Keratoconus

bootybouncer

tashiusclay wrote: »

Good luck with it, looking forward to seeing how the SimLc goes for you. Any idea what type lenses you will be offered?

Was in the eye clinic last Wednesday the same as your self....getting sim lc in the right eye in april, and in for fitting next week for a contact lense in the left eye........................ im away for a while in march so i cannot get operation until april................no operation needed in the left eye as yet, but they will monitor it............................it will be money well spent I think

Lads are the contact lenses working out pricey???????? ive heard mad prices quoted for some

MarcusFenix

bootybouncer wrote: »

Was in the eye clinic last Wednesday the same as your self....getting sim lc in the right eye in april, and in for fitting next week for a contact lense in the left eye........................ im away for a while in march so i cannot get operation until april................no operation needed in the left eye as yet, but they will monitor it............................it will be money well spent I think

Lads are the contact lenses working out pricey???????? ive heard mad prices quoted for some

Lenses aren't too bad, around €300 for the pair.

I reckon all the eye drops and Quattro will add up though, 12 euro a bottle and I always keep a backup of both

bootybouncer

MarcusFenix wrote: »

Lenses aren't too bad, around €300 for the pair.

I reckon all the eye drops and Quattro will add up though, 12 euro a bottle and I always keep a backup of both

Thanks champ.......suppose it depends on the lenses that are gonna be fitted ???.......ah next week will reveal all

MarcusFenix

bootybouncer wrote: »

Thanks champ.......suppose it depends on the lenses that are gonna be fitted ???.......ah next week will reveal all

I think so, Clare said that if these didn't fit that the next ones she had to try were like 3000!!! Dunno if that's the pair but its not happening !

bootybouncer

MarcusFenix wrote: »

I think so, Clare said that if these didn't fit that the next ones she had to try were like 3000!!! Dunno if that's the pair but its not happening !

Wow thats crazy, sure the surgerys is pricey enough..........................cracking looking isnt she

MarcusFenix

bootybouncer wrote: »

Wow thats crazy, sure the surgerys is pricey enough..........................cracking looking isnt she

One of the best I've seen! Even before my eyes went to ****

bootybouncer

bump bump

Moldol

i attend eyecatchers opticians in waterford with brian o sullivan and find him very good. i too have spent a small fortune on contacts as i constantly loose or mix them up! im now wearing soft contacts under the hard ones more exspense i wonder if we would be enttled to claim any of the money back as its an ongoing condition

murrayp4

Am I the only one who thinks "Kerry Katona" every time I see this thread??

bootybouncer

bump chappers..................................any updates

Thelostcountry

Bump!

bootybouncer

Thelostcountry wrote: »

Bump!

bump............got cross linking a few days ago

Thelostcountry

bootybouncer wrote: »

bump............got cross linking a few days ago

Hi, how was it? How you feeling post op?

glineli

bootybouncer wrote: »

bump............got cross linking a few days ago

Where did you get it done? how you getting on?

I am getting CK next Monday and CXL next Tuesday on my right eye, again with Dr Cummings. Looking forward to the difference already

bootybouncer

glineli wrote: »

Where did you get it done? how you getting on?

I am getting CK next Monday and CXL next Tuesday on my right eye, again with Dr Cummings. Looking forward to the difference already

Dr Corkin did me, very nice man.......................... scleral lense in the left at the mo, month or six weeks before i can get the right measured, got cxl with bit of laser, simlc...........quite cloudy now and worse than before, but I was told to expect that

whats ck?

glineli

bootybouncer wrote: »

whats ck?

CK is Conductive Keratoplasty.

http://www.allaboutvision.com/visionsurgery/ck_ltk_eye_surgery.htm

I then have CXL 24 hours later. Dr Cummings believes the new shape from CK should be locked down as soon as possible using CXL

bootybouncer

glineli wrote: »

CK is Conductive Keratoplasty.

http://www.allaboutvision.com/visionsurgery/ck_ltk_eye_surgery.htm

I then have CXL 24 hours later. Dr Cummings believes the new shape from CK should be locked down as soon as possible using CXL

Great champ, hope it goes well

ClothesBeam!

Hello there, new here and only recently got diagnosed with Keratoconus about 3 weeks ago.

Went into Specsavers cause of the 15 euro eye test and got sent to Dr Condon afterwards. According to him I've about 10% vision left in my right eye but its only barely starting to take effect in my left eye. He also got in contact with the Mater for me and I'm just waiting to hear back from them to see where i go from here. Have to say, Condon is a pretty great guy, very glad he is here in Waterford.

So since this is all very new to me i have a few questions I'm hoping some of you fine people can help me with

I'm 22 so what i can expect in the years to come?

Like many in Waterford I'm unemployed and on a medical card, will i be covered on the card for treatments? and if not what expenses will come up?

Crosslinking seems to be what I'll need next so whats it like?

And how am i gonna manage getting all these things done to my eyes when i can barely put in the drops without squirming like a freak haha

Thanks for any help you can offer

tashiusclay

Well folks another quick update, following my Cxl in my right eye, and nothing being able to be done with my left eye as its far too thin, I collected my rgp's from Clare in the Wellington on Wednesday, they're only the first pair I've being given, as usually a few trial and error refits are required before a comfortable fit is usually achieved, and these pair aren't fitting as good as they could be, Clare has a slightly modified pair ordered for me which I should have out in the post next week.

But I have to say they are still pretty ok to wear, I'm only breaking them in day by day yet, but I'm quite happy with them, excellent vision from them, more or less 20/20. Strangely, the vision from my bad left eye is even better with the lens than the good right eye with a lens.

The Halo effect at night seems to have improved too, though I'll report better on that when I have them in again tomorrow night and I'll try and get out in the car for a spin.

The lenses I have are No.7 Laboratories SoClear 14mm rgps, well happy with them so far anyway, even on the steep left eye and not fitting as good as they should, they're still very managable. A better fit with the next lenses should make them better again all going well.

tashiusclay

ClothesBeam! wrote: »

Hello there, new here and only recently got diagnosed with Keratoconus about 3 weeks ago.

Went into Specsavers cause of the 15 euro eye test and got sent to Dr Condon afterwards. According to him I've about 10% vision left in my right eye but its only barely starting to take effect in my left eye. He also got in contact with the Mater for me and I'm just waiting to hear back from them to see where i go from here. Have to say, Condon is a pretty great guy, very glad he is here in Waterford.

So since this is all very new to me i have a few questions I'm hoping some of you fine people can help me with

I'm 22 so what i can expect in the years to come?

Like many in Waterford I'm unemployed and on a medical card, will i be covered on the card for treatments? and if not what expenses will come up?

Crosslinking seems to be what I'll need next so whats it like?

And how am i gonna manage getting all these things done to my eyes when i can barely put in the drops without squirming like a freak haha

Thanks for any help you can offer

Try and get the crosslinking done in the good left asap anyway, thats your main priority at the min, hopefully Dr Condon can get this pushed through quickly for you via the medical card through the Mater/Eye and Ear hospital. The crosslinking should be covered on the medical card, I had to go privately as my remaining good eye was already pretty advanced by the time I found out I had Kc, I was too afraid to wait any longer for the Hse to do it for me.

You'll get used to poking and pawing your eyeballs don't worry, I used to hate putting drops etc anywhere my eyes, now its starting to become second nature

tashiusclay

glineli wrote: »

Where did you get it done? how you getting on?

I am getting CK next Monday and CXL next Tuesday on my right eye, again with Dr Cummings. Looking forward to the difference already

Hows the CK'd left eye doing?

glineli

tashiusclay wrote: »

Hows the CK'd left eye doing?

Going great. Its a massive difference. No more squinting. Really looking forward to tomorrow.

Corvo

It's October now since I had the cross linking on my left eye. Thankfully they let me wear soft lens in my good right eye and what a difference comfort wise that it. Even the rigid left one is now better fitted and never slips out or causes itchy red eyes.

Went to Old Trafford last week and really noticed how good my vision now is. AT matches before I would squint and generally feel like I was watching the game on a fuzzy telly.

glineli

Hi all. I had the right eye done with ck on monday and cxl yesterday. Tough going but only for 24 hours. I can see a big difference already. Drive down from dublin was hell though.

glineli

Doing really well after the CK and CXL. Eyesight improvement is unreal. Delighted with it

bootybouncer

glineli wrote: »

Doing really well after the CK and CXL. Eyesight improvement is unreal. Delighted with it

really????????// i got cxl on right eye with a bit of laser.......still cannot see a thing

glineli

bootybouncer wrote: »

really????????// i got cxl on right eye with a bit of laser.......still cannot see a thing

Thats strange. The first 24 hours were rough but from then on it has got better and better. i was having plenty of glare the first few days but that has decreased and now it is great.

Sorry to hear about your experience

bootybouncer

glineli wrote: »

Thats strange. The first 24 hours were rough but from then on it has got better and better. i was having plenty of glare the first few days but that has decreased and now it is great.

Sorry to hear about your experience

what lenses are you using champ???

glineli

bootybouncer wrote: »

what lenses are you using champ???

Not using any lenses. Claire is very surprised that the CK and CXL has improved my vision this much.

bootybouncer

glineli wrote: »

Not using any lenses. Claire is very surprised that the CK and CXL has improved my vision this much.

jesus lucky you champ..................... i cant get a lense on my left until start of May.........Did you get laser with cross linking ????

glineli

bootybouncer wrote: »

jesus lucky you champ..................... i cant get a lense on my left until start of May.........Did you get laser with cross linking ????

I didnt qualify for laser as my cornea is too thin. Dr Cummings just said no to that from the word go. The improvement is due to the CK which reshapes the cornea. As that was taking place i could see the improvment while going out to the other room for new mappings to be taken.

bootybouncer

glineli wrote: »

I didnt qualify for laser as my cornea is too thin. Dr Cummings just said no to that from the word go. The improvement is due to the CK which reshapes the cornea. As that was taking place i could see the improvment while going out to the other room for new mappings to be taken.

I had Dr Corkin........................jesus I hope he hasnt blinded me

glineli

bootybouncer wrote: »

I had Dr Corkin........................jesus I hope he hasnt blinded me

Haha i heard good things about him aswell.

bootybouncer

glineli wrote: »

Haha i heard good things about him aswell.

Hes cool......tbh I was told to expect it to be worse at first for a few weeks, tis a slow process for me.......................maybe mine is worse that yours in the first place...................congrats dude though you must be well chuffed

glineli

bootybouncer wrote: »

Hes cool......tbh I was told to expect it to be worse at first for a few weeks, tis a slow process for me.......................maybe mine is worse that yours in the first place...................congrats dude though you must be well chuffed

Its great alright. My left eye was very bad and I had that done last november. So i was happy to get the right one done as soon as possible.

Hopefully yours will sort itself out.

I did find the procedure tough going though.

bootybouncer

:mad:

glineli wrote: »

Its great alright. My left eye was very bad and I had that done last november. So i was happy to get the right one done as soon as possible.

Hopefully yours will sort itself out.

I did find the procedure tough going though.

Me too pal....................I didnt get much sympathy at home either.........I think people dont see the surgery as such a big deal :cool:

irishproduce

ClothesBeam! wrote: »

Hello there, new here and only recently got diagnosed with Keratoconus about 3 weeks ago.

Went into Specsavers cause of the 15 euro eye test and got sent to Dr Condon afterwards. According to him I've about 10% vision left in my right eye but its only barely starting to take effect in my left eye. He also got in contact with the Mater for me and I'm just waiting to hear back from them to see where i go from here. Have to say, Condon is a pretty great guy, very glad he is here in Waterford.

So since this is all very new to me i have a few questions I'm hoping some of you fine people can help me with

I'm 22 so what i can expect in the years to come?

Like many in Waterford I'm unemployed and on a medical card, will i be covered on the card for treatments? and if not what expenses will come up?

Crosslinking seems to be what I'll need next so whats it like?

And how am i gonna manage getting all these things done to my eyes when i can barely put in the drops without squirming like a freak haha

Thanks for any help you can offer

Hi CB,

Your story is almost identical to mine.
I was about 21 when diagnosed, right eye was shot and had very little useful vision in it. I went straight for graft at the time, just a decision I took myself. That was in 2005. I still have that graft, I had two further corrective surgeries in it in 2012 to release some stretching pressure that was stopping a contact lens from sitting on it (Imagine the contact lens has to sit on a nice round cornea and your isn't round) and since then, the lens I use is called Synergise or Synergeyes or something like that. Its hard and soft in differenth places. Works a treat, use it for hurling and can see pretty much perfect.

My left eye has been getting a little dodgy but at a very slow pace.
I seen William Power in blackrock privately last year and he said there was no need to any treatment on left eye and possibly may never need it as KC generally stops by mid thirties anyway so hopefully that will hold true.

Some points to note from experience.
Because you, like me, have it bad in one eye and not in the other, you are going to gradually notice poor depth perception. If you play sports then this will bother you as the ball may be travelling faster than you perceive or may be slightly at a different distance or angle than you are imagining. If you get some lenses in, it will fix this but after years of managing and adjusting, you will start to feel dizzy :-0

Read some of these facts here:
http://www.scribd.com/doc/91315/7-Vital-Facts-About-Keratoconus-Treatment

Most importantly, you won't go blind, it shouldn't deteriorate forever and technology is advancing all the time. There are already lots of treatments with more coming.

Best of luck!
irish

S.M.B.

I spent an entire day in Moorfields Eye Hospital in London yesterday getting a bespoke scleral lens manufactured that might be an improvement on my current one.

A mould of my eye was taken and within 3 hours I had a perspex version which I could use to check how well it cleared the cornea. Looked like it had the perfect minimal clearance without and glaring points of contact.

Now I have to wait for a proper RGP version to be made to the same spec.

Cost of process & lens in a private lens manufacturing centre in the states: ~ £5,000.
Cost of process & lens in Moorfields with the assistance of the NHS: £54.70.

irishproduce

S.M.B. wrote: »

I spent an entire day in Moorfields Eye Hospital in London yesterday getting a bespoke scleral lens manufactured that might be an improvement on my current one.

A mould of my eye was taken and within 3 hours I had a perspex version which I could use to check how well it cleared the cornea. Looked like it had the perfect minimal clearance without and glaring points of contact.

Now I have to wait for a proper RGP version to be made to the same spec.

Cost of process & lens in a private lens manufacturing centre in the states: ~ £5,000.
Cost of process & lens in Moorfields with the assistance of the NHS: £54.70.

You a UK citizen?

S.M.B.

irishproduce wrote: »

You a UK citizen?

Citizen, no. Resident, yes.

A big reason why I moved over here a few years ago was so that I would be within a short commute of Moorfields Eye Hospital.

The contact lens purchase scheme is just a fantastic benefit to have.

KwackerJack

Hi all

Like many here, after a simple eye examination at Spec-savers and a consultation with a specialist i was diagnosed with KC.

I have be refereed to the Wellington Eye Clinic in Sandyford.


I am 28 and have noticed the past year or so that my left eye was out of focus and my right eye is gradually getting worse also!

I drive a good bit and my work involves computers so its not a good combination for my condition. I also fly and drive a motorbike so I am hoping to have this sorted as soon as I can.

Has anyone any experience of the above clinic?

Thanks

glineli

Welcome KwackerJack

I was just up there yesterday for my 6 month left cxl check up and 1 month right cxl check up. All going well and meeting Claire in July for my contact fitting.

Dr Cummings is excellent. I had CK and CXL on both eyes and it has made a massive difference. The only problem i have is everything is so bright but i can live with that

KwackerJack

glineli wrote: »

Welcome KwackerJack

I was just up there yesterday for my 6 month left cxl check up and 1 month right cxl check up. All going well and meeting Claire in July for my contact fitting.

Dr Cummings is excellent. I had CK and CXL on both eyes and it has made a massive difference. The only problem i have is everything is so bright but i can live with that

Is the brightness a side affect or is that how the eye should be??

What is the approx cost for each eye? I understand it differs from patient to patient patient!

I am going to book a consultation soon then try get time off work

glineli

KwackerJack wrote: »

Is the brightness a side affect or is that how the eye should be??

What is the approx cost for each eye? I understand it differs from patient to patient patient!

I am going to book a consultation soon then try get time off work

The brightness is as expected, the glare would be a side effect of KC.

it cost roughly 2500 per eye. Aviva cover some of the cost of the CXL part, the only insurer in Ireland to do so.

I was off work a week after each eye. The 2 procedures were done within 24 hours of eachother.

MarcusFenix

Hey, I have limited experience with Dr. Cummings or Dr. Corker as I had CXL done in my right eye publicly before going to see them and so was referred to Clare immediately.

I can't praise her enough for her treatment and attention to detail. If you do end up with her for lenses you won't be disappointed.

glineli

MarcusFenix wrote: »

I can't praise her enough for her treatment and attention to detail. If you do end up with her for lenses you won't be disappointed.

Going to see Claire first week in July. Hopefully i can get away with the soft contacts.

Corvo

Claire is hot by the way

:pac:

KwackerJack

Corvo wrote: »

Claire is hot by the way

:pac:

Excellent

Looks like its time to start saving, 1500 minimum per eye is expensive but its my eyesight so its worth it

bootybouncer

shes married fellow blind chaps

KwackerJack

bootybouncer wrote: »

shes married fellow blind chaps

AND Not implying anything!!

Anyway I'm going for light treatment and maybe pills / injections for my psoriasis. Does anyone off hand if any of this affect KC or the CCL procedure??