Stand With Aaron for CES Awareness
In August 2012, I was diagnosed with a rare, serious neurological and musculoskeletal disorder called Cauda Equina Syndrome (CES). After starting to research CES on the internet, I found a sort of black hole of knowledge about the disease. Though this is starting to improve, through websites, support forums, and social media pages on Facebook and Twitter, I wanted to provide a sort of repository of scientific research and educational tools. My goal is to make my site accessible and relevant to anyone, especially those living with CES, their families, friends, and caregivers.
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