Left eye symptoms and conditions

Fatigue, flashing in the left eye, worsening migraines:
I have been on Arimidex since July, 2007 (after lumpectomy in January 2007, chemo, a mastectomy in same breast in August, 2007 followed by radiation) and seemed to be tolerating it quite well, except for the fact that I wanted to go to bed at no later than 9PM every night.
Recently, however, I had noticed retinal problems in my left eye (could also be a result of my nearsightedness and my age --61) and worsening migraine attacks which I could not relieve completely with my usual medications. I did research on Google and found that Arimidex could indeed lead to worsening of headaches and perhaps lead to retinopathy as well.
This morning I decided not to take the pill and called my oncologist's office to find out what he thinks about stopping it for a while.
I have also made an appointment with a neurologist since I haven't had a brain MRI since 1987 (to rule out other causes than migraine for my headaches).

Ive been on Topamax for almost 3 years. Was on 100 mg/day for 1 1/2 yrs. Couldn't take the spaciness so I went off of it. A new Dr. put me back on 50mg/day 6 months later because my headaches were so bad. I'm doing great. Headaches are less frequent. Maybe 2-3 per month but not so violent. But lately I've developed this twitching under my left eye. It's constant. Could it be the Topamax???

UPDATE from Yesterday)))>>> well thanks to everyone i quit taking it yesterday BUT!!!---> today when i woke up i had a horrible head ache and it seemed to be coming from my left eye. i looked in the mirror and i have a really weird yellowish glazed tint in both my eyes and in my left eye a blood vessel has burst. i also noticed ive developed a skin rash on my right side of my stomach and on my left calf. My joints kept me up all night in constant pain which felt like someone was ripping apart my ligaments. I had a minor anxiety attack last night (Ive NEVER had anxiety before) and my body just feels weak, drained, and i keep getting really weird muscel spasms in my upper thigh. I tried to go out to the store earlier and as soon as i stepped into the sunlight a migraine hit me, and ive never been sensitive to light....Ive had a feeling of helplessness and worthlessness more in the past 24 hours than i have in a year. Im also experiencing horrible lower back pain and stomach pain around where my kidneys are.... I did have a small amount breast tenderness when i woke up and im not sure if that's another side effect...(no im not pregnant, had multiple urine tests in the last week)...I think ive only went potty maybe once today...and that was at like 9am...its now almost 9pm. Im pretty sure if this isn't over with or doesn't improve by 10pm im going to the hospital.....i cant drink water and im pretty sure im getting dehydrated....my skins turning pale, i have dark rings around my eyes.....etc.......has anyone else suffered with these things? Levaquin is by far the MOST painful, riskful, antibiotic ive been on...They should definitely take this sh*t off the market!!! =[[

After a year of battling effects from an eye injury, an optho-neurologist finally came to the conclusion that I had orbital inflammatory psuedo tumor. I was told to take 60 mg immediately and then take 2-40mg doses (AM and early afternoon). On Friday, July 18th I took 60 mg at 6:30 p.m. and was so nauseous and barely slept. That next day I took 40mg in the morning and another 40mg around 2:30 p.m.. Although I had been, throughout the year, experiencing pain in my left eye and cheek..what I experienced by 4:00p.m. that next day was more severe than ever. I started having shooting pain and a headache so excruciating that I was in tears. (I had two children naturally).
By 10:30 I had several hours of this pain when the worst happened. The left side of my face drooped and I had difficulty speaking. By the time I got to the hospital I could not move my left arm and left leg. After five days in the hospital and every test imaginable (cat scan, MRI, EKG, etc) they ruled out all stroke, MS and anything else that would show up on these tests. During the hospital stay (although they did not cite prednisone for this event), they started tapering me off. I went from 80 to 50 in one of these days and thought I would DIE. There was no pain reliever/narcotic strong enough to take away the headache. I spent ten days tapering and prayed every day for the end. Sweating, no sleep, crying and did I mention...my headache has still NOT gone away. I have a couple of hours here and there without this pain but for the most part I have been in this hell even after my taper. The clincher is that NO ONE at the hospital or afterwards would admit that this was a side effect but they also could not provide a response. It took three weeks for me to work my way back to walking and using the left side of my body. Has anyone heard of this before? Good luck to all of you, it has meant a lot to read your comments.

Shortly after I began taking Wellbutrin XR my left eye bagen to twitch. I discontinued the medication and the flinching stopped. Three years later my eye is twitching again. I am not sure if there is a correlation or not. I had an eye exam and have no problems with my vision.

I gotta tell ya this is scary. I am a 30 yr old guy my wife is 27 we have four children.Our last one was born Mar. 2007 She has been on Yasmin 6months or so.She has never been regular on periods. Well a few weeks ago she started having massive headaches.As of June 31st her doctor said she has migraines. Well by July first her left eye went blurry by the 2nd she has lost vision in both eyes.She only sees light and is very cloudy and can see shadows. We made 3 trips to ER. They did Cat scan and it was neg. the doctor said she might have even had a mild stroke because her left cheek went numb. By the 2nd we were in ER again because of total vision loss. They did a lumbar punture and no Meningitus. cat scan again neg. blood work neg. except UTI sound familiar ladies??? By the 3rd we visited her doctor and she passed out and was rushed by EMT to Hosp. They did and MRI,MRA,had a eye Doctor called an ophthalmologist clear her of vision problems.She has talked to a neurologist. So here is a 27 yr old female with all the test's coming back normal but she can't see.They even had a psychiatrist talk to her because she is on Prozac because she has PCOS and had half her ovaries removed and almost died.They even suggested that she had conversion disorder(google it).Finally I decided to check side effects for all her meds. When I checked this one I almost jumped outta the chair.She has about 10 symptoms. But before I get too excited has anyone had vision loss for a period of time and did it come back once off of it?? I'm throwing these away

i have been on the nuvaring about 2yrs give or take. Just about 2mths ago i discovered having head aches. They have not gone away ever since. I have have blood work done, and mri. the mri showed i my jaw pops out of place when i open my mouth to wide. The doctor says that it looked lik TMJ but there to independent things. So he suggested to stop using my birth control. I called my gyno, she said that people have had cases of getting migraines but its unusual to be on it for so long and suddenly develop migraines. I have been on lots of medication nothing seems to work. She told me to stop taking it after my next menstrual cycle, im praying that this will cure my migraines.

I had the Mirena put in six weeks after having our daughter, on June 30th, 2006. I never was able to loose weight, and felt very bloated, moody, with pains in my sides (ovary level), and then in the Fall of 2007, I noticed a significant loss of vision in my left eye. I went through $40,000 worth of hospital visits, and one 8-day stay, to figure out that the Mirena had caused a rather large blood clot to form on the outside of my brain in the main vein that crosses over the top outside brain. I have suffered from multiple ER visits with migraines lasting up to 72 hours, even after shots and meds. I have been going to the University of Colorado Hospital for treatment and it has taken over six months to get me on a medication regiment that will hopefully alleviate my debilitating headaches and now am living with the possibility that my vision may never get better in my left eye. The Dr.'s I have seen: an eye surgeon, a Neurologist, a Neuro-ophthalmologist, a Retinal Specialist, and the multiple local MD's. The tests run on my body and head have been very extensive, including blood tests, multiple MRI's and the final MRVenagram that tests the flow and drainage of and around my brain that found the blood clot and have ruled out everything from MS, to Pseudotumor Cerebri (which is a lifelong disease offering only pain management for the most part), as well as a macular deterioration related with people over fifty, not 24, they have also ruled out any pre-existing tendency for being prone to blood clots . This has been the scariest thing of my life and so consuming and debilitating, that I would never recommend the Mirena to anyone. I have missed so much work and the traveling to doctors have been a drain on our financial situation. This kind of information needs to get out there because Dr's are denying any relation to the Mirena. My Dr's have definitely diagnosed my problem as the Mirena. The swelling of spinal fluid was my body trying to protect itself and that swelling caused such great pressure on my optic nerve that my macula, where a person has central and fine detail and focusing, wrinkled in a layer of my eye that cannot be operated on. I can no longer read out of my left eye and the stress that created for my right eye is a contributor to the migraines. I also see double at night, when lights or signs are illuminated by the headlights of my car. I am seeing two images! This is very hard to accept and not being able to read for very long also upsets me. The likelihood of my vision repairing on its own is slim to none. Thanks Mirena. SO please, please help the word get out!!!! Also caution anyone you know who is planning on getting the Mirena, or who has one in to be aware of any changes. My experience has been very extreme but maybe women out there are going through the same things I have been and no one will recognize the relation to the Mirena. I am only glad my Dr. was willing to admit the Mirena was the cause.

My 70 yr. old mother started taking wellbutrin on March 26 2008. just to quit smoking. 150 mg. in the morning and 150mg. in the late afternoon. she did not quit smoking. I was noticing she was starting to kind of stagger when she walked almost as though she were drunk. and she would shuffle her feet and almost trip over them. keep in mind my mom is a very active, walks everyday very fast and looks 50! On April 17th she woke up in the morning and told me she felt very tired and just wanted to sleep. this worried me because this is not her norm. so I let her sleep. well she kept on sleeping. I went to work..came home and she was still sleeping!! I woke her up and she said she felt very panicky and was shaking very bad. I looked into her eyes and they looked jittery. She even said her left eye was very blurry. something was not right. I took her to the ER. They kept her for 3 days. did every test imaginable. every test came back perfect. no stroke,, NOTHING wrong!! she was sleeping the entire time in the hospital. They released her and said the only thing they could find was a slightly elevated thyroid. we have an appt. for that may 4th. so..as her heart is pounding and she is still very weak and can barely walk..they release her. she comes home and forces herself to walk to regain her strength. still on the wellbutrin. hospital still gave her it because we had no idea that wellbutrin was the problem. she had taken it many years ago and it was fine. she sometimes forgets to take it and she remembered yesterday that she had not taken her wellbutrin for a couple of days. so she took one. a couple of hours after that she began to shake again..her eyes looked weird again. she was very unsteady in her walking. very scared. well. today she is sleeping again. I am on here reading ALL THESE SIDE EFFECTS!!! I told my mom to gradually stop taking this pill!!! I really think this is what is causing all her problems. NO MORE WELLBUTRIN!! I will let you know how she is doing as she gets off this pill.

Could this be Mirena effects. I have been to er twice in a week due to severe dizziness, eye sight loss in left eye and numbness in left arm - they did cat scan chest xray Mri blood tests and nothing seems to be wrong. I am so dizzy I cant even go to work or the store. Called 911 myself one day cause i really thought I was having a heart attack or stroke - still no answer - glad to have found this site - not feeling so crazy now!!!

Could this be Mirena effects. I have been to er twice in a week due to severe dizziness, eye sight loss in left eye and numbness in left arm - they did cat scan chest xray Mri blood tests and nothing seems to be wrong. I am so dizzy I cant even go to work or the store. Called 911 myself one day cause i really thought I was having a heart attack or stroke - still no answer - glad to have found this site - not feeling so crazy now!!!

Uh, been on it three days and woke up unable to see in my left eye.

Neuro said it's the Soma. Not only did it blur my vision but gave me headaches, made me feel dopey and didn't take the pain away from my shoulder.

I began to experience upper body itching (arms, back, and upper chest after taking TobraDex drops for two days. (perscription was for left eye, 3x per day for 4 days) After 8 days the itching still does has not gone away.
The level of itching is similar to what you would experience with a low level sunburn with light skin flaking. It's rather interesting, I don't really feel an intense itch on my back, but when I start to scratch it really feels good to just scratch and scratch. And no, I do not have sunburn.

My throat started to tighten like someone with a fish or nut allergy.
My left eye leaks a sticky liquid and the lid is starting to droop. The lid also stick to the eye or feels like it, the eye feels like its fluttering. I have server Edma, I can hardly walk and cannot get rid of it even with water pills.

I just discovered this after 3 months of total misery, 7 different doctors, multiple tests, 1 hospitalization, 16 pound weight loss, almost lost my job, etc., etc., etc.. I want to know if this will have permanent effects on my body and heart and will I ever be the same again. I have been back on the brand TOPROL XL for 9 days now. Keep in mind I didn't know what was happening to me, I never thought twice about the switch to generic, it was cheaper and I also had a lot of stress going on in my life at the time.

My pharmacy switched my "Toprol XL 50 mg" to a Generic one called "Metoprolol Succinate ER 50 mg" (manufactured by Sandoz) in December 2007. I have been on some form of Beta Blockers for years due to PVC's, AVNRT, Bigeminy, Trigeminy and Couplets. NOT High Blood Pressure. In my case I get very symptomatic from the arrhythmias: very low blood pressure, chest pain, fatigue, blacking out. I've had EP studies and attempted ablations in the past, but they were unsuccessful. For the last 2 years I had been under control on this med. Within a week of starting the new generic, I was at my eye doctor because my left eye went from 20/20 to 20/60 and was so blurry that I felt like I had suntan lotion or something in it. The new symptoms just kept coming. Since Dec 07, I have been to a Neurologist, Neuro-Ophthalmologist, Endocrinologist, Gastrointerologist, Ear Nose and Throat Doctor, Cardiologist, and many more. The generic form caused my arrhythmias to come back with a vengeance, I got depression, I couldn't sleep, my chest hurt, my BP was like 85/45, I lost 16 pounds and couldn't eat. I was almost passing out, seeing stars, I had bigeminy/trigeminy day and night for days on end, I was crying for nothing, very moody, I was coughing and wheezing, I had tingling in my arms and hands, loud ringing in my ears, I couldn't concentrate let alone think. I had tons of blood work that the doctors said, "just didn't look right". Upper GI test discovered a hiatal hernia, MRI discovered brain lesions, I had a high red blood cell count (but not anemic), my ferritin was high, my blood sugar was high, I was tested for MS, Lupus, thyroid, everything under the sun and was borderline for these diseases! I thought I was going to die, I had never been depressed in my life and this was the worst. I was beginning to think I was a hypochondriac. But, it was all there on paper, all the tests showed something wrong, but they didn't know what.

I googled Toprol brand versus generic and found out that it wasn't just me, thousands of people have had these same reactions since they started making Generic Toprol. Please read up on it, everyone who writes their story can't be wrong (there is at least one from every state complaining of the same thing). I've been taking the old TOPROL XL BRAND for the last 9 days and my arrhythmias have completely stopped, I have an appetite again and the depression has lifted. I hope it didn't cause any permanent damage.

I know this is probably happening to people everywhere who don't have access to the internet or maybe don't get out much. If you ask the pharmacist, they will tell you that they are exactly the same and they are NOT. The generic may work perfectly for you, but it doesn't work for all. In trying to figure out why I was so symptomatic, the doctors in the hospital took me off the beta blocker completely....I could have had a stroke or heart attack. I started back up on the brand name when after I googled it and realized that you can't just "go off" Toprol. I just wish I would have discovered it about 3 months ago. They thought for sure I had either MS or Lupus and were trying to rule out all the mimics of these very serious diseases. I'm going back to my doctors and have them repeat all the blood tests, etc. to make sure everything is back to normal.

I'm trying to get the word out.

I started taking 750mg of Levaquin last Thursday, March 20, 2008, for a strep throat infection that was not responding to 500 mg. of Penicillin. I took Levaquin last summer due to another bad throat infection and had absolutely no side effects. However, this time I am experiencing a raft of them, from awful insomnia and sluggishness and tiredness, to sever headaches and coughing. I suffer from depression and this is effecting my reaction to the depression medication. I am feeling more depressed.

A few days ago, my head started to hurt near my left eye, and my skull became very sensitive on the top left side, midway between the middle of the skull and my left ear. If I cough, it feels as if my head is about to explode. To make matters worse, whenever I try to speak, I start coughing , which in turn hurts my head. My head is painful to the touch.

This is awful. Can anyone help me out with some pain relief or something?

Mikal

I was put on Advair 100/50 about 5 years ago and took it faithfully twice a day. I started having hoarseness and several times felt like I was having a heart attack.
I also noticed a trembling in my right hand which I did not know what to attribute it to. I could not hold anything in my hand before gradually dropping it.
I also started having leg pain which would grow worse at night and I couldn't sleep through the night. I had to get up a nd take some ibuprofen to get some sleep. I blamed it on my spinal stenosis.
For the past two years I have had an eye problem. I am losing sight in my left eye. The doctor sent me to a retinal doctor last year and I went thru all kinds of tests. He thought it was a wrinkle in my retina. I was examined again this year and it is the same.
This year my doctor couldn't figure out what was causing this and had a brain MRI done. This showed nothing.
I have slowly stopped taking the Advair and my leg pain has gone away and I am getting some well needed rest at night. As to my eye problem, there still is a Question. I will not go back on Advair again.

AC
Estero, FL

I am 42, no children, never pregnant.
I had Mirena inserted about 7 months ago.

I thought I finally found THE REMEDY against heavy periods and condom use.

Since then I've had practically constant spotting. My period (heavy, as usual) followed by spotting. The first couple of months continuous blood loss, the last 2 months it was 3 weeks of bleeding (1st week heavy), only 1 week not.

Because of all the blood loss, there is no doubt I have am low on ferritin, thus and suffering from an iron deficiency. I am tired and lack energy. There is no drive to take any action whatsoever. Could be lack of iron, could be Mirena...

I wear contact lenses and had a left EYE that showed bubbles, the surface wasn't flat anymore. My eye was irritating. Not suspecting/thinking of any relation to Mirena, I went to see 3 different ophthalmologists, 5 visits in total. I took every kind of medicine you can imagine against viral and bacterial infections (as heavy as Prednisolone) etc. They only made things worse. None of the ophthalmologists actually found the origin of my "bubbles". Finally, triggered by the fact that my eye problems started at about the same time as I had my Mirena inserted, I started to do some research on the internet and found a website describing scientific research on mice that stated that sex hormones influence the surface of the eye... All of a sudden all became crystal clear to me....

My THROAT is sore. Like having acid reflux. I went to see my doctor, had and echo done, went to see an ENT-specialist to looked into my throat with a camera. No one found anything special (except a red throat). I am practically sure that this phenomenon has to do with Mirena as well as I also have this problem since I have Mirena (and not ever before...).

I have all kinds of strange pains in my MUSCLES and JOINTS, especially in the lower BACK (which is hurting a lot like a hernia - I never have had back pains in that area before) but also my elbow and fingers and thumb. Sometimes my right leg is just paralyzed for a 10 secs and I am hardly able to raise my foot to walk. I feel like an old woman.

I feel SWOLLEN in my stomach, sometimes have slight pains or a weird feeling. I have the impression I can feel the IUD, especially at some movements.

I've had very sore BREASTS for some time (weeks in a row), but that's over now.

I sometimes suffer on and off from CONSTIPATION, which is very unusual (especially with my healthy diet (practically vegetarian, regularly organic food, lots of whole-wheat items, fruits and vegetables).

I always had some ACNE but it has gotten significantly worse.

I SWEAT at night and more easily during the day, something I never used to.

I lack sex drive and for the first time in my life I experienced intimate dryness. This is the best birth control I've ever experienced, because I have no LIBIDO at all...

Overall I am not feeling good / active / in good physical shape with my normal energy/drive. Also my MOOD has not been so optimistic as usual.

I am definitively going to have this Mirena taken out. Toooo many problems with this type of "birth control". It coasted me a lot of money and time, months of health problems. Back to condoms again. Something I am not looking forward to... but I do look forward in getting my libido back...

The thing that really makes me angry is that it is still is up to the women to stuff themselves with hormones. Why, in the last 40 years or so that the birth control pill exists (and I've taken it for 15 years or so, bloating me and killing my libido...), medicine never has come up with birth control for men???
I've had it with hormones. No more for me. I eagerly pass my turn is to the other 50% of the population. Let the male gender be suffering from lack of libido for some time (so women can make fun of them faking a headache...) and the rest of the side-effects of hormones. Women have enough problems with their period already... There's no justice in the way nature has arranged things and (male) scientists have only made thing worse.

I was taking Levaquin for a sinus infection. After taking the first dose of 750 mg, I noticed that I started having tingling and numbness in my hands and arms. After the second dose, I started feeling the same tingling and numbness in my arms, hands, and legs. Because I had been having severe headaches anyway, I started wondering if I had some kind of neurological problem and my headaches were linked to the strange sensations. However, I noticed that I didn't have any problems with my arms and legs until after I started taking Levaquin. Some of my other symptoms were: tightness in my neck muscles and sore muscles. I also remember seeing a flashing light from the corner of my left eye and floaters. I stopped taking Levaquin after just 2 doses because it began scaring me and I feared what might happen after my third dose. I can't afford to take any chances with my health. That's why I appreciate this post, and I see that I wasn't just imagining these side effects. Since I've stopped taking this medication I still have problems with my arms. They feel heavy like I've been lifting weights and the ache. A couple of times, I've had to take pain medicine for the pain in my arms because they've hurt so bad, it feels kind of like when you hit your funny bone and you try to figure out why they call it a "funny bone" because it's definitely not funny! My arms hurt so bad I couldn't lift them, and I could type or write so I just took some medicine (tremadol) and laid down. It's been weeks since I've taken levaquin, but I still I have sensations and aching and heaviness in my arms. Has anybody been off of Levaquin for a considerable amount of time and found that the symptoms go away? Please give me some hope! :) Thanks.

I live in Israel, and here in this country not only do the police do their duty incorrectly, but so do psychiatric officials.
I was in a bad state emotional, and that did not result in any obscene or out-of-the-order matter, but me having chosen to move on with my life was a bad idea since moving on meant letting go and kicking out of my life a she-devil that posed as a girlfriend.
she had connections and accused me wrongfully of stuff i didn't do, and since she had friends in the police force, I ended up being admitted to a psychiatric hospital, there I was forced to take 10 mg of ZYPREXA, every day, for a little more than a month and a half, after a couple of weeks i developed a rash on my head, and vibrations with palpitations.
when i stopped taking ZYPREXA, the rash continued, the vibrations when i go to sleep with the palpitations continue but are even worse,
I cant sleep, and when i do fall asleep I wake up every hour, if lucky i sometimes manage to sleep for 2 hours and then only wake up, and i keep waking up until i give up on sleeping, i get headaches, nausea, dizziness, i eat, and after 30 minutes to 1 hour i go the the toilet and diarrhea..
my left eye sees blurry, i hear much less in my left ear, and not to mention that i have no tinnitus, - all day long i hear an electric pulse in my ears, i am disconnected from emotions, cant concentrate, my memory is impaired, i cant seem to make myself do anything, i cant even figure out what i am feeling, my teethes health has gone bad, get mood swings which are not extreme at all, resulting in me not knowing what it is I'm going through, i think this Zyprexa ordeal as resulted in multiple sclerosis which hasn't been diagnosed yet, and i don't know what more else there is, since i am quite handicapped mentally emotional and physically i can do stuff, but for some reason i don't do anything.
bad dreams (when i do manage to get several minutes of sleep), and i feel stoned all the time. and this is not all, but seriously, here in Israel or overseas, who really gives a damn? and who can help these things go away??..Ive been told to wait (I've been waiting a little more that 3 months) for all this to go away, and nothing as gone away, instead more things slowly gather.
too bad there is no death sentence here in Israel, if there was I might try to get it, to end this suffering, though, what can i say, even dying is not something I can manage to get myself to do, I cant seem to actually decide to do anything, I just think of it, and in the meanwhile, my whole life is passing in front of my eyes, making me realize, this might be the ending of my life as I know it, and all i have to do about it is just sit and wait, either for things to change (cause i cant change them), or to die.

My father has been taking Warfarin for 13 years now 2.5mg a day. He's been complaining of headaches, heavy feeling in his head, dizzy spells, extreme fatigue,swelling of his legs, spontaneous numbness of his fingers, blurred vision, cold hands and feet, loss of balance and memory loss. I have spoken to his Doctors and no one believes him that the Warfarin is doing this to him. By the way, he was diagnosed with AF 13 years ago.

Does any one experience the same symptoms? what can he do? he is 77 years old.

Hello everyone,

My name is Tina and I am a mother of 5 children and I was diagnosed with a very rare disorder called "VKH" It is a rare eye disorder that only strikes like 1 in 1,000,000,000 people. I was put on Prednisone to help with this condition and to reduce the swelling in my eyes. I was put on 70mg initially and was tapered down to 40mg. then things did not go as well as to be expected and I was bumped back up to 60mg. I am so happy to read these stories but also saddened at the same time. I have been on Prednisone for 5 months and have gained 20 pounds and have the moon face, the acne, the hair growth and the horrible mood swings. My husband and I had our 10 year anniversary last week and I spent it all alone because of my moods.......
It has destroyed my relationships and my self esteem. I don't like leaving the house barely because I hate how I look and I am so depressed I am not the same person as before. I cry all the time because sometimes I wonder if taking this drug is worth it!!! What makes things worse is I wonder if things will ever go back to normal for me or my family again.................

O.k. Birth control has different effects on everyone, but I know for a fact this pill has been terrible for me. I used to be on Ortho tri cyclen for 10 years, but I needed to switch since I started spotting. Loestrin 24 fe helped with that, but I gained about 13 lbs in the first month & had a horrible depression which made me hate the world. I fought with everyone and I know its from this pill because I was off all bc's for 2 months & was so happy & normal. I know it put weight on me because I work out all the time & I have weighed the same for 10 years. I started on this pill & "bang" I'm huge. I was also hungry all of the time and my left eye twitches.I have one more pill & then I am switching to a new bc. Good luck if you're on this!

I've been on NuvaRing for a little over one year, and I have worn contacts for probably eight or nine months. In the last maybe, three months, I have noticed near-constant irritation in my left eye when wearing contacts. I read on the official NuvaRing site that contact lens intolerance is a side effect, albeit a rarer one to experience. I can't say whether this is actually from the ring or if I am just having problems. It happens with every new pair that I use, also, so getting out new contacts didn't solve the problem. Has anyone else experienced this contact lens intolerance? If so what was it like? Also, other than some random vomiting in the first week after reinsertion, I have had no other side effects.

On December 10 of 07, my 4 y.o. son had a tonsillectomy and a intramuscular injection of Kenalog - 40 in to his turbinate of his nose. a week later my wife and I noticed a problem with his left eye. Went to opthamologist and he said he was blind in his left eye. It is not recommended to give Kenalog by route of interburinate due to severe cases of blindness.