Robert “Bob” Bellizzi 4/13/1931 – 4/8/2024

Executive Director and Founder of The Corneal Dystrophy Foundation

Our mind says that he is no longer in pain but our hearts and family feel the loss. Bob was laughter, love and joy in our family.

Sound Familiar?

“When I was first told I had Fuchs’ Dystrophy I had no idea what it was or what I should do…”

We are here to help.

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The Corneal Dystrophy International Online Support Group

The Fuchs’ Friends international online support group is a place of support and information for people with all types of Corneal Dystrophy.

Patient Story

“I was terrified of going blind.”

After finding an amazing surgeon from Fuchs’ Friends, this patient’s confidence superseded her nerves.

Patient Advocacy & Support thru Fuchs’ Friends®

Since 1998, helping thousands of people in 160 countries to find corneal help, the Corneal Dystrophy Foundation provides support and information for individuals and families with a corneal dystrophy.

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We offer a vast major of services via literature, support groups, and localized specialists.

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Corneal Articles

Research Articles

DMEK, DSO, and Gold Standards

In the title of her article1 published in the journal Cornea in 2022, Dr. Kathryn Colby poses an important question regarding the contemporary and emerging treatment of Fuchs Endothelial Corneal Dystrophy (FECD): “Descemet Stripping ...

Patient Stories

Esta’s Story – Please don’t wait!

I was born with amblyopia left eye and astigmatism, and decades later developed cataracts and floaters. Despite Ophthalmic exams, I went undiagnosed with my vision declining to legally blind in left eye and severe symptoms effecting ...
CDF Patient Stories
CDF BLOG

Corneal Dystrophy Foundation Blog

Why We Smile

Meet Wade:(details are not given to protect his privacy) Monday, Wade’s grandmother emailed the Corneal Dystrophy Foundation. Wade was 5 days old, born in the Midwest.  Wade was diagnosed with CHEDS a major eye problem that could ...

Bob Bellizzi and Dorothy Acton were Godsends when I was diagnosed with Fuchs in the early 2000s and a full corneal transplant was the standard of care.
What a difference Bob made! He was a force of nature, and it is because of him and his legacy, the CDF, that we have so many more options and outstanding surgeons.  We have come from being told that we will go blind if we have Fuchs’ Dystrophy to DSEKs, DMEKs and DSOs.  I worked a couple of conferences with Bob and had many conversations with him when I was facilitating the NoVa/DC/Maryland Local Group.  I would like to say to Monica and the family on behalf of all of us, that Bob will be truly missed, and his legacy and leadership will live on.  Well done, Bob!

Left DSEK, 8-2005, Dr. Price Right DMEK/Triple, 7-2014, Dr. Jun

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