
Having KC is not disastrous!
I am now 80 and was diagnosed with KC in 1978. Used hard contact lenses from 1965 (not gas permeable in those days) until right

I am now 80 and was diagnosed with KC in 1978. Used hard contact lenses from 1965 (not gas permeable in those days) until right

UPDATE 1st April 2026: After a long and often frustrating journey, I’m incredibly relieved and grateful to say that the NHS contact lens service has

Around the age of 15/16 I was diagnosed with keratoconus. I was a glasses wearer, but I was really struggling to see anything in much

Without and With Lenses Hi I’m Dale, I have Down syndrome, I’m autistic, I can be extremely challenging because the world doesn’t suit me very

“I have had suspicions that you might have Keratoconus in your left eye” In the early 1990s I went to see my optometrist back home

In December 2020 I underwent cross linking at Birmingham Midland Eye Centre. The procedure was on both of my eyes and I had the operation
So I am a parent of a Keratoconus sufferer. Since she was diagnosed at 16 I have struggled to understand what my daughter goes through
A while ago I wrote this, just really to get it off my mind and keep it down to look back on in the future,
I’m 27 and live in edinburgh and was originally told I had KC when I was 12 years old I can remember it well as
I was first diagnosed with KC around 11 years ago, but I really didn’t think that much about it at the time, and it hardly