# "There’s Nothing We Can Do” Isn’t Okay: A Mother’s Fight for Rare Disease Gene Therapy

Page: https://stenobird.com/podcast/speak-up-for-your-health-6687973/there-s-nothing-we-can-do-isn-t-okay-a-mother-s-fight-for-rare-disease-gene-therapy
Text version: https://stenobird.com/podcast/speak-up-for-your-health-6687973/there-s-nothing-we-can-do-isn-t-okay-a-mother-s-fight-for-rare-disease-gene-therapy.md
Podcast: [Speak Up For Your Health](https://stenobird.com/podcast/speak-up-for-your-health-6687973)
Published: 2026-01-20T09:12:00+00:00
Episode link: https://www.podtrac.com/pts/redirect.mp3/traffic.megaphone.fm/DHT3195684125.mp3
Audio file: https://www.podtrac.com/pts/redirect.mp3/traffic.megaphone.fm/DHT3195684125.mp3
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JSON: https://stenobird.com/v1/public/podcasts/speak-up-for-your-health-6687973/episodes/there-s-nothing-we-can-do-isn-t-okay-a-mother-s-fight-for-rare-disease-gene-therapy
Duration seconds: 1783

## Resource

What happens when a parent refuses to accept “there’s nothing we can do” for a child with a rare disease? In this episode of Speak Up For Your Health, Archelle Georgiou speaks with Amber Olsen and filmmaker Patrick O’Connor about their new documentary, The Zebra and the Bear—and a mother’s seven-year fight to advance gene therapy for a rare disease. Amber’s daughter, Willow, was diagnosed at age two with Multiple Sulfatase Deficiency (MSD), an ultra-rare, progressive genetic condition with no known treatment. Instead of stopping there, Amber spent the next seven years learning the science, raising funds, and advocating relentlessly to support research that could one day change the outcome for other children. Documentary filmmaker Patrick O’Connor followed Amber and her family throughout that journey, capturing what happens when parents are forced to become advocates, fundraisers, and drivers of medical research. Together, they discuss the emotional moment Amber learned her efforts helped move MSD research to the point where the National Institutes of Health selected it for a pilot gene-therapy program—a milestone filled with both hope and heartbreak. Key Takeaways The key takeaways from this episode extend well beyond Multiple Sulfatase Deficiency and may be especially helpful for parents caring for a child with a serious rare or chronic illness: • Being told “there’s nothing we can do” doesn’t have to be the end of the conversation. Asking questions and seeking options is not denial—it’s loving your child. • You don’t need to be a clinician or a scientist to advocate for your child.Asking the right questions opened doors she didn’t know existed. • Many experts want to help—sometimes you just have to reach out.Access to scientists and research often starts with a direc…

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