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Anna's Story of Hope and Help: FUS-ALS with Sonja Kämpfer and Dr. Neil Shneider

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Manage episode 418359434 series 3349924
Indhold leveret af n-Lorem Foundation and N-Lorem Foundation. Alt podcastindhold inklusive episoder, grafik og podcastbeskrivelser uploades og leveres direkte af n-Lorem Foundation and N-Lorem Foundation eller deres podcastplatformspartner. Hvis du mener, at nogen bruger dit ophavsretligt beskyttede værk uden din tilladelse, kan du følge processen beskrevet her https://da.player.fm/legal.

Stan Crooke speaks with Sonja Kampfer and Dr. Neil Shneider, associate professor of motor neuron disorders at Columbia Medical School, about Sonja’s daughter, Anna. Anna was diagnosed with an aggressive, fatal form of ALS at the age of 16. ALS is rare in teenagers, and this form of ALS is the worst of the worst. Sonja tells Anna’s story initial symptom onset, to diagnosis, and to Anna's response to ASO treatment. As a parent, Sonja reveals her full range of emotions during the duration of her daughter’s disease: puzzlement, pain, humility, and now optimism.

On This Episode We Discuss:

  • Anna’s life before her symptoms appeared
  • The road to a diagnosis and treatment– from Germany to New York City
  • Neil Shneider and his work with ASOs
  • The struggles of a family fighting a nano-rare disorder
  • Anna’s mutation
  • Anna’s remarkable progress

  continue reading

54 episoder

Artwork
iconDel
 
Manage episode 418359434 series 3349924
Indhold leveret af n-Lorem Foundation and N-Lorem Foundation. Alt podcastindhold inklusive episoder, grafik og podcastbeskrivelser uploades og leveres direkte af n-Lorem Foundation and N-Lorem Foundation eller deres podcastplatformspartner. Hvis du mener, at nogen bruger dit ophavsretligt beskyttede værk uden din tilladelse, kan du følge processen beskrevet her https://da.player.fm/legal.

Stan Crooke speaks with Sonja Kampfer and Dr. Neil Shneider, associate professor of motor neuron disorders at Columbia Medical School, about Sonja’s daughter, Anna. Anna was diagnosed with an aggressive, fatal form of ALS at the age of 16. ALS is rare in teenagers, and this form of ALS is the worst of the worst. Sonja tells Anna’s story initial symptom onset, to diagnosis, and to Anna's response to ASO treatment. As a parent, Sonja reveals her full range of emotions during the duration of her daughter’s disease: puzzlement, pain, humility, and now optimism.

On This Episode We Discuss:

  • Anna’s life before her symptoms appeared
  • The road to a diagnosis and treatment– from Germany to New York City
  • Neil Shneider and his work with ASOs
  • The struggles of a family fighting a nano-rare disorder
  • Anna’s mutation
  • Anna’s remarkable progress

  continue reading

54 episoder

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