Registered Charity No
EOS Network is the only UK charity supporting people affected by Eosinophilic gastrointestinal diseases. Founded as an online family support group in 2005 today we collaborate with over 200 global medical professionals and researchers to improve the lives of those affected by these chronic life impacting diseases.
We are a small volunteer team, we receive NO government funding and rely entirely on donations and grants to fund our work.
Is of a world where everyone with an Eosinophilic Gastrointestinal Disease can eat without pain.
Is to ensure that every person with an Eosinophilic Gastrointestinal Disease receives a prompt accurate diagnosis, the right treatment for them, and support to live with their condition.
What we do
- We provide information and support for people with Eosinophilic Gastrointestinal Diseases their families and carers, through our community hub, resources and events.
- We provide a global platform for clinicians and researchers to connect and share the latest research and best evidence-based practice.
- We provide educational resources and events for healthcare professionals to help them recognise symptoms, diagnose and treat Eosinophilic Gastrointestinal Diseases.
- We work with patients and their carers, medical bodies, manufacturers and funders to ensure the patient’s voice is heard for decisions about treatment guidelines, the development and availability of medicines.
“Both published evidence and our community data shows it currently takes an adult an average of over 8 years living with eating difficulties before getting a diagnosis of Eosinophilic Oesophagitis, your support will help us change this.”
Amanda Chair and Founder of EOS Network
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For more information about Eosinophilic Gastrointestinal Diseases and our work please visit us at www.eosnetwork.org or email [email protected]