Added: 2 years ago
From: DrMoshirfar
Views: 6,638
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  • I noticed problems with my vision when I was 16, but I didn't find out I had this disease till I was 20. I am 24 now, and I have tried all the contacts there are, the small hard ones, I even wore soft lens under the hard ones, now I'm wearing the hybrid gas lens which are starting to become useless. I never really had a job and I still can't get one but I'm in school. It's ashame that keratoconus patients can't get disability, but I will definitely look into the tactic procedure. It looks more

  • I've had this condition for the past 5 or 6 years at the advanced stage now but I haven't let it stop my passions of music (See my channel) and it shouldn't control your life either, stay positive and make adjustments to daily life if you have to!

  • If you are looking for information, support re keratoconus, and

    information on Corneal Cross Linking and other available options,

    please check out this new support page on Facebook called Keratoconus

    Ireland.

  • I do not know what to do I live in Huntsville,Alabama. I do not know what eye doctor who can perform it for me though I have no money due to poverty level at 20K I can either go blind in my right eye or a eye docotor who is willing to help me or any info. thanks

  • I have Keratoconus in my right eye how bad well let's say it is as I read this on my vile container. PWR Minus 14.50 These lens are very expensive a pair is about $500 BCBS of Alabama would not cover it. This is only a temp from getting worse or to say just borrowed time. I am in a poverty level only $20K a year. I had to drop Insurance because it becoming to expensive & despite the fact BCBS would not cover the lens.

  • I have keratoconus, I was diagnosed when Ii was 14 and it was quite advanced. I was made to wear contact lenses from then. I am now 25 and have just been told that they can only adjust the comfort of my lenses and they can no longer do anything to the power (vision) of them.... I am moving to Aussie soon and I hope they are further ahead with their research there than what they are here in NZ.

  • I was diagnosed with Keratoconus at the age of 17, at 18 my eyesight was at least 6x as blury as what they showed in this video. I had cross linking done here in Germany when the procedure just came out, I was one of the first 1000 to get this done. Even though it didn't correct my vision it stopped the Keratoconus disease. I'm now 23 and have been wearing hard contact lenses for about 3 1/2 years, they do bug the shit out of me but get my vision back up to 70-80%.

    CROSS-LINKING RECOMMENDED!!!

  • @naturalBRIDGEonKHWY I am really happy that your vision is better, they really could repair your keratoconus? That is amazing does it mean that you do not have Keratoconus and you can see 20/20 with solely using glasses?

  • This is Iranian accent by the way.

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