A voice for those affected by Cauda Equina Syndrome in the UK
We are pleased to be working with the
Spinal Injuries Association to support our members
Our mission is to prevent Cauda Equina Syndrome by raising awareness of the disability across the UK and make the condition a household name by 2022.
Sometimes you just need someone to talk to. Become a member for free and join our forums to link with CES sufferers.
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Whether you have been recently diagnosed or are doing further research, find out more about Red Flag Symptoms and what support is available in the UK
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Our mission is to raise awareness of Cauda Equina Syndrome in healthcare organisations. View and request our literature here.
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‘Bringing together people affected by Cauda Equina Syndrome’
The Cauda Equina Syndrome UK Charity provides support, education and practical advice to individuals affected by CES and their families, and heath care professionals (HCPs) in the UK.
Our aims
Our vision is that everyone diagnosed with CES has access to quality information, informed advice and the appropriate level of support.
Keep up to date with the latest CES news and events across the UK.
Catherine recently emailed us with her CES story for our next instalment of our awareness campaign. Read her experiences here in her own words, is it a similar story to what you or someone you know has been through?
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Next up for our CES awareness campaign is Katrina's story. Katrina contacted us via Facebook, keen to share her experience to help raise awareness. Her story goes to show that no matter how fit you are CES can affect you.
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This month's story has been submitted by Kerry. Read on as she explains her experience of Cauda Equina Syndrome, perhaps you have been through similar?
Read More“The first step towards change is awareness. The second is acceptance.”
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