35 years of KC, and what next…
Posted: Sat 28 Jun 2008 1:25 pm
I was diagnosed with KC in 1973 while I was student. I had my first lenses in Stafford and later moved to West Midland and received treatment in Coventry and Warwick hospital. Up to 5 years ago my job was in software and hence long periods of computer work followed by TV till bed! Then the company I worked for followed the collapse of .com and I decided to go to Israel for voluntary work. Here I am in construction, hence less computers and also I have managed to not have a TV… BBC radio and books do me fine!
In general my KC has not worsened significantly but, due to long periods of using contacts, I am told I have scaring and significant thinning. Last year my right eye became uncomfortable and eventually I was told there is a secondary dimple on the cone that causes the problem. I am now using a piggy-back in the right eye. Not having a TV it means I can take the lenses out when I get home, and to read, I can manage from 15cm – or I squint. However, I have a strong feeling the piggy-back will be short lived and, returning to UK next year, I need to consider the next steps.
Having read the information on this site it looks to me it is unlikely to be recommend for intacs or C3R, which leaves me with cornea graft or Scleral contacts. I e-mailed Sclerals Ltd for information but got no reply.
Does anyone know if this product is still an option, and what is the process, the costs, NHS or not?
In general my KC has not worsened significantly but, due to long periods of using contacts, I am told I have scaring and significant thinning. Last year my right eye became uncomfortable and eventually I was told there is a secondary dimple on the cone that causes the problem. I am now using a piggy-back in the right eye. Not having a TV it means I can take the lenses out when I get home, and to read, I can manage from 15cm – or I squint. However, I have a strong feeling the piggy-back will be short lived and, returning to UK next year, I need to consider the next steps.
Having read the information on this site it looks to me it is unlikely to be recommend for intacs or C3R, which leaves me with cornea graft or Scleral contacts. I e-mailed Sclerals Ltd for information but got no reply.
Does anyone know if this product is still an option, and what is the process, the costs, NHS or not?