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

EPISODE · May 15, 2024 · 43 MIN

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

from Patient Empowerment Program: A Rare Disease Podcast

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

Episode metadata supplied by the publisher feed · Published May 15, 2024

Embed this episode

Ready to play

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

0:00 43:06

No transcript for this episode yet

We transcribe on demand. Request one and we'll notify you when it's ready — usually under 10 minutes.

No similar episodes found.

No similar podcasts found.

Frequently Asked Questions

How long is this episode of Patient Empowerment Program: A Rare Disease Podcast?

This episode is 43 minutes long.

When was this Patient Empowerment Program: A Rare Disease Podcast episode published?

This episode was published on May 15, 2024.

Can I download this Patient Empowerment Program: A Rare Disease Podcast episode?

Yes. Use the download control on the episode player to save the publisher-provided media file.
URL copied to clipboard!