Each month in our newsletter, the Celiac Disease Foundation highlights one of our many dedicated patient 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 Vanessa Weisbrod, CDF’s Chief Education and Community Engagement Officer, and her son Brandon. Thank you, Vanessa and Brandon, for sharing your stories!

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