• About
    • Our Story
    • Our Vision/Mission
    • Our Team
    • Hope in Focus Ambassadors
    • Pressroom
  • Living with LCA
    • What is LCA?
    • ID Your Gene
    • Clinical Trials
    • Family Connections
  • Community
    • Community News
    • Hope in Focus Podcast
    • Resources
    • Rare Retinal Disease Glossary
  • Events
    • Chef’s Menu at Cedars
    • Holiday Shop
    • Photo Gallery
  • Contact
    • Get in Touch
    • Newsletter
  • DONATE
    Leber Congenital Amaurosis Leber Congenital Amaurosis Leber Congenital Amaurosis Leber Congenital Amaurosis
    • About
      • Our Story
      • Our Vision/Mission
      • Our Team
      • Hope in Focus Ambassadors
      • Pressroom
    • Living with LCA
      • What is LCA?
      • ID Your Gene
      • Clinical Trials
      • Family Connections
    • Community
      • Community News
      • Hope in Focus Podcast
      • Resources
      • Rare Retinal Disease Glossary
    • Events
      • Chef’s Menu at Cedars
      • Holiday Shop
      • Photo Gallery
    • Contact
      • Get in Touch
      • Newsletter
    • DONATE

    Blog

    0
    By Rosanne Smyle
    In Blog
    Posted May 28, 2018

    Parent Support On Line 1

    In the sometimes-isolating world of rare inherited retinal diseases (IRDs) such as Leber congenital amaurosis (LCA), another option exists to help bring people together – support by telephone. [...]

    READ MORE
    0
    By Rosanne Smyle
    In Blog
    Posted May 10, 2018

    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 about the side effects and capabilities of the breakthrough drug [...]

    READ MORE
    0
    By Rosanne Smyle
    In Blog
    Posted April 20, 2018

    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 in March with the breakthrough gene-therapy drug called LUXTURNA™, [...]

    READ MORE
    0
    By Rosanne Smyle
    In Blog
    Posted April 13, 2018

    New Patient Services Program Helps People Navigate Their Road To A Cure

    Now that LUXTURNA™ has come to market as a revolutionary vision-restoring genetic treatment, how does it get to patients? The answer to that question and many others can be found within […]

    READ MORE
    0
    By Sofia Sees Hope
    In Blog
    Posted April 9, 2018

    College Connection: Making A Successful Transition To College

    By Jack McCormick Starting high school or going off to college is not easy; new people, classes and sometimes even a new city makes for a stressful transition. Doing it […]

    READ MORE
    0
    By Rosanne Smyle
    In Blog
    Posted April 7, 2018

    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 in March with the breakthrough gene-therapy drug called LUXTURNA™, [...]

    READ MORE
    0
    By Rosanne Smyle
    In Blog
    Posted March 28, 2018

    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 in March with the breakthrough gene-therapy drug called [...]

    READ MORE
    0
    By Rosanne Smyle
    In Blog
    Posted March 25, 2018

    After Luxturna™ Treatment: ‘Mom, Pop, is that you sitting there?’

    Christian Guardino underwent experimental eye surgery five years ago with a revolutionary genetic treatment called LUXTURNA™, forever changing his life by restoring his vision that was lost due [...]

    READ MORE
    0
    By Rosanne Smyle
    In Blog
    Posted March 19, 2018

    Living Without LCA: ‘Andddddd we’re off”

    “Andddddd we’re off 💓,” Sarah St. Pierre Pettit wrote Saturday afternoon as she, her son, Creed, and her fiancée, Chad, piled into their SUV. They’re headed south for Miami’s Bascom […]

    READ MORE
    0
    By Rosanne Smyle
    In Blog
    Posted March 12, 2018

    Misty Lovelace: ‘I Can See Little Things’

    Told at age 12 she would be blind by 18 because of her Leber congenital amaurosis, Misty Lovelace of Kentucky participated in the gene therapy trials for LUXTURNA, to treat […]

    READ MORE
    1 2 3 4 5 6 7 8 9 ...
    page 1 of 18
    Sign Up for Our Newsletter
    NEWSLETTER SIGN UP
    Get In Touch
    • 860-266-6062
    • info@hopeinfocus.org
    Follow Us
    Hope in Focus is a 501(C)(3). © All rights reserved.
    Please read our Privacy Promise.
    Skip to content
    Open toolbar Accessibility Tools

    Accessibility Tools

    • Increase TextIncrease Text
    • Decrease TextDecrease Text
    • GrayscaleGrayscale
    • High ContrastHigh Contrast
    • Negative ContrastNegative Contrast
    • Light BackgroundLight Background
    • Links UnderlineLinks Underline
    • Readable FontReadable Font
    • Reset Reset
    By continuing to use our website, you acknowledge the use of cookies.