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Life with rare, incurable disease is all about quality
Podcast |
Where We Live
Media Type |
audio
Categories Via RSS |
Government
News
Society & Culture
Publication Date |
Nov 30, 2022
Episode Duration |
00:48:30

One in ten Americans, or one on every elevator and four on every bus, FAQ-2019.pdf">is impacted by a rare disease. Yet, 95 percent of rare diseases do not have approved treatment. On a promising note, bio-pharmaceutical companies working on orphan drugs have more than 800 projects in clinical development.

In a ground-breaking clinical trial, a participating patient at the University of Connecticut Health Center was the first in the world to receive an infusion treatment for a type of glycogen storage disease.

This hour on Where We Live, we hear from the National Organization for Rare Disorders (NORD) on efforts to create a Rare Disease Advisory Council in Connecticut to elevate the voices of residents with rare diseases, something other states have done.

We also hear from a UConn researcher, and a father and son living with osteogenesis imperfecta, or brittle bone disease, on the latest treatment and challenges.

GUESTS:

  • John D'Alessandro: Diagnosed with osteogenesis imperfecta at age 40
  • Christian D'Alessandro: Diagnosed with osteogenesis imperfecta at around four weeks
  • Alicia Lawrence: Patient Services Case Manager, National Organization for Rare Disorders (NORD)
  • Amber Barry, RN: Glycogen Storage Disease & Disorders of Hypoglycemia Program at the University of Connecticut Health Center, and Connecticut Children’s Medical Center

Cat Pastor contributed to this show which originally aired February 23, 2022.

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