Eosinophilic Awareness Month ended with our gratitude for support. Through Eosinophilic Voices and collaborations, we raised awareness and facilitated early recognition of symptoms. Your support is vital in achieving our mission for prompt diagnosis, treatment, and holistic care for EAD patients. Read more
Celebrate European Eosinophilic Oesophagitis Day, raising awareness of EoE and dysphagia. Learn about eosinophilic diseases, challenges in diagnosis and treatment, and initiatives to improve patients' lives. Read more
On May 18th, we celebrate Eosinophilic Associated Diseases EADs to bring attention to these rare life-impacting conditions. Learn about EAD symptoms, management, and how EOS Network advocates for improved care. Read more
I'm supporting EOS Network - a charity that helps people with a type of rare blood disease that makes it painful to eat. It is a small charity but is making a huge difference to thousands of people across the world. Read more
Due to the success of 2022, we have decided to extend our 2023 Eosinophilic Awareness Campaign to the whole month of May!
Below you will find resources and insights related to #EAM2023 that can be utilised throughout the year, anywhere in the world.
You are sure to find something you would like whether you're looking to participate or simply broaden your knowledge.
Consider exploring:
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
Check out our range of EOS Network goodies including T-shirts, Sweatshirts and Bags every purchase helps support people with Eosinophilic Diseases. Wear yours with pride! 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
Explore easy and engaging fundraising ideas and get involved to help people with eosinophilic gastrointestinal diseases eat without pain! 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
Help us to spread awareness among your fellow healthcare professionals by participating in our Think EoE campaign. Register for our pack of resources to help educate others to recognise the symptoms. Read more