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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 University Experience of Unnecessary Obstacles

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Manage episode 348364145 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:

  • At 18 months of age, Olivia was diagnosed with Hurler Syndrome (MPS IH). She has always been an overcoming and has overcome every obstacle in her path, and now at 18 years old, she has the opportunity to go to college.
  • Today we talk about Olivia's first semester at college and her being a trailblazer. And her parents' experience being advocates for not only her life but her career.
  • We talk about Olivia's high school experience and the joyful experience of getting into Mississippi State University.
  • After falling in love with interior design after an elective in high school, she decided to go to Mississippi State University because their motto is "Family," and they take care of their students.
  • Facing physical challenges in the classroom and after meeting with the disability resource center, Olivia started to fall behind because of a lack of accommodations.
  • "I've been fighting for her life for 18 years, I never thought I would have to fight for her career." Jamie.
  • After a frustrating meeting where Olivia was treated unfairly by college officials, Olivia left the meeting and called her parents and could not articulate what was happening. Her dad got in the car and started driving to the University. A parent's worst nightmare.

Let Olivia know that she is not alone in this fight, use the hashtag #WriteForOlivia to encourage her.

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 348364145 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:

  • At 18 months of age, Olivia was diagnosed with Hurler Syndrome (MPS IH). She has always been an overcoming and has overcome every obstacle in her path, and now at 18 years old, she has the opportunity to go to college.
  • Today we talk about Olivia's first semester at college and her being a trailblazer. And her parents' experience being advocates for not only her life but her career.
  • We talk about Olivia's high school experience and the joyful experience of getting into Mississippi State University.
  • After falling in love with interior design after an elective in high school, she decided to go to Mississippi State University because their motto is "Family," and they take care of their students.
  • Facing physical challenges in the classroom and after meeting with the disability resource center, Olivia started to fall behind because of a lack of accommodations.
  • "I've been fighting for her life for 18 years, I never thought I would have to fight for her career." Jamie.
  • After a frustrating meeting where Olivia was treated unfairly by college officials, Olivia left the meeting and called her parents and could not articulate what was happening. Her dad got in the car and started driving to the University. A parent's worst nightmare.

Let Olivia know that she is not alone in this fight, use the hashtag #WriteForOlivia to encourage her.

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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