My Nonprofit Reviews

I knew nothing about keratoconus (KC) when I was diagnosed. I was frightened and worried about my future. When I found NKCF online, it was such a relief. I was not alone! There were doctors who were ecperienced with this condition; there were patients like myself who really, truly knew what I was going through. It was a tremendous support. Their day-long seminar at the Skirball was very informative, and a chance to meet other KC patients in person. When it came time for my first cornea transplant, NKCF was there, too. Their booklet about cornea transplants was extremely helpful in my planning and knowing what to expect. And it was free! Although my transplanted corneas are healthy now, I still visit the NKCF and support them with my participation on the chat board and monetary donation. This organization is suberb, and has made a huge difference in my life with KC!

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