I am fundraising to help my youngest son George and others like him who have been diagnosed with Eosinophilic Colitis a rare gastrointestinal disease. Read more
EOS Network is an important small charity that relies on fundraising to enable it to continue supporting EOE patients Read more
EOS Parents / Family / Carers Community Chat Wednesday 12th May - an informal zoom event giving an opportunity to meet and chat with others living with Eosinophilic Gastrointestinal Diseases Read more
For National Eosinophilic Awareness Week 2021 we are challenging our community to walk ≥15,000 steps to raise funds to improve diagnosis times and support for patients and families to live with eosinophilic diseases. Read more
EOS Adult Patients Community Chat Wednesday 5th May - an informal zoom event giving an opportunity to meet and chat with others living with Eosinophilic Gastrointestinal Diseases Read more
March's Wellbeing Wednesday sessions will provide an overview of Eosinophilic Oesophagitis (EoE), from allergy and gastroenterology. Suitable for patients, families and healthcare professionals. Read more
Our patient and carer community Wellbeing Wednesday virtual meet-ups will continue in February, and will feature presentations and Q&A sessions from dietitans for both adult and paediatric patients with EoE. Read more
Nov 2020 - We were proud to speak at the EUREOS Eosinophilic Gastrointestinal Diseases Symposium in October, with our Chair Amanda Cordell presenting on the Patient Perspective of living with EoE. Read more
Oct 2020 - RAREfest20 is an interactive event on the 28th November celebrating the stories, science and organisations improving the lives of people with rare diseases. Read more
Oct 2020 - This year's Student Voice Prize information, questions. details on how to apply and the prizes. Read more