This month, we’re highlighting the inspiring story of Pia Asthana, one of our passionate Celiac Disease Foundation advocates! Pia’s dedication to raising awareness for celiac disease and driving meaningful change…
Continue ReadingThis month's story comes from Brett Spitale, CDF's Chief of Staff, and special guest appearance from his son, Maxwell!
Continue ReadingThis 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 story!
Continue ReadingThis month's story comes from Dan Gibbons, a patient advocate who also happens to be the Foundation's newest board member!
Continue ReadingThis month we hear from Sonia, the mother of a young celiac disease patient. Thank you, Sonia for sharing your family's story!
Continue ReadingThis month we hear from Sanjith Senthil, one of our younger advocates with a strong dedication to improving the lives of celiac disease patients.
Continue ReadingEach month in our advocacy newsletter, the Celiac Disease Foundation highlights one of our many dedicated advocates as part of our Patient Profile Series.
Continue ReadingAn important part of building community among our patients, caregivers, and supporters throughout the country is through elevating the good work our advocates are engaged in!
Continue ReadingLast month, the Celiac Disease Foundation had the privilege of sponsoring the 2024 International Celiac Disease Symposium in Sheffield, UK. As the first patient advocate invited to chair and present on a scientific panel, CEO Marilyn Geller co-chaired the End Points in Clinical Trials session with Dr. Francisco Leon, CEO...