Cauda Equina Foundation Presents:
3rd Annual Virtual International
Cauda Equina Syndrome Conference
We are happy to be back!
Last year's symposium was a huge success and we are so happy to be back again this year! Thank you to all of our volunteers who make these symposiums happen. We would also like to thank all of our attendees for your active participation, without you this wouldn't be the success that it is.
If you missed our first two symposiums, don't worry- we post all of our educational symposium videos on our YouTube channel. Our patient panel discussions and some of our guest speaker sessions are not posted to respect their right to privacy.
If you missed our first two symposiums, don't worry- we post all of our educational symposium videos on our YouTube channel. Our patient panel discussions and some of our guest speaker sessions are not posted to respect their right to privacy.
Mark your Calendar
Friday, November 3rd, 2023, 7:00 PM EST: Kick-off Party and Patient and Family Meet-Up. Games and Prizes. Join us for our pajama party kicking off Cauda Equina Syndrome (CES) Awareness Month Followed by our 3rd Annual Virtual International Cauda Equina Syndrome Conference!
Saturday, November 4th, 2023, 11:00 AM EST until 5:10 EST: Educational Seminars and Patient Discussion Panels
Sunday, November 5th, 2023, 11:00 AM EST until 4:30 PM EST: Educational Seminars and Patient Discussion Panels
*This is a virtual event. All times posted are in Eastern Standard Time (EST).*
Saturday, November 4th, 2023, 11:00 AM EST until 5:10 EST: Educational Seminars and Patient Discussion Panels
Sunday, November 5th, 2023, 11:00 AM EST until 4:30 PM EST: Educational Seminars and Patient Discussion Panels
*This is a virtual event. All times posted are in Eastern Standard Time (EST).*
Meet Our Presenters
Join us on a learning journey through cauda equina syndrome (CES) for our 3rd Annual International Cauda Equina Syndrome Symposium. We bring in experts of the field (many living with CES themselves) to present educational topics on CES to both patients and healthcare providers. This year's focus is on living your best life with CES. Topics will range from how to assemble your care team, self advocacy, long term CES patient monitoring, traveling with CES, and patient panels discussing overcoming stigmas, adjusting to life with chronic CES, and more!
Our symposium, research, and patient support programs are made possible by our generous donors. Please consider donating to support our efforts to improve the quality of life and care for individuals living with cauda equina syndrome.
CES is a complex rare disease, not "Just a Bad Back". *We strongly encourage both patients and their family and friends to attend to better understand the complexities of CES.*
Our symposium, research, and patient support programs are made possible by our generous donors. Please consider donating to support our efforts to improve the quality of life and care for individuals living with cauda equina syndrome.
CES is a complex rare disease, not "Just a Bad Back". *We strongly encourage both patients and their family and friends to attend to better understand the complexities of CES.*
