Patient Empowerment Program: A Rare Disease Podcast

Patient Empowerment Program: A Rare Disease Podcast

n-Lorem Foundation (Dr. Stan Crooke, Amy Williford, Kim Butler, Andrew Serrano, Jon Magnuson, and Kira Dineen)

Join the nano-rare disease community! Interviews features leading physicians, scientists, biotech experts, and patient advocates. Lessons teach core concepts about drugs. Our host Dr. Crooke has led the creation of antisense technology and his foundation, n-Lorem, is using this powerful technology to discover, develop, and provide personalized experimental antisense oligonucleotide medicines to nano-rare patients for free, for life.

n-Lorem is a non-profit organization established to apply the efficiency, versatility and specificity of antisense technology to charitably provide experimental antisense oligonucleotide (ASO) medicines to treat patients (less than 30 patients) that are the result of a single genetic defect unique to only one or very few individuals. The advantage of experimental ASO medicines is that they can be developed rapidly, inexpensively and are highly specific. n-Lorem was founded by Dr. Stan Crooke, who founded IONIS Pharmaceuticals in 1989 and, through his vision and leadership, established the company as the leader in RNA-targeted therapeutics.

The podcast is produced by n-Lorem Foundation and hosted by Dr. Stanley T. Crroke, who is the Founder, CEO and Chairman. Our videographer is Jon Magnuson. Our producers are Kira Dineen, Jon Magnuson, Kim Butler, and Amy Williford. To learn more about n-Lorem, visit nlorem.org. Contact us at podcast@nlorem.org.

Where can you listen?

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Episodes

Questions & Answers

How many episodes are there of Patient Empowerment Program: A Rare Disease Podcast?

There are 63 episodes avaiable of Patient Empowerment Program: A Rare Disease Podcast.

What is Patient Empowerment Program: A Rare Disease Podcast about?

We have categorized Patient Empowerment Program: A Rare Disease Podcast as:

  • Health & Fitness
  • Science
  • Medicine
  • Life Sciences

Where can you listen to Patient Empowerment Program: A Rare Disease Podcast?

Patient Empowerment Program: A Rare Disease Podcast is available, among others places, on:

  • Spotify
  • Apple Podcasts
  • Podtail
  • Google Podcasts

When did Patient Empowerment Program: A Rare Disease Podcast start?

The first episode of Patient Empowerment Program: A Rare Disease Podcast that we have available was released 16 May 2022.

Who creates the podcast Patient Empowerment Program: A Rare Disease Podcast?

Patient Empowerment Program: A Rare Disease Podcast is produced and created by n-Lorem Foundation (Dr. Stan Crooke, Amy Williford, Kim Butler, Andrew Serrano, Jon Magnuson, and Kira Dineen).