Claude represents anybody living with Cauda Equina Syndrome (CES).
Claude could be a man or woman, young or old, living anywhere in the world.
Through personal experience, Claude understands the importance of raising awareness of the correct diagnosis and early treatment of CES. Claude has experienced the devastation and isolation and caused by this neurological condition and recognises the importance of being connected and supported by people who’ve been through the same life-changing experience.
Claude’s personal story is a typical one.
Claude tells of delayed diagnosis and treatment, lack of support and of the struggle with acceptance of a life changing condition.
The Cauda Equina Syndrome Association (CESA) is here for people like Claude and their families. To find out more about CES please visit CES Made Simple page.
We aim to embrace people living with CES and by using our collective voice, we hope we will bring about change and an end to unnecessary suffering. The UK has the highest incidence of CES. With the help of our members, we hope to change this and empower and support people to continue to live positive, happy lives.
As a healthcare professional we hope you can help us spread the word, raise awareness and reach patients. We hope you will use our site and services as a valuable resource in your day to day work and that by working together we can really make a difference.
More about the symptoms can be found on our Red Flags section.
To contact the Cauda Equina Syndrome Association email us or phone our helpline 03335 777 113
Cauda Equina Volunteers
We wouldn’t exist without the help of our volunteers. We are very grateful but always looking for more help ! If you live with CES either as a patient or family member and would like to dedicate some of your time to spread awareness and reach patients, we would love to hear from you! We have lots of different roles and need people with all sorts of experience, as well as those just willing to get stuck in. Please complete our volunteer form.