Two years of treatment—two years of strength, courage, and blazing a trail for other nano-rare patients! 🎉 Susannah's story was the first shared on the Patient Empowerment Program podcast. Now, two years later, her father, Luke Rosen, and her physician, Dr. Jennifer Bain, detail Susannah’s remarkable progress since beginning regular treatments—highlighting improvements in her motor skills, cognition, energy, and more!

Susannah's Story (May 25, 2022)

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2024 Nano-rare Patient Colloquium

On This Episode We Discuss:

• 3:10 Susannah's KIF1A mutation