CXL Club
Posted: Sun 28 Dec 2008 4:52 pm
Hi Everyone
I was talking to a patient one day who was just going through Cross Linking. Although I could give her some idea of what to expect, she was really frustrated saying that she wished she could speak to someone who had gone through it as well. I have also seen a lot of these sort of requests on these boards and I have felt for some time that there is a need for an information site with associated forum so that CXL can be dealt with in more detail from a patient perspective.
I have now created a site and message board (just put up today) for this purpose but although I have created it, I really want input from you yourselves. At least I can see what I am doing to create it but the idea is that anyone who wants to can contribute. So, any links to info about CXL, latest research, information as to where it is being done (both in the UK and abroad) etc etc. As many who have CXL also have intacs it can be about them too.
The message board is the same format as this one and I have asked on the phpbb boards for help in designing a style that is easy to see. It is hoped that between this board and the CXL Club one we will get a couple of styles that are much better for those with poor vision to actually see.
The links are:
Site: http://www.cxlclub.lwvc.co.uk
phpbb thread: http://www.phpbb.com/community/viewtopic.php?f=74&t=1371095
Test board: http://hi.daffie.me.uk/viewtopic.php?f=2&t=2&p=7#p7
If you want to contribute anything like your personal story or any useful links or articles, please email me at my email address in my signature.
Lynn
I was talking to a patient one day who was just going through Cross Linking. Although I could give her some idea of what to expect, she was really frustrated saying that she wished she could speak to someone who had gone through it as well. I have also seen a lot of these sort of requests on these boards and I have felt for some time that there is a need for an information site with associated forum so that CXL can be dealt with in more detail from a patient perspective.
I have now created a site and message board (just put up today) for this purpose but although I have created it, I really want input from you yourselves. At least I can see what I am doing to create it but the idea is that anyone who wants to can contribute. So, any links to info about CXL, latest research, information as to where it is being done (both in the UK and abroad) etc etc. As many who have CXL also have intacs it can be about them too.
The message board is the same format as this one and I have asked on the phpbb boards for help in designing a style that is easy to see. It is hoped that between this board and the CXL Club one we will get a couple of styles that are much better for those with poor vision to actually see.
The links are:
Site: http://www.cxlclub.lwvc.co.uk
phpbb thread: http://www.phpbb.com/community/viewtopic.php?f=74&t=1371095
Test board: http://hi.daffie.me.uk/viewtopic.php?f=2&t=2&p=7#p7
If you want to contribute anything like your personal story or any useful links or articles, please email me at my email address in my signature.
Lynn