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What is Keratoconus?
- Importance of Early Detection
What is Cross-Linking?
- iLink^® FDA-Approved Cross-Linking
Insurance information
- Cross-Linking & Insurance Guide
- Copay Savings Program
Patient Resources
Find an Expert

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What is Keratoconus?
- Importance of Early Detection
What is Cross-Linking?
- iLink^® FDA-Approved Cross-Linking
Insurance information
- Cross-Linking & Insurance Guide
- Copay Savings Program
Patient Resources
Find an Expert

Pamela Disanto

Is Keratoconus Hereditary? A Mother’s Perspective

December 7, 2021July 11, 2018 by Pamela Disanto

Categories Blog, Pamela Disanto

Recent Posts

Keratoconus Journey: Karolyn
Santa Barbara News-Press: Surgical Specialist Performs FDA-Approved Treatment for Progressive Keratoconus
Deseret News: He Has a Rare Eye Disease That Threatens His Eyesight. Now, He Wants to Be an Air Force Pilot
How to Tackle Allergy Season!
Keratoconus Journey: Andrew

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Recent Posts

Introducing the iLink^® Copay Savings Program

Feb 24, 2022

Are you or a loved one living with progressive keratoconus and currently considering your potential treatment options? If your doctor has recommended iLink® FDA-approved corneal cross-linking— the first and only FDA-approved therapeutic treatment that stiffens the...

Keratoconus Journey: Karolyn

Jul 27, 2022

Working as an emergency room nurse, Karolyn is accustomed to evaluating and treating a wide range of illnesses and injuries. However, when she began to experience blurry and worsening vision that made it difficult to drive and see at a distance, Karolyn found herself...

Santa Barbara News-Press: Surgical Specialist Performs FDA-Approved Treatment for Progressive Keratoconus

Jul 20, 2022

“The [iLinkⓇ cross-linking] procedure is FDA-approved, and there is broad commercial insurance coverage for the procedure. It is important to diagnose keratoconus early (starting at late teens) and receive treatment if progression is noted as soon as possible”...

Deseret News: He Has a Rare Eye Disease That Threatens His Eyesight. Now, He Wants to Be an Air Force Pilot

Jul 11, 2022

Derek always wanted to be a pilot in the armed forces and joined the ROTC to help secure a position in the Air Force. However, his dream seemed to be in jeopardy when he learned that he was living with progressive keratoconus during his flight certification. This...

How to Tackle Allergy Season!

Jul 6, 2022

We’re all excited to head outdoors after a cold winter and rainy spring. However, for the millions of people who suffer from seasonal allergies, spending time outside can bring challenges. And, as you may already know, no allergy season is ever the same. A team of...

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© 2022 Living with Keratoconus. Glaukos^® is a registered trademark of Glaukos Corporation. iLink^® is a trademark of Glaukos Corporation. Photrexa^®, Photrexa^® Viscous, and the KXL^® system are registered trademarks of Avedro, a Glaukos company. All Rights Reserved. Glaukos Corporation.

IMPORTANT SAFETY INFORMATION

APPROVED USES
Photrexa^® Viscous (riboflavin 5’-phosphate in 20% dextran ophthalmic solution) and Photrexa^® (riboflavin 5’-phosphate ophthalmic solution) are used with the KXL^® System in corneal cross-linking to treat eyes in which the cornea, the clear dome shaped surface that covers the front of the eye, has been weakened from the progression of the disease keratoconus or following refractive surgery, a method for correcting or improving your vision.

Tell your healthcare provider if you are pregnant or plan to become pregnant.

IMPORTANT SAFETY INFORMATION
Ulcerative keratitis, a potentially serious eye infection, can occur. Your doctor should monitor defects in the outermost corneal layer of the eye for resolution.

The most common ocular side effect is haze. Other ocular side effects include inflammation, fine white lines, dry eye, disruption of surface cells, eye pain, light sensitivity, reduced sharpness of vision, and blurred vision. The risk information provided here is not comprehensive. To learn more, talk to your healthcare provider.

Go to Prescribing Info to obtain the FDA-approved product labeling.

You are encouraged to report all side effects to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.