Search a title or topic

Over 20 million podcasts, powered by 

Player FM logo
Artwork

Content provided by Joanna. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Joanna 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://podcastplayer.com/legal.
Player FM - Podcast App
Go offline with the Player FM app!

Partial Trisomy 8Q Duplication Syndrome Wuth Saida From California

31:07
 
Share
 

Manage episode 513040770 series 3485028
Content provided by Joanna. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Joanna 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://podcastplayer.com/legal.

Send us a text

In this powerful episode of Rare Connection, Joanna Ball speaks with Saida Mahoney — a beauty queen, author of nine books, athlete, performing artist, and National Rare Disease and Disability Advocate living with Partial Trisomy 8q Duplication Syndrome, an ultra-rare genetic condition.

Saida shares her journey growing up with neurological challenges and multiple types of epilepsy, including focal, grand mal, idiopathic, and absence seizures. Her story is one of resilience, faith, and advocacy — showing the world that rare disease and disability don’t define a person’s worth or strength.

💜 Topics Discussed:

  • Living with Partial Trisomy 8q Duplication Syndrome
  • Navigating life with epilepsy and neurological symptoms
  • The importance of epilepsy awareness in the rare disease and IDD communities
  • Finding identity and purpose through advocacy
  • Using creativity, education, and pageantry to empower others

📚 Saida Mahoney’s eBooks on Wattpad

Explore Saida’s inspiring writing and advocacy through her online books:

Support the show

  continue reading

64 episodes

Artwork
iconShare
 
Manage episode 513040770 series 3485028
Content provided by Joanna. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Joanna 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://podcastplayer.com/legal.

Send us a text

In this powerful episode of Rare Connection, Joanna Ball speaks with Saida Mahoney — a beauty queen, author of nine books, athlete, performing artist, and National Rare Disease and Disability Advocate living with Partial Trisomy 8q Duplication Syndrome, an ultra-rare genetic condition.

Saida shares her journey growing up with neurological challenges and multiple types of epilepsy, including focal, grand mal, idiopathic, and absence seizures. Her story is one of resilience, faith, and advocacy — showing the world that rare disease and disability don’t define a person’s worth or strength.

💜 Topics Discussed:

  • Living with Partial Trisomy 8q Duplication Syndrome
  • Navigating life with epilepsy and neurological symptoms
  • The importance of epilepsy awareness in the rare disease and IDD communities
  • Finding identity and purpose through advocacy
  • Using creativity, education, and pageantry to empower others

📚 Saida Mahoney’s eBooks on Wattpad

Explore Saida’s inspiring writing and advocacy through her online books:

Support the show

  continue reading

64 episodes

Alle episoder

×
 
Loading …

Welcome to Player FM!

Player FM is scanning the web for high-quality podcasts for you to enjoy right now. It's the best podcast app and works on Android, iPhone, and the web. Signup to sync subscriptions across devices.

 

Copyright 2025 | Privacy Policy | Terms of Service | | Copyright
Listen to this show while you explore
Play