Phelan-McDermid Syndrome Foundation Australia Stories

Olivia’s Story

25 October 2014

Just under 6 years ago our little miss was diagnosed with Phelan-McDermid Syndrome. We received a call from the Paediatrician in October 2011. Olivia's test had come back and we needed both Andrew & myself as well as a support person to meet . . . (read more)


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PMSF worldwide membership is for immediate family members and carers of children/adults diagnosed with Phelan-McDermid Syndrome.

This membership is free and allows you to be connected to people in your local area.

Once you have registered, a Regional representative will be in contact to arrange your welcome pack and you will begin to receive regular newletters from the worldwide PMSF.

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