Every person's eosinophilic journey is their own but with common challenges.
We thank everyone that has taken the time to share their story
To share your Eosinophilic voice contact us
Pennie, an artist with EoE, experienced symptoms from childhood. Her diagnosis was late but brought relief through diet and treatment. She advocates for EoE awareness and early diagnosis. Read more
Read Becky's story she shares as a young person living with Eosinophilic Oesophagitis. Despite challenges and additional diagnoses, she found support and resources in EOS Network and is hopeful about her future. Read more
Meet Jake, who's been fighting Eosinophilic Associated Diseases (EADs) since infancy. His inspiring journey, made possible by his family, healthcare professionals and the EOS Network, shows the power of informed patient advocacy. Read more
Stella shares her 50-year journey of symptoms to diagnosis of Eosinophilic Oesophagitis EoE and is passionate about helping people to get the right diagnosis quickly. She is a valuable member of our community, fundraising and a long-serving advocate. Read more
Sean Goss is a professional footballer with EoE. His journey will be familiar to many living with the condition - adapting lifestyle and struggling to find a correct diagnosis. We're proud to have him as an ambassador for our charity. Read more