People with KC in North East

[domenicminniti]

Hi

My sister has KC and is really struggling with things and having a hard time adapting to life with it. Is there anyone based in the North East (we are in teeside) who would be able to meet up to help her with things? Is there a group or something?

Is there another forum that is a little more active than this one? The last post in the most local regional forum was 2007 or something.

Thanks for any help!

Dom

[Anne Klepacz]

Hi Dom and welcome,
I'm afraid we don't have a regional group in the North East, though we certainly have members in that area so maybe you'll get a response from someone near you. And you and your sister can talk to lots of people via this forum - just ask away!
You'll also find some useful leaflets you can download on the home page of this site
www.keratoconus-group.org.uk/sitev3/publications.html
And if you e-mail your postal address to anne@keratoconus-group.org.uk there's other information we can send you (information booklet about the condition, a conference DVD, recent newsletters).
Anne