun’s Run for the Kids. Read the story here.

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