20: Interview with Nick & Shanna Quimby

19/11/2024 34 min Temporada 1 Episodio 20
20: Interview with Nick & Shanna Quimby

Listen "20: Interview with Nick & Shanna Quimby"

Episode Synopsis

Take a moment to imagine the unimaginable. Imagine being told that your three year old child has a rare disease that will very likely result in death. You can slow the progression of the disease, but unfortunately it’s too late for any type of treatment to cure the disease or stop the progression. This unimaginable situation was the new reality for Nick & Shanna Quimby and ultimately resulted in the devastating loss of their son Gavin when he was five.They turned this unimaginable and devastating situation into a mission to help other families facing something similar. Their tireless efforts have led to the expansion of the newborn screening list and the Minnesota Rare Disease Advisory Council. But they won’t stop until their dream of getting MLD added to the newborn screening list is fulfilled. They also started the Gavin Quimby Research Fund at the University of Minnesota to support research and gene therapy for kids. If interested, you can donate to the Gavin Quimby Research Fund by mailing a check to the address below. Miller Scrap & Disposal is also making a donation to the Gavin Quimby Research Fund for every new customer who signs up for Miller Disposal's local trash service during the month of November.Nick and Shanna's efforts in memory of their son Gavin are already helping save lives here in Minnesota and across the country. Gavin Quimby Research Fund Dr. Troy LundMMC 366420 Delaware St SE Minneapolis, MN 55455Make checks payable to: “University of Minnesota Foundation.”Memo: ALD Research Fund UMF 11967Thank you for listening to Scrap Guy Solutions. We appreciate you! Please feel free to get in touch by sending an email to [email protected] or check out ScrapGuySolutions.com.Make today your day. Figure out what you want, then get started, stick with it, and go make it happen!