Keratoconus Awareness

General forum for the UK Keratoconus and self-help group members.

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Clarisa
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Posts: 7
Joined: Sun 30 Oct 2005 12:00 am
Keratoconus: Yes, I have KC
Vision: Contact lenses
Location: Romford

Keratoconus Awareness

Postby Clarisa » Wed 15 Mar 2006 12:40 am

Hello to everyone living with Keratoconus!

Recently I have found it really hard to explain my condition to people, especially when it comes to my lenses (Scleral). I know that there are booklets, leaflets and websites such as this one where people can obtain information but I really feel that there is a need for a documentary that describes Keratoconus. Perhaps one where they follow different people living with Keratoconus at different stages (First diagnosis, wearing new lenses and post op).

I'd appreciate feedback on this
Clarisa

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Knight
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Posts: 188
Joined: Thu 12 May 2005 1:31 pm
Keratoconus: Yes, I have KC
Vision: Graft(s) and contact lenses
Location: classified

Postby Knight » Wed 15 Mar 2006 12:56 am

Although I'm sure this is not entirely what you have in mind, there's a DVD in the works hopefully showing the meetings and conferences:
We talked about it here and there are other links within that thread:
http://www.keratoconus-group.org.uk/for ... php?t=1074

But I like to see something such as a documentary actually too. There's a local film company within the area that I live in called 'New Faces', and I have emailed them as a proposal for a suggestion for maybe a one off - they haven't replied but its early days, also next week I'm sending some stuff to the local newspaper to maybe cover something about KC ... we'll see ...
Only those with KC know the hidden beauty of a Christmas Tree.

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Andrew MacLean
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Keratoconus: Yes, I have KC
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Location: Scotland

Postby Andrew MacLean » Wed 15 Mar 2006 7:46 am

A tv documentary would be a good idea; if you could be sure that they would get it right! A video documentary would make it possible to plug it in and sho folks at home.

I usually resort to the paper and pen method. I draw a picture of the eye and make the cornea kind of pointed. This allows me to explain that what I see is not light focussed ib thge back iof my eye, but scattered painfully about the inside of my eye, giving me both poor sight and some pain!

I sometimes even draw a nice contact lens over the cone to show how much better life is (or in my ase was) when the lens was in place.

Where does this break down? My drawing skills are abismal. :roll:

Image

See what I mean?

Andrew
Andrew MacLean

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Susan Mason
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Posts: 414
Joined: Sat 24 Jan 2004 11:27 pm
Keratoconus: Yes, I have KC
Vision: Contact lenses
Location: Bolton Lancashire

Postby Susan Mason » Sun 19 Mar 2006 12:51 am

Hi Clarisa

Do you think it was difficult to explain your KC to others for a particular reason? What I mean to say is do you think they really listened to what you had to say?
I have had this problem with some people for a long time. They ask what the problem is however, really are not a bit interested and by the time you take your second breath they have switched off. This usually results in a similar conversation being repeated quite frequently and me wanting to stamp on peoples glasses to give them a view of my world.

Maybe everyone should be made to wear scleral lenses for a while and then maybe silly comments such as 'well I wear my contact lenses from 7am in the morning until 11pm at night' :evil: would not be made

If you have KC you are very likely not going to be able to do this. Also as you probably look quite normal to other of course there can't be anything wrong with you can there?

Keep trying, Clarisa is all I can suggest eventually the penny will drop.

best wishes

Susan
don't let the people that mean nothing to you get you down, because in the end they are worth nothing to you, they are just your obstacles in life to trip you up!


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