Each month, the Celiac Disease Foundation proudly shines a spotlight on one of our remarkable patient advocates as part of the Patient Profile Series. These advocates exemplify unwavering dedication by raising awareness of celiac disease within their local communities and actively engaging in nationwide campaigns. This month, we feature a heartfelt narrative from Brett Spitale, our new CDF Chief of Staff, accompanied by his son, Maxwell! Thank you to Brett and Maxwell for sharing their inspiring story with us.

Would you like to share your story? Please email us at [email protected] – we hope to hear from you soon!