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Content provided by Joe Woolworth and National MPS Society. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Joe Woolworth and National MPS Society 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.
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A Fierce Accessibility Advocate- Fanny Zambrano

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Manage episode 350815292 series 3320145
Content provided by Joe Woolworth and National MPS Society. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Joe Woolworth and National MPS Society 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.

In this episode:

  • Fanny shares her diagnostic journey to her diagnosis. She is from a large family in Chicago.
  • A large family meant a lot of family gatherings for Fanny, and she refused to let her mobility issues keep her from them. This is an issue that affects a lot of people with mobility issues, especially during the holiday season.
  • With her mother not speaking English, when Fanny was a child, she learned early to advocate for herself as she translated for her mother during doctor appointments.
  • Fanny shares her experience during college. She knew a large campus would be impossible for her, so she found a college in Texas where the building was only three floors and not as expansive as other campuses.
  • She shares about overcoming other people's perceptions. And how she learned to overcome her embarrassment of using a wheelchair.

The National MPS Society exists to cure, support, and advocate for MPS and ML.

If you like Our Voices, visit our website and follow us on social media on Facebook, Instagram, Twitter, and LinkedIn. And if you like the podcast, we'd appreciate you telling a friend (maybe even two).

  continue reading

17 episodes

Artwork
iconShare
 
Manage episode 350815292 series 3320145
Content provided by Joe Woolworth and National MPS Society. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Joe Woolworth and National MPS Society 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.

In this episode:

  • Fanny shares her diagnostic journey to her diagnosis. She is from a large family in Chicago.
  • A large family meant a lot of family gatherings for Fanny, and she refused to let her mobility issues keep her from them. This is an issue that affects a lot of people with mobility issues, especially during the holiday season.
  • With her mother not speaking English, when Fanny was a child, she learned early to advocate for herself as she translated for her mother during doctor appointments.
  • Fanny shares her experience during college. She knew a large campus would be impossible for her, so she found a college in Texas where the building was only three floors and not as expansive as other campuses.
  • She shares about overcoming other people's perceptions. And how she learned to overcome her embarrassment of using a wheelchair.

The National MPS Society exists to cure, support, and advocate for MPS and ML.

If you like Our Voices, visit our website and follow us on social media on Facebook, Instagram, Twitter, and LinkedIn. And if you like the podcast, we'd appreciate you telling a friend (maybe even two).

  continue reading

17 episodes

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