Each month in our newsletter, the Celiac Disease Foundation highlights one of our many dedicated advocates as part of our Patient Profile Series. These advocates display their passion by raising awareness for celiac disease in their local communities and participating in nationwide efforts to support federal policy changes. This month’s story comes from Janie Magill, a patient advocate who also happens to be the Celiac Disease Foundation Director of Development. Thank you, Janie!
Would you like to share your story? Please email us at [email protected] – we hope to hear from you soon!
Janie’s video also highlights our annual 2023 Turkey Trot – a virtual event that is fun for the whole family. For more information and to register for the event, please visit this link: 2023 Turkey Trot | Celiac Disease Foundation
