Cataract :: Deciding To Have Toric Lens Removed
Jan 8, 2016
I have a complicated history. February 2013 my retina detached right eye. I had a vitrectomy and a lot of laser in left eye. The following January (2013) I had cataract removed and a toric lens implanted. Having always been a high myope with a lot of astigmatism it was a miracle. Only real problem was the disparity between my eyes and need to always have contact in left eye if awake. WIthin 5 weeks I had developed posterior capsular opacification. After the YAG I could see for a couple of days clearly again and then vision started declining again. I developed an epiretinal membrane and macular hole so I got to experience another vitrectomy in September of 2013. Since then my vision has declined. Multiple attempts at contacts have been frustrating. My dry eye makes soft contacts very unstable throughout the day and at times the vision with the soft is worse than without it. Multiple RGP's have been attempted. I wear and RGP in my left eye. Glasses have been tried but I must wear contact in left eye because the difference between eyes is too great. Unfortunately glasses don't work great because even that subtle difference of one eye corrected in front and one on eye makes my brain wacky. So my options are according to doctor "live with suboptimal vision or be willing to take a risk." PRK was mentioned but favorite option is to remove lens and have plane lens put in front of capsule then have vision corrected with RGP's. I am nervous about this with my history of scarring and retinal damage. Has anyone experienced this. I can be corrected to 20/20 in the eye.
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I am bored with my spectacles, and planning to get contact lens, i know its advantages but don't know its disadvantages.
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Can someone please help me what are the disadvantages of using contact lenses?
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I am 24 years old and have an (apparently) odd eye colour. My sclera has turned blue- only the visible portion- it appears almost like a blue contact lense. if i move my eye there is a clear defining line between white sclera and blue sclera.
After several people noticed I went to the Dr who had never seen it before. They ran blood tests for iron and liver. only issue was slightly lower ferritin at 17 (not enough to treat). The Dr has no clue, and neither do any other doctors in the practice. Optician says eye health is fine, and they don't know the cause either.
Has anyone else encountered this?
I also get joint pains, digestive problems, and fatigue.
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I started having vision issues just before Christmas. I went for a visit to my Ophthalmologist today. Turns out my blurry vision issues are a result of the cold air and my Dry Eye Syndrome. I did leave with a prescription though for mild correction for distance.
The doctor told me I could fill the prescription or not, it is up to me. How do you decide when your vision is bad enough to start wearing glasses? I don't mind the glasses themselves, just wondering if it is worth the cost yet. Thanks for your input.
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Who here has been on the NuvaRing?
After discussing my options with my doctor last week, I decided to give it a try. So far so good. I had some cramping in the first few days, but that's completely gone now and I haven't noticed any other side effects.
Part of why I chose NuvaRing is I don't have to think about it very much. Also, my doctor doesn't like the implant, and would rather save an IUD for last if I don't find something else I like. She did mention Depo, but I didn't want that because of what I've heard about bone density loss and weight gain, neither of which I want. Another reason is my doctor said she has lots of patients with success skipping their periods on the ring, and that's something that's important to me. If I could, I'd stop my period until I was ready to get pregnant.
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I don't know much about which brand of oral contraceptive I should use, partly due to nurses at planned parenthood not being very informative. Since there are many MANY different brands I figured I would just shout out my ultimate dream pill and see what suggestions you guys can give me. I want a pill that won't lower my libido and increases breast size. Some have taken me from a b to a d, some only half a cup. Would love that extra boob again lol thanks guys!**also I tend to get a little emotional so I'm not too sure where to go from here.
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After doing the best I can to ferret out the risks vs benefits of cardiac catheterization. 92% of my brain says, "No." That niggling 8% is a real pain.
I am female. I am over 60. I have not had a myocardial infarction, (that they're telling me about anyway). I have some stress wall hypertrophy, but that's pretty much it. If I could get the physicians/cardiologists, to give me better evidence of need for such an invasive procedure, I might consider it...however...
I know me. Just having the procedure would be psychologically, and, therefore, physically, ruinous. I think I understand - but who can understand this really - that choosing not to have the catheterization, and whatever may happen as a result, means I might sign out quite unexpected. But is this a better way to live? I think so.
I have not felt "well" for at 7 years. (I'll spare you the ailments). However, I don't get colds, flu (no vaccinations)...I don't have hypertension. I'm told I have angina, but I am convinced that the post-meal sensations I get are due to gastric/diaphragm...more on that order of things. I don't have frank chest "pain."
I'm figuring that it will be a complete crapshoot to refuse the catheterization, but I am 100% certain, that there is a better chance of me surviving an invasive procedure if I don't die before I have it, then lending myself to what looks like a never-ending routine of invasive procedures.
What I'm currently hoping for, but have been unable to get, is a cardiologist who will agree to fully monitor me; one who truly understands the various medications available and who would find one that is best suited for this particular body, and who considers cardiac catheterization, et al, a last resort, rather than a first. (Nice fantasy).
So far, I've had the general practitioner I see, attempt to scare the hell out of me without telling me on what evidence he was doing so. (I would change to another GP if there was another one around). That kind of tactic is not only useless, but demoralizing. When it comes to "heart," demoralization can, without a doubt, lead to "heart trouble."
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In 2009, I was diagnosed with Thoracic Osteoarthritis, Degenerative Disc Disease, and Fibromyalgia - and in November 2015 diagnosed with Cervical Radiculopathy. As you see, I have dealt with chronic pain for a long time, and I am tired of it – it’s exhausting and limits my day to day activities.
Anyway based on my MRI results and my physical symptoms - the surgeon diagnosed me with Cervical Radiculopathy and *suggested* a Posterior Cervical Decompression (PCDF) as well as an Anterior Cervical Discectomy with Fusion, ( ACDF). No pressure … he told me to just think it over and referred me to Physical Therapy.
Since the diagnosis, I am doing a ton of research and educating myself about my condition and the surgery.
Last week I asked my physical therapist what she thought of the surgery and she said, “I had time to have the surgery later”. (I’m 63 and not clear about what “later” even means This week my primary care doctor said outright, that I do not want this surgery because it may not relieve the numbness and pain, and does nothing for the arthritis in my neck, and there will be issues with scar tissue and that my condition is not that bad – yet. He suggested I get a second opinion. I agreed to get a second opinion.
Cervical Radiculopathy Timeline
January 2015 I developed a pinch nerve in the left side of my neck along with the slow progression of excruciating numbness and/or pain in my arm, fingers and thigh. In June 2015, my primary care doctor diagnosed me with pinch nerve and referred me to PT along with the suggestion that I get a back massage. I had tried PT before for my osteoarthritis and hated it. So, I decided to try yoga instead.
Through yoga, I relieved most of the thigh and neck pain and increased my range of motion. However, the numbness and pain in my fingers and in my arm became worse - along with the loss of grip strength. I informed my primary care Dr. in Oct of 2015, he referred me to an orthopedic surgeon, who of course ordered an MRI.
As I said, based on the test results, the surgeon suggested surgery but wanted me to first try physical therapy, this time I went. I started twice weekly therapy sessions in November 2015 and so far it’s effective. After 6 weeks of passive exercises, my arm pain had diminished significantly and the numbness decreased to a ‘low buzz’.
Because I was progressing so well - the week of Christmas 2015 the therapist changed to more aggressive exercises (10 mins on the treadmill, resistance bands, etc) I felt ok while there. However, by the time I returned home after the session the pain in my neck and back was out of control. I had learned many PT pain intervention techniques and I tried them all but the pain escalated. Numbness increased significantly in my thumb. In addition to that I now not only have pain on the left side of my neck but also the right - along with a considerable decrease in my range of motion on both sides of my neck. My grip strength decreased almost immediately and I am dropping things again. Thought it best to cancel my next appointment, ha-ha! Although I feel better, today I am still in pain - most movements makes it worse. At this point, I’m confused and not sure what to do next. My next PT appointment is on Jan 5th and I see the surgeon on Jan 19 to inform him of my decision.
My questions.
1. Without ongoing physical therapy –(i.e. the rest of my life) will the symptoms of Cervical Radiculopathy return? (Anyone have experience with this?)
2. With degenerative disc disease, overtime, will my disc continue to lose height and stack on top of one another causing even more pain? (So far because of this I’ve lost 2” in height.)
3. From the point of being diagnosed with Cervical Radiculopathy what is the longest time anyone has waited in deciding to have the surgery or not to have surgery?
4. Why would waiting for the symptoms to get worse be beneficial to obtaining a positive outcome or to justify the surgery?
5. Finally, why are some medical professionals against having this surgery? Has anyone experienced being discouraged from having the procedure and how did it influence your decision to have or not have the surgery?
I thoroughly understand this is a major surgery with a very rough and long recovery period. To be honest at age 63 – I am more worried about recovering from the anesthesia and if my body can withstand the actual length of the surgery, and those factors are certainly not going to get better as I age.
I also understand that I need to rely on the medical professionals’ opinions however, I have been ‘burnt’ in the past with so-called medical opinions. That is why I am seeking experiences related to this from ‘normal’ folks ---I need a different perspective from people who have dealt with this process.
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I had cataract surgery five days ago. On taking the dressing off the next day my vision was brilliant and no discomfort.
On the morning of the third day (Saturday) it felt as if I had something in the outside corner of my eye and that the clarity of vision was somewhat less. As it didn't wear off I called the out of hours ophthalmic nurse. She first asked me to check for an eyelash or anything in the eye. Her second suggestion was that I could have a sensitivity to the cheapo NHS eye drops with preservative in them.
We agreed to leave the situation until after applying the next eye drops. Things were no better when she called me back. She offered to get the on call eye doctor to see me at the hospital.
I did not feel that it was urgent enough for that and that I would leave it until today ( Monday)
The discomfort worsened over night and I called the daytime contact number. They took my details and will pass them on to the eye clinic and someone will call me back...but it might not be today.
The feeling is rather like when many years ago I wore contact lenses and I put one in wrongly.
Has any other reader had the same sensation?
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I'm have had a corneal transplant & cataracts in my left eye at different times. Now my eye specialists wants to do both the corneal transplant & the cataract at the same time. I want to have it done but my husband is against it. If my husband makes me not have it done will I lose my eyesight completely in my right eye.
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After 2 weeks from the surgery I developed Central Macular Edema, it manifested itself as a round gray spot on my field of vision and could not read also with the glasses because everything was blurred also because my right eye has still the cataract. The ophthalmologist prescribed me Acular to take together with M for another 2 months and asked me to go back for check up at the beginning of April. I was forgetting: last year I was found to have a slight macular degeneration, the dry type and she said not to worry. I would like to know from other people who had the same problem as mine. Is it likely that after 2 months I could be clear of it? Also anyone can tell me how long they have to wait before taking a flight abroad?
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I have Cataracts in both eyes and had surgery three weeks ago with Crystalens implanted in right eye.
Apart from one hour after surgery when my sight in the right eye appeared wonderful I have been unable to see properly. All detail is blurred; I can see my outline three feet from a mirror but no detailed features; straight lines are distorted; (i.e. door frames picture frames etc) and vision from this eye appears to be via a green glass window.
After the first week I had further laser treatment to remove cloudiness but my eye sight remained exactly the same with the same symptoms and distortions.
Yesterday I was diagnosed with Macular degeneration (wet) and given an Avastin injection in the eye and advised that it could take several months for me too see from this eye.
I am a male 66 years old and very worried, particularly as I also have untreated cataracts in my left eye. I have also lost confidence in the surgeon in view of the change in diagnosis and the failure of the original surgery.
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I had cataract surgery after a vitrectomy for retinal detachment. The eye required a scleral buckle after surgery and an oil bubble to support eye shape. The replacement IOL now has oil residue on it which makes vision very poor. Where can you find the best surgeon to do the surgery and is it advisable
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I am in day five after having my first I done and am experiencing dizziness and anxiety. Could this be from the vision in one eye being different. I feel like I can't focus on anything. I know I shouldn't compare myself to others, but my Sister drove and went back to work after 3 days. I would be afraid to try it now.
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On Jan 6 of this year my ophthalmologist advised me I had a macular pucker in my right eye. During that visit and prior to her diagnosis I received an eye chart test in which I noticed for the first time that straight lines were slightly wavy in the right eye.
My doctor’s diagnosis was that the same right eye had a cataract and I should see an eye surgeon to discuss possible surgery.
A month later I had the cataract surgery and was on a regimen of eye drops (pred Forte & Ilevro)
(one week prior and three weeks after the surgery).
On 3/21 (my last post op visit) I mentioned that the cataract surgery has improved the vision in the right eye but I have noticed the waviness of straight lines due to the macular pucker in the same eye seems a little more pronounced. I was given a test to see if the pucker had worsened and was told it had but only slightly (foveal thickness was 429 from 437 on Feb 6
I was also told to continue with the pred forte but increase to 3 times a day and the ilevro twice a day.
The doctor said it was possible the cataract surgery may have affected the pucker a little and that I should see a retinal specialist in several weeks to learn if the pucker size had changed further.
Am looking for a second opinion on this course of action and to see if anyone has had a similar experience with cataract surgery affecting a macular pucker
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Diagnosed with Macular Pucker. Retina specialist had me try steroid drops but did not help vision in fact made it worse. So surgery is now recommended. I would like to get a second opinion. Also have developed cataract in that eye and wonder if that can be done at the same time.
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Have the beginnings of cataracts but had 4 cut RK with recent longsight shift. Terrified of cataract surgery as there seem to be so many horror stories of it going wrong. Anyone had it go right after RK
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I had right eye cataract surgery 15 months ago, but protein building required capsulotomy. Unfortunately, the doctor cut a square out of the back of the capsule with a laser which floated in visiont (duh!). Further laser blasting left lots of floaters in eye.
Today had Vitrectomy to remove vitreous and gunk. However, I notice now that vision in that eye is tilted 30° and shifted down from where it should be.
No pain or flashing lights. WIll be calling hospital Friday morning (too late tonight)
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So, November 21st 2014, I got the nexplanon implant birth control so that I would be able to be with my partner without any worry of children. It seemed like the perfect decision at the time. Three years from now I will still not be ready most likely and I don't have to remember to take a pill every day or anything. What a dream, right! No. I was very wrong. The nexplanon may work for some people but for me, so far, it has been terrible. I know that it's new chemicals in my body but I've been vomiting non stop. I can't get out of bed anymore and I'm sleep deprived due to mind numbing headaches. I've also been bleeding everyday but that's not really what worries me the most. I can deal with the bleeding but with the vomiting and headaches? No! That's not what I signed up for. So my question is how soon can I get this removed? I have an appointment for a check up on December 4th but will I have to wait for my arm to heal up before they can numb it again and take it out?
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I'm just wondering when the ENT cleans out your ears, is it possible that the Dr can mess up the ear crystals that can cause vertigo?
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My surgery went well. Surgery was at 11 and I was discharged at 1:30. They did an endoscopy of my upper GI and all was clear. I am pretty sore in my abdomen area and omg my shoulders are killing me from the gas, and of course I have a sore throat. All in all I'm good...had some soup last night, did fine and I have been juiced today. Already the pain that went through to my back for months is GONE!! I had stones and sludge. I'm so in hopes my reflux will improve, its so bad I get acid in my ears and my mouth stays swollen with a scalloped tong. The worse my Gallbladder got the worse my reflux got.
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