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Kate Gough

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Manage episode 425992296 series 3525766
Content provided by The Patient Voice Initiative. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by The Patient Voice Initiative or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

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

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9 episodes

Artwork
iconShare
 
Manage episode 425992296 series 3525766
Content provided by The Patient Voice Initiative. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by The Patient Voice Initiative or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

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

  continue reading

9 episodes

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