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Cauda Equina Syndrome Association

Posted , 6 users are following.

Clairecesa
Clairecesa

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.

I hope you'll visit our website and get in touch - we'd love to hear from you image

2 likes, 5 replies

5 Replies

  • kylie46642
    kylie46642 Clairecesa

    Posted

    i would love to know more about this

    • Clairecesa
      Clairecesa kylie46642

      Posted

      Hi KYLIE you can visit our website and click request to join the support group online - you can also join our mailing list - i will keep an eye out for you . you can also ring our helpline

  • eri57096
    eri57096 Clairecesa

    Posted

    Thank you for this!I will definitely visit the website and get in touch!I strongly believe that we can help each other only by exchanging tips on how to deal with CES.

  • emma9138
    emma9138 Clairecesa

    Posted

    Hey, i have been on the website and requested a membership 😃 FANTASTIC IDEA!!!

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