You or someone you know has LCA, RP or some other rare retinal disease. But do you know what your genetic mutation is? Where to go for testing and how you can access free testing? How to work with a genetic counselor? Maybe you know the exact genetic mutation – but do you know what’s next?
Join Sofia Sees Hope founder Laura Manfre and guests Emily Place, Licensed Genetic Counselor at Mass Eye & Ear, and Dr. Brian Mansfield, deputy chief research officer for Foundation Fighting Blindness, live on May 24, and we’ll try to answer all your questions!
Please register for “Know Your Gene: The Importance of Genetic Testing in Inherited Retinal Diseases” on May 24, 2018 2:00 PM EDT at:
After registering, you will receive a confirmation email containing information about joining the webinar.
Brought to you by GoToWebinar®
Webinars Made Easy®