In this episode of CareLab, we hear a mother's incredible story of resilience, hope, and the relentless pursuit of a cure for her daughter. Amber Olson shares her profound journey as a caregiver for her daughter Willow, who was diagnosed with multiple sulfatase deficiency (MSD), a rare and fatal genetic condition. Amber discusses the emotional and physical toll of caregiving, the challenges of navigating the healthcare system, and her efforts to create hope through the United MSD Foundation. She highlights the importance of community support, the need for open conversations about end-of-life care, and the ongoing fight for clinical trials to develop treatments for rare diseases.Support the fight to cure MSD at https://curemsd.org/Find Care Equipment solutions at https://www.asksamie.com/Learn about the future of care navigation at https://meetluma.us/https://www.carelabpodcast.com/Disclaimer: The following CareLab podcast does not provide health or medical advice. All content is provided for informational purposes only. Listeners are encouraged to speak with their healthcare provider for specific healthcare advice, and are wholly responsible for the outcome of implementing any tips or information presented.

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