Keratoconus from Charlotte's perspective

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

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Charlottes mum
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Keratoconus: No, I don't suffer from KC
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Keratoconus from Charlotte's perspective

Postby Charlottes mum » Sat 06 Mar 2010 12:25 pm

"Promise me you'll always remember that you're braver than you believe, you are stronger than you seem and smarter than you think" .....Winnie the Pooh

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space_cadet
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Keratoconus: Yes, I have KC
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Re: Keratoconus from Charlotte's perspective

Postby space_cadet » Sat 06 Mar 2010 4:54 pm

:D :D :D

Awesome and inspiring.

I went to press 'like' then realised I am not on Facebook :p

Great pronunciation as well :)

What a star, have cirulated to friends the link (hope that was ok) x
May09 Diagnosed with KC, March 2010 after a failed transplant it has left me legally blind a long cane user (since 2010) who is blind in a once sighted world

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Andrew MacLean
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Re: Keratoconus from Charlotte's perspective

Postby Andrew MacLean » Sat 06 Mar 2010 5:57 pm

Well done Charlotte

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kitty kat
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Re: Keratoconus from Charlotte's perspective

Postby kitty kat » Sun 07 Mar 2010 1:25 pm

Thumbs up Charlotte xx


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