Cauda equina syndrome

ClaireCesa
ClaireCesa Community Member Posts: 3 Listener
edited January 2019 in Rare, invisible, & undiagnosed conditions
 I live with cauda equina syndrome I just wondered how many people on here do too? I have had it for 8 years now and would like to connect with others who have been through the same thing

Comments

  • steve51
    steve51 Community Member Posts: 7,121 Championing
    Hi @ClaireCesa

    Welcome it’s my meet you this evening ???????

    I have managed to find you another member who has got the same condition as you.

    Hi @zoe78

    I hope that you can help me with this new member????

    @steve51
  • ClaireCesa
    ClaireCesa Community Member Posts: 3 Listener
    Of course - how?
  • Pippa_Alumni
    Pippa_Alumni Scope alumni Posts: 5,761 Championing
    Hi @ClaireCesa, and a warm welcome to the community!

    I've had a search around and found that @Paul59, @lillian, @salwil89, @K_9 and @Loubell have all spoken about Cauda Equina Syndrome before here on the community. Hopefully they'll be able to get in touch with you here! 
  • mrsp2970
    mrsp2970 Community Member Posts: 2 Listener
    Hi @ClaireCesa
    I had an emergency operation in the year 2000 for having Cauda Equina. I’ve been fine ever since, apart from bouts of excruciating lower back pain. What’s your story? X
  • Chloe_Alumni
    Chloe_Alumni Scope alumni Posts: 10,505 Championing
    Welcome to the community @mrsp2970! :)

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