June 29, 2010
When I was first diagnosed with Keratoconus 14 years ago, I've never heard of the disease. My eye doctor gave me the NKCF booklet and I logged onto their website. The newsletters have been very informative and the KC link has served as a helpful resource—many of my questions were answered by people who have experienced my situation. In fact, when I had my transplant 2 years ago, I was able to compare notes with someone who's surgery was days before. We created our own little support group... something that wouldn't have happened without the KC link.
I've personally experienced the results of this organization in...
the wealth of information I have received through the KC link and newsletters.
How frequently have you been involved with the organization?
About every week
When was your last experience with this nonprofit?
MY ROLE:Client Served & Recieved support through the KC link and also a recipient of the NKCF newsletter.