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Hi, I run The Cauda Equina Syndrome Association CIC. We are a patient led non profit, supporting people and raising awareness of CES. I am posting to let you know about our services. We run support group meetings around the UK, a helpline, online support groups and have over 1500 members from around the world. If you have a question or worry, or a tip to help others, you can reach someone who can help you/you can help. We are holding a bank holiday Barbeque on August Bank holiday and run social events where you can meet others face to face.
We ate currently setting up our new charity which will offer residential workshops, training opportunites fund raising events to benefit anyone affected by CES.
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