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EPISODE · Mar 13, 2025 · 27 MIN

My Mother, Myself, and ALS

from RARECast

Raziel Green lost both her mother and aunt to the rare neurodegenerative disease amyotrophic lateral sclerosis or ALS. But when Green, a runner, began experiencing muscle weakness and falls, doctors failed to recognize that she had a genetic form of the condition. Two years after she first sought care, she was diagnosed with the SOD1 form of the disease and enrolled in a clinical trial of what would become the antisense oligonucleotide Qalsody. We spoke to Green about her experience with ALS, her decision to enroll in a clinical trial, and her health more than eight years after her diagnosis.

Episode metadata supplied by the publisher feed · Published Mar 13, 2025

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Raziel Green, an ALS patient advocate, discusses her experience with the condition, her decision to enroll in a clinical trial, and her health more than eight years after her diagnosis.

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My Mother, Myself, and ALS

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