Cauda Equina and pregnancy

Louise shares her story with us about pregnancy after CES. Read more

A Mothers story...

A Mother shares her story with us on how CES has impacted her life forever. Read more

Our story

In August last year we were thrilled to finally achieve national coverage of cauda equina syndrome in the media. Read more

Dedicated CES pathways

Claire Thornber explains why dedicated care pathways and post operative services are so important for cauda equina syndrome patients. Read more

A tale of two sisters !

Jo and Liz are two sisters whose lives and relationship has been forever changed by CES. Read their story... Read more

Paul's story - Returning to work

Paul shares with us his inspiring story about returning to work after delayed diagnosis of cauda equina syndrome. Read more

Tegan's story - Living with a parent with a disability

Tegan is 15 years old, when she was 13 her Mum was diagnosed with Cauda Equina Syndrome. Tegan tells her story on what it's like living with a parent with a disability and offers advice to other children in the same situation. Read more

Who is up for the challenge??

Our first fundraiser of 2022 running from 1st March 2022 to 1st October 2022. - Moneys raised will provide vital funds for our dedicated therapy and wellbeing courses. - Who is up for the challenge?? Read more


We are extremely proud to announce our new connect service. CES BUDDY! - We have 11 lovely volunteer CES Buddies who will be there to offer telephone support to anyone who may feel isolated and are struggling with the daily CES battles. Read more