I am 70 years old and have cataracts in both eyes. I initially decided to go with the Restor lens from Alcon - but it's not available. I need 8.5 to 9.0D and I also have some astigmatism (don't know what it is). By now I have been waiting for over a year and my vision gets progressivly worse. I am now using my driving glasses to do close up-work. I don't mind wearing glasse, but could never get used to bifocals. The only thing I am really concerned about is the Depth of Field issue, e.g. I want to be able to see (in focus) my speedometer and the road ahaed of me without having to switch glasses. Any help would be appreciated.
Maybe it would be better if you tried not to use the glasses. I read that for some, it can take 9 months for the brain to adjust to multifocal implants. I gave up on the halos improving after 8 months, and then to my shock, in the 9th month, they are getting smaller. Maybe using glasses is preventing your brain from adapting to the Restor.
I went to another doctor to find out the risks of having the ReStors removed. He wants to get my surgery records and examine me again. I really doubt that I'll have the nerve to go through more surgery though. Something else would go wrong. The fluttering drives me nuts, but it's not all the time, worse with bright fluorescent lights like a grocery store or with reading for too long. At least I CAN see and read. So it could be worse. I'm TERRIFIED of going blind.
I asked this new specialist how the ReStors were supposed to work. He said, frankly, he'd been trying to figure that out for a long time and still had no idea! He does put ReStors in, and I asked him how many he'd taken out. He said none. I asked him how many IOL's of any kind he'd taken out and he said hundreds. Which sounds like a lot, but from his age he's probably been doing this for 30 years, so that's maybe one a month. Though they probably didn't do as many explants until the multifocals were invented. When I see him again I'll ask him how many of the hundreds were successful.
Anyone, I desperately wish I'd never heard of the ReStors!!!!!!!!!
Susan12345
Yes, I know what you mean about terrified. Initially I wanted my lens removed too. But it was too much of a risk for me also. But after many months, my vision came in very clear. You should be able to read without glasses, as that is Restor's strong selling point.
You are obviously a more tolerant person than me when it comes to your vision. There is simply no way I would accept the vision you reportedly have. First, I'd consult other surgeons familiar with ReStor. If they thought laser enhancement would help, I'd do it. Otherwise, I'd have the lenses explanted and replaced with something that would work better for me.
I notice halos, but they are not large and, unless they are halogen (those very white headlights), they don't bother me. I don't do much night driving anyway.
My doctor said that one multilens and one mono lens worked together, but one multilens and one uncorrected eye did not work that well together.
I can see the computer very well. I spend a great deal of time using the computer. I found that the lowest computer screen setting worked best for me. The one where the desktop icons are largest. When using programs, I use as is or adjust them within the program.
I find that I read better with a white background and black letters. Sufficient light is important. Polarized "driving" sunglasses (amber) have been very helpful to me as I am more sensitive to light than I was with cataracts.
OS: +0.50DS Add: +2.50) (before surgery I was OD: -400-275*032 OS: -525-200*159 Add +250) but I can't read without glasses any better in the left than the right, so I'm not sure improving the astigmatism would help that much. I could care less about not wearing glasses, that was never a goal. I was just fed up with constantly switching glasses since I couldn't read with bifocals, and thought if I was going to go through the terror of surgery anyway for cataracts I might as well do what I thought would eliminate this problem. Even if I went through having the ReStors replaced and miraculously nothing went wrong I'd still have the dry eyes, which one doctor said I don't have and the other two said I do, but it shouldn't have been caused by the astigmatism repair, even though I never had it before the surgery. My trust in
doctors, frankly, is zero! Susan12345
BTW, did you know that being female significantly lowers the risk of retinal detachment? And your risk is quite low to begin with--actually much lower than mine. And getting older lowers our risk.
Susan, I hope you're able to stop blaming yourself for the mistakes of others, and you can then re-focus your energy on making your situation better. I'm so glad to learn that you've been referred to a doctor outside your HMO who is reviewing your case and making recommendations. Best of luck to you, and keep us informed.
Are you saying that most of the 20% of people who still need glasses after ReStors wouldn't if their doctors had done their measurements correctly? That's a lot of bad doctors! Given my level of trust in the medical profession, I can believe it, and yet, knowing how greedy pharmaceutical companies are, you'd think they would be doing a LOT more thorough training before giving doctors access to the ReStors if that were the case. Granted, the Alcon Co. gets paid for the IOL whether it works or not, but bad publicity is eventually going to decrease demand.
Anyway, thanks for caring. I have a 2nd appointment with the new doctor Dec. 8, if I'm able to get my medical records by then. I haven't a clue whether he's trustworthy or not and feel like there's no reliable way way to find out about him or any doctor until it's too late. All I know is that he (like my ReStor doctor) has been approved by the Alcon Co. to install ReStors and he (like my Restor doctor) has been on my local "Best Doctors" list.
Susan12345
I got the info on retinal detachment rates when I was researching "clear lens exchange". The rate of detachment declines after age 70, and it is higher for males than females. Myopia isn't much of a risk factor unless it's worse than -8 diopters. I had vitrectomy surgery, which does adds a little to my risk. I got a cataract as a result of the vitrectomy and did a clear lens exchange in my other eye.
I can understand your reluctance to trust doctors. Last year I developed double vision related to monovision contact lens wear--a fairly rare occurrence. I had several worthless, frustrating consultations with optometrists and ophthalmologists who had no idea what was causing my problem or what to do about it. I started doing my own research by typing "double vision" in Google. Once I understood my problem, I had a better idea of what would help. I ended up referring myself for strabismus surgery. Now I try to research medical issues BEFORE I see the doctor. It gives me a basis for knowing which doctors to trust--and which ones to run away from.
Dr. ReStor told me that he might not be able to correct my astigmatism 100% and that's why I might have to wear reading glasses after surgery "for small print". That's why I thought the 20% were wearing reading glasses. At the time that seemed perfectly reasonable, I was already wearing reading glasses, for READING, as a nearsighted person since childhood I had no concept that it was possible to not be able to take your glasses off and see the buttons on the microwave and of course no clue of the fluttering I get as my eyes try to adapt from far to near. He certainly never mentioned before or after surgery any further surgery to correct the astigmatism more. I suppose because he knew that my HMO wouldn't cover it. They covered the 1st astigmatism surgery because it was done at the same time as the cataract surgery, all I had to pay was $2100 extra for the ReStor lenses. The money was definitely never the issue for me though. I would NEVER have had multifocal IOL's if I had thought there was any chance of needing more surgery. It was scary enough knowing that you had to have both eyes done if you had multifocals, but I told myself, the 2nd cataract will have to be done eventually, I might as well get them both done and not have to worry any more. HA!!!!!!
I don't know why he didn't tell me all this. He's certainly not hard up for business, it takes months to get an appointment. Though he was new to my HMO at the time, one of the other eye doctors I consulted before him told me how incredibly lucky my HMO was to get him, so maybe he wanted to make the HMO didn't regret the huge salary I'm sure they're paying him. I don't know. Doctors are a bizarre species.
Susan12345
Susan you are not kidding. I was scheduled for surgery on my second eye many months ago. No mention of destorded vision, or any problem was mentioned. Then after the study report was in, it changed to, " risky destored vision and eye surgery before cataract surgery, and months of healing". It is hard to know who to trust. This was definately financially related to me. Study over. No need to finish the reduced rate patients, in my opinion.
Jodie, Can you tell me about your vitrectomy? Is it really that risy? My floaters are not improving from the PVD and I don't want to live the rest of my life like this. But I read many times how risky a vitrectomy(sp) can be. Can it be done while awake? Does it increase risk of a retinal detachment? I am just going into my 4 month after the PVD, but very little improvement. If after a year things do not get better, I was thinking about seeing a doctor for this procedure. Can you give me your opinion? Thanks much!
Sorry about your PVD, hope it improves.
Susan12345
I can certainly understand why you want to get rid of those floaters. If I were in your situation, I'd schedule consultations with one or two of the best retinal surgeons in my area to get their opinions about a surgical solution. (Try asking other ophthalmologists who they'd send a family member to.) That should give you more information for basing a decision as to how to proceed.
I was told that with the Restor, the middle is for close, opposite of the Rezoom.
I'd be interested in knowing your doctor's opinion about why the ReStors didn't work for you.
Somebody posted a successful Restor explantation done by Dr. Kevin Waltz in Indianapolis so I decided to make an appointment with him and took the trip to Indiana to see him. Dr. Waltz was able to diagnose the problem within minutes and confirm my hunch that the lenses were displaced in both of my eyes after a thorough examination. I was actually able to see the decentralization of the Rezoom lenses in the photographic pictures he took of my eyes and could see the refractive misalignment in the digital printout after a test for refraction was done. The pictures told the whole story. I always suspected that there was something wrong with the placement of the lenses but no one was able to pick up on this. They all blamed the problems to adaptation, dry eye, astigmatism, etc.
Surgery to reposition the lenses is scheduled for late December for the right eye and 3 weeks later in January for the left eye. The procedure for repositioning is less traumatic and safer than removing the lenses and I have full confidence that Dr. Waltz will resolve my problem. Dr. Waltz is an Array lense implantee himself and I was amazed to see how well he could see in all light levels. I will keep you updated and let you know the outcome of my repositioning surgery.
The moral of the story, is keep looking for someone who's qualified and understands the technology..
Susan--What's this about blindness? From the info you posted, your chances of experiencing a retinal detachment are less than 1.5 percent if you explanted your "horrible" lenses. That's really not much different from your chances of retinal detachment if you don't explant your ReStors. But even in the extremely unlikely "worst case scenario," having a retinal detachment doesn't make you blind (unless you decide not to treat it). Retinal surgeons repair detachments every day. One of my coworkers has had two retinal detachment and currently enjoys good vision.
Susan, in your case, it doesn't really matter why your ReStors don't work for you. You've found a surgeon who can exchange them for lenses that will make your life easier and potentially more satisfying. Go for it!
Jodie, the doctor said that there was a 1 in 1000 chance of total blindness in that eye ANY time you went into an eye for surgery, even regular cataract repair. The additional risk of retinal detachment with an explant is just when doing the surgery, above the lifetime risk, because of the risk of capsule rupture. Plus there was a list of additional risks like corneal decompensation, which I didn't really understand, but I'm sure it's definitely not good. Plus, if I do decide to have it done, I've got to figure out whether this guy is really the best one to do it and I just don't know how to determine that.
Blue, what tests did Dr. Waltz do to determine that your IOL was positioned incorrectly that the previous doctors didn't do? I've been told by 3 doctors now after dilated eye exams that my IOL"s were centered perfectly, but it sounds like you were told that by several doctors as well. Good luck on your surgery.
Susan12345