I was referred to Discovery Eye Foundation's blog by someone who understood that their information would be helpful to me. I have a family member dealing with macular degeneration, and I was just looking for information and people to talk to. Their staff is incredibly compassionate, resourceful, and informative, and I'm greatly appreciative for all of the help they've provided me with!
The Discovery Eye Foundation supports eye research for blinding eye diseases. Its efforts in keratoconus and macular degeneration eye research make the Discovery Eye Foundation a critical component in progressing against these blinding diseases. These innovative research areas include stem cell retinal regeneration, age related macular degeneration genetics, and corneal transplantation and scarring. The Discovery Eye Foundation's work is vitally important to the understanding of the health of the eye. Its website www.discoveryeye.org is a valuable resource for people dealing with eye disease. This is an exceptional organization which deserves the highest praise and support.
The Discovery Eye foundation is unique amongst non-profits in how many people they help in relation to how many people they are. I have rarely seen any organization where their people are so hard working and have such a deeply rooted personal interest in what they do. Truly a stellar organization with stellar individuals!
I have seen DEF grow over the years and they provide a great source of information and comfort for those suffering with eye disease. They sponsor ground-breaking research into the source of many of these aliments and provide patients with support and clear information to help them manage or treat their disease. It's amazing to see such good work produced by their small, but dedicated staff.
I was first referred to Dr. Anthony Nesburn, Medical Director for the DEF, as a result of his expertise, both clinically and in the field of ophthalmic research specific to my medical needs. Continuing as his patient for over forty years, I have been the beneficiary of both his wisdom and compassion. Throughout this time, I've witnessed the unwavering devotion he has demonstrated not only to his own research, but in his support of the research of others through the Foundation.
On a separate note, my family and friends have suffered from the impacts of both AMD and Keratoconus.
The community outreach the Foundation affords those suffering with these serious eye conditions
is so very important.
It has been my privilege to offer financial support for the last several years to an organization accomplishing much in different arenas.
Over the years, 30 to exact, I have watched Discovery Eye Foundation blow the lid off off of so many unsolvable problems! From Keratoconis, to mitochondria genetics, Ocular herpes, Potassium osmosis, and a subject close to my eyeballs, pterigum.
All kidding aside, these researchers are leading scientists who care about everyone.
Do great work. Are starting to produce some very important discoveries that will not only save lives but allow thousands of people such as my father in law to see.
I was a patient of Dr. Anthony Nesburn, when I presented with a challenging corneal problem. His compassion, expertise, conservative approach and overall care were exemplary. I since learned about the foundation he supports, and have been a donor - and passionate fan - ever since, in support of the foundation's good works, Dr. Nesburn's selfless service, and their goals.
In my professional life, I am CEO of a non profit organization - and I've served in similar capacities for over 30 years. The Discovery Eye Foundation is an incredible organization, from all perspectives.
NKCF has helped me gain insight to my son's keratoconus. I rely on it to keep me updated among other sources.
The National Keratoconus Foundation Newsletter has been a hugely helpful resource for us in keeping informed about developments in the study and treatment of Keratoconus.
I was diagnosed with keratoconus over 10 years ago. Every year my condition worsened, and my ophthalmologist did her best to fit me in new contacts each year. It has been a struggle, and I eventually could no longer drive at night at the age of 48. The DEF newsletter helped me be informed about this condition and about the corneal crosslinking (CXL) study. This information was so valuable to me as I knew very little about keratoconus, how it was treated, and the status of the study. Because of my age, I wasn't a candidate for the (CXL) study until last year. I had the procedure completed in both of my eyes 6 months apart from each other. Being part of the study took lots of time, patience, and many appointments; not to mention having to live and not being able to drive without my medically necessary contacts for several weeks before and during recovery. But because I was better informed, I felt confident that the CXL procedure was the right choice for me at that point in my life.