We are creating a Christianson Syndrome database as a way to track the number of cases worldwide. I encourage anyone affected by CS to sign up. Your personal information will not be shared or distributed to anyone outside of CSA. At our 2015 conference, doctors, researchers and clinicians discussed the need to know the number of individuals with CS to better understand and further research.
Why a database?
- Have a known prevalence and track growth rate
- Will assist in applying for government grants and corporate sponsorship
- Will be used to communicate with you any updated research or information that may be of interest.