After Treatment with LUXTURNA, It’s a New Year, New Vision
Two little girls – one on the East Coast and one on the West Coast – ring in this New...
Family Stories
Living with LCA: ‘It does no good to have pity’
Mikayla Larson, a 30-year-old mother living with a rare inherited retinal disease (IRD) called Leber congenital amaurosis (LCA) wants to reassure children living with...
‘As A Doctor, You Will Never Forget’
Transforming laboratory research into real-life therapy for patients is a rare occurrence. But when it does happen, it’s big. Huge,...
Tell Us Your Story: ‘Do Not Limit Yourself’
I am 22 years old and I have LCA. My name is Angélica Bretón Morán, I am from Mexico, I...
An Amazing Year
This is the seventh in a series following the progress of Creed Pettit, a 9-year-old Florida third-grader, who completed treatment...
Living With LCA: Maverick Johnston
A revolutionary genetic treatment could improve the vision of 5-year-old Maverick Johnston, but his mom first wants to know more...
Life After LUXTURNA: ‘Now He Can See’
This is the sixth in a series following the progress of Creed Pettit, a 9-year-old Florida third-grader, who completed treatment...
College Connection: Making A Successful Transition To College
Starting high school or going off to college is not easy; new people, classes and sometimes even a new city...
His Future’s So Bright, He’s Gotta Wear Shades
This is the fifth in a series following the progress of Creed Pettit, a 9-year-old Florida third-grader, who completed treatment...
Post-Surgery: Beginning to See the Light
This is the fourth in a series following the progress of Creed Pettit, a 9-year-old Florida third-grader, who completed treatment...