I'm wondering whether the KC group could raise its profile as a campaigning group, or whether the needs of Keratoconus sufferers around the Uk could do with the support of a campaigning group like the RNIB?
Certainly it seems extremely unsatisfactory that so many people with KC seem not to be well supported by the NHS, while folk like myself who live in the general orbit of major teaching hospitals with dedicated cornea clinics enjoy a world class service.
Campaign or mutual support
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Campaign or mutual support
Andrew MacLean
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Campaign or mutual support
How about a 'keratoconus awareness' week? I'm sure most people have never heard of this condition; I certainly hadn't before my son was diagnosed. I didn't know that it was the reason for most of the corneal grafts that take place in the UK (which I read somewhere - probably here!), or appreciate the fact that problems with lenses can mean people have periods when their vision is (temporarily) very poor indeed. Perhaps raising awareness would be of benefit when people with KC need support in education or the workplace?
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To be honest, Anna, that's why I think this site is such a wonderful place.
If we have nudged along imagining that we were alone, or at least part of a small and probably insignificant section of the population, then how can we expect the general public, GP's or even opticians to have any idea of the particular circumstances with which we live?
When we had our recent Scottish group meeting, some folk who had lived with this condition for over twenty years were meeting for the first time other people with the same condition.
I have visited the RNIB site on a number of occasions and they have nothing on Kertoconus. Maybe the first step is to get them to recognize that KC is a not uncommon condition that leads to serious loss of sight and in some cases leaves people legally blind in one or both eyes.
Andrew
If we have nudged along imagining that we were alone, or at least part of a small and probably insignificant section of the population, then how can we expect the general public, GP's or even opticians to have any idea of the particular circumstances with which we live?
When we had our recent Scottish group meeting, some folk who had lived with this condition for over twenty years were meeting for the first time other people with the same condition.
I have visited the RNIB site on a number of occasions and they have nothing on Kertoconus. Maybe the first step is to get them to recognize that KC is a not uncommon condition that leads to serious loss of sight and in some cases leaves people legally blind in one or both eyes.
Andrew
Andrew MacLean
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