Just want to know every uk KC'ers opinions on what is the only treatment/cure solely for our disease, if your not sure what it is or haven't been told enough go to http://www.kcglobal.org they have reliable information on their website.
Please everybody who reads this vote.
tom
Collagen cross linking (C3r) poll Please Vote!
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- tommy.dean
- Regular contributor
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- Joined: Tue 10 Jan 2006 11:13 am
- Keratoconus: Yes, I have KC
- Vision: Graft(s) and good vision
- Location: Blackburn
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- tommy.dean
- Regular contributor
- Posts: 111
- Joined: Tue 10 Jan 2006 11:13 am
- Keratoconus: Yes, I have KC
- Vision: Graft(s) and good vision
- Location: Blackburn
- Contact:
- Pat A
- Forum Stalwart
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- Joined: Fri 08 Dec 2006 9:42 pm
- Keratoconus: No, I don't suffer from KC
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Tommy
(My personal view!) I understand and sympathise with your frustration - but I won't vote on this issue because I do not feel well enough informed to make a vote that is worth making. There is a lot of information available elsewhere but it is conflicting at times and I believe it is wrong at this stage to expect lay people who are members of this forum to vote on this with anything other than emotion! I suspect like everyone else I want an instant cure for KC (even though I may not have it but we won't go there at the moment!) but there simply is not enough evidence to support the statement that C3R is a cure for KC. But do keep posting - your contributions are very valuable!
(My personal view!) I understand and sympathise with your frustration - but I won't vote on this issue because I do not feel well enough informed to make a vote that is worth making. There is a lot of information available elsewhere but it is conflicting at times and I believe it is wrong at this stage to expect lay people who are members of this forum to vote on this with anything other than emotion! I suspect like everyone else I want an instant cure for KC (even though I may not have it but we won't go there at the moment!) but there simply is not enough evidence to support the statement that C3R is a cure for KC. But do keep posting - your contributions are very valuable!
Pat
We do not stop playing because we grow old;
We grow old because we stop playing.
We do not stop playing because we grow old;
We grow old because we stop playing.
- tommy.dean
- Regular contributor
- Posts: 111
- Joined: Tue 10 Jan 2006 11:13 am
- Keratoconus: Yes, I have KC
- Vision: Graft(s) and good vision
- Location: Blackburn
- Contact:
Hey pat yeah your right about the conflicting information but that's why i posted the kcglobal website along with it. If you go on their wesite you can trust the information.
The KC group could also be like this website but for some reason it chooses to also mis inform.
tom
An alliance of International patients and professionals founded KC Global in 2001 in response to having no information or mis-information about our eye condition, and also due to having no support available to make informed choices.
The KC group could also be like this website but for some reason it chooses to also mis inform.
tom
- Mike Oliver
- Contributor
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- Location: London
- tommy.dean
- Regular contributor
- Posts: 111
- Joined: Tue 10 Jan 2006 11:13 am
- Keratoconus: Yes, I have KC
- Vision: Graft(s) and good vision
- Location: Blackburn
- Contact:
hey mike, that's what i was like in 2003 /04 an after a conversation with then my surgeon i decided not to look into having the treatment. In hind site with what i know now i wouldn't have had to have grafts and wouldn't have spent the next 3-4 years as a severely visually impaired man. 7 years i spent on the nhs struggling with their so called "treatments" for our disease, with low vision. It took 7 months with the right treatment to rehabilitate my vision. But none of this needed to occur and only through being mis guided and being miss informed it did. I want all people who don't have to go through what i have to know all the facts.
tom
tom
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