In this episode of "Living Ultra Rare," host Paul Biderman interviews Yoyo, a Caltech undergraduate studying biology and chemistry.

Yoyo discusses her research on rare diseases, particularly Abetalipoproteinemia (ABL), and her participation in the Harvard Rare Disease Hackathon.

Yoyo highlights the challenges of diagnosing ABL, the importance of early intervention, and her current project with the ABL Plus Foundation aimed at incorporating ABL into newborn screening panels.

This episode underscores the significance of early diagnosis and community collaboration in improving outcomes for rare disease patients.

Today we speak with Joe who has a rare disorder called

Today we have our first interview relating to Chylomicron Retention Disorder as we speak to Riley about her son Luca. Luca was diagnosed as a baby when nurses noticed that he has a unique set of symptoms.

Dr. Cindy Bredefeld joins us to discuss how the body's inability to process certain lipids properly causes issues in patients with ABL, FHBL, and CMRD.

Paul is headed to Washington DC for the National Organization or Rare Disorders.

To learn more about The ABL+ Foundation and to donate please visit https://www.ablfoundation.org/donate

Meet Ann Marie and her daughter Aimee, raising Louis, a precocious seven year old with Abetalipoproteinemia.

To learn more about The ABL+ Foundation and to donate please visit https://www.ablfoundation.org/donate

Meet Noah. She's a poet in her twenties living with Abetalipoproteinemia. A rare disease doesn't slow her down though. She's making the best of her life.

To learn more about The ABL+ Foundation and to donate please visit https://www.ablfoundation.org/donate