Supporting families living with Phelan-McDermid Syndrome, the very rare genetic condition resulting from a deletion, translocation or other structural change in Chromosome 22. PMS currently affects approximately only 90 people in Australia & New Zealand (around 2100 worldwide), & is associated with autism, intellectual disabilities, global development delays, sleep disorders and seizures. PMSFA brings families together and supports them through their PMS journey. Your valued donation will assist PMSFA with funding & organising national conferences, bringing international experts to meet and consult with families, hosting family gatherings, maintaining online support forums, and in the future, to fund and guide local research into the syndrome in order to improve the quality of life for those afflicted.