The meeting will be open for community members, and we will make an effort to distribute information on ILC in lay language. Arepresentative patient advocate group is working on agenda focused on patients, their families and advocates. We will post updates here. There will be some travel fellowships available. Information will be posted soon.
Selected scientific sessions (based on speakers’ consent) will be recorded and posted on the ILC symposium website after the end of the Symposium (similar to what was done for prior ILC Symposia). It will be available for free, and no registration is required to watch the recorded sessions.