UK Keratoconus Self-Help and Support Association

Hello KC friends, My daughter is 20 and a KC suffer. She’s amazing and very strong. Since she was diagnosed at 16 I have been constantly scared for her and her future. It’s a horrible feeling and unless your living it people don’t understand. So I am reaching out to other parents and sufferers. Mayb...

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 on a daily basis. I have wanted to post Brooke‘s experiences so often but it never felt right. Now I want to tell her story and hopefully it can resonate with other ...