We are delighted to introduce Glue Ear Together (GET). Working together with families, education and health, we aim to provide clear, up-to-date information that promotes positive outcomes for children with glue ear.
The Glue Ear Together website (, developed with funding from the Ovingdean Hall Foundation, provides clear information about the cause of glue ear, common signs and symptoms, impacts on development, and interventions recommended by the National Institute of Clinical Excellence (NICE). We鈥檝e already have had a fantastically positive response to our 鈥楬elp me hear鈥� – ways to support a child with glue ear鈥� 聽page, which contains clear information about the simple steps that can be taken to help a young child to hear. We are driven by our belief that by empowering parents and early years practitioners with information about the impact that glue ear can have on wellbeing, they will have the confidence to take action to help.
Our aim is that the GET website will be a key resource for clinicians to signpost families to, promoting understanding of what was discussed in their child鈥檚 appointment. For professionals such as Teachers of the Deaf, Speech and Language Therapists and Health Visitors, we hope it will prove a useful resource for supporting families. We are very pleased that our website was approved for featuring in the 鈥業nformation for the public鈥� section of the new NICE guidelines for Otitis media with effusion in under 12s.
We鈥檇 be delighted if you would visit our website and consider how you can share it with families. We aim to develop fact sheets on various topics in the future, and this will be done in partnership with leading professionals in the field and guided by parental involvement. Your thoughts, ideas and suggestions for further development are very much welcomed.
With our warmest regards,
Katy Mitchell (Education Advisor for the Ewing Foundation) and Jennifer Royds (parent of a child with glue ear)
Co-founders of Glue Ear Together
Click here to download a flyer to share with contacts
