Kate Gough

The Patient Voice Podcast

Kate Gough is a passionate advocate and parent, dedicated to raising awareness and heralding improvement for those who are born with Spinal Muscular Atrophy (SMA) and their families.
As the mother of baby Oakley, who was diagnosed with SMA at eight weeks old, Kate brings a personal perspective to her advocacy work, striving to improve the lives of those with SMA and their families by calling for research and treatment advancements, as well as directly bringing about change by advocating for access to SMA screening in QLD.
Move For Oakley Facebook https://www.facebook.com/oakleysSMAadventures
Move For Oakley Instagram https://www.instagram.com/moveforoakley/
Our work at Patient Voice Initiative is only possible thanks to the generous support of our Sponsors; for a full list of both our Gold and Silver contributors, please visit our Website.

Find out more about PVI by visiting our website https://www.patientvoiceinitiative.org/

Produced by The Podcast Boss