Eye Care :: Distortion Of Peripheral Vision
May 19, 2016
I'm wondering if anyone has ever experienced distortion in their peripheral vision. It's a bit difficult to explain, but it's almost like objects are a different shape in my peripheral vision than when I look straight at them. It often looks like straight lines are bent in my peripheral vision, or objects just seem to shift position but then shift back when I look back at them. Sounds very odd I know. I do have astigmatism on both eyes, but is this a normal symptom of that?
I have some other odd visual symptoms, such as trembling vision (straight lines appear to tremble) and light sensitivity. I had a virus about 6 weeks ago which I'm still struggling to recover from - achiness, fatigue, some muscle weakness. I've had blood tests, MRI brain scan and my eyes fully inspected by 2 ophthalmologists.
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I'm not particularly worried about this but I'd rather know what it is. I quite commonly will get, after stretching or getting up suddenly, flying black dots in my peripheral vision. These tiny black dots just appear, fly in a direction, then disappear. A bit like a swarm of flies in the corner of my eye except they keep appearing and disappearing individually. It might last up to five seconds or so. Then it's gone and I feel fine. I'm pretty sure I've had this for years.
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Ok so i have this weird problem with my eyes. Randomly (happened a lot when a year ago but stopped until now) i start seeing distorted lines. Kind of like millions of tiny prisms are rotating in a line. The lines often start in the center of my vision (making it hard to read) then migrate to cover the left or right side of my vision (but no longer the center)
It appears to be transparent but it is actually not due to the flashing of colours all over it.
They often take shapes but they seem abstract and are hard to focus on. Kind of like a multicolored distortion prism floater (the lines that you can see floating sometimes) although it grows to cover ~30% of my vision.
The "distortion" often stays visible (or moves out of sight) between 20 minutes and 3 hours.
I have not discovered any trigger for this "distortion"
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Anyone else experience flashes of light at the peripheral edge of their vision?
Over the last week I keep having them and swing my head round, like a flash has gone off.
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About a year ago or so I started to notice a change in my Peripheral vision. I found myself having to completely look to my right while driving because of a blind spot and I also noticed when I shaved my underarms I could no longer see them (very blurry) if that makes any sense. I didn't have and insurance so I had to wait. Fast forward to last month. I saw an Ophthalmologist thinking it was vision problems of some sort. Well, I miserably failed the test that checks for peripheral vision. He then looked at the optic nerve and didn't see anything that would suggest normal vision loss. He said I have lost almost all Peripheral vision in my right eye and a good amount on my left. He referred me to a neurologist that I will see this Monday. I was glad because I had also been having some issues with what seems like pinched nerves in the neck and shoulders, I thought it could be related to some nerve issues. So my other issue which I didn't correlate as being possibly related until today is that I have been having some major digestive problems that have flared up on and off since February. I am having a lot of indigestion, gas and constipation.. The constipation is pretty bad, sometimes I can't go and I resort to taking laxatives for relief. And I have this really annoying muscle twitching in my lower abdomen! It feels like a vibration, I have been having that for a couple of weeks now. I have been so miserable that I made an appt for next week to see a gastro doctor. But then tonight I Googled the vibrating issue and was noticing that there were many people on MS boards with similar problems. And then it hit me that there seems to be a lot of coincidences between my issues and MS. Now I am worried. Did any of you experience similarities before a diagnosis? And how are people diagnosed?
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Suddenly today I noticed that I seemed to have a film over my right eye and I was experiencing floaters. I had multifocal lens replacement surgery a couple years ago. Everything went well. It was the best thing I had done. I wore glasses since I about 7. I had a couple small floaters before the surgery but only saw them now and then. I had put some oil on my face earlier today and was wondering if some had gotten into my eye , would it have caused this to happen? I put saline drops in my eye and visine thinking this may have been the cause. trying to rinse out my eye. It did not help and am getting worried that something may be wrong. What worries me is that it came on sort of fast and has been the same all day. I also have been under a lot of stress lately, working long hours. Would really like some advice on what to do.
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I'm a 42 year old female and up to about August this year 2014 I only had single vision lens to read, watch TV, and work at a computer with. In August my eyes became very dry and felt like they were being tugged or pulled. I saw my regular eye doctor which told me I had dry eyes and put me on prescription eye drops. Soon I could tell I was getting some vision loss ex specially in my left eye. I also began to notice a "pinwheel" or something like a reflection of a ceiling fan in a droplet of water in both eyes in the outer upper corners of my eyes. I've seen my regular eye doctor about four times, a retina specialist twice and another eye specialist once. I also had a MRI but nothing has been found. I also had bifocal glass made by my regular eye doctor. Wear them for three week and I felt things were worse so I went back to my old single vision glasses. Has anyone had or heard anything like this? I am a mother of a special needs little girl that takes a lot of care and I'm scared I'm going to loose my eye sight.
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I just had a mammogram and it came back with architectural distortion in the right breast. My doctor says not to worry, but go for a repeat mammogram. The nurses in the office said the report did not sound concerning too, and one receptionist had this and it was the result of the mammogram having the distortion not the breast! I am so scared as reading on the internet does say that architectural distortion can be a sign of breast cancer. Has anyone had this show up on a mammogram? Can anyone offer some encouragement or experience with this?
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My mother had her thyroid and a benign tumour removed about 6 months ago. She lives 3 hours away from me, so I have seen her a few times but only for short intervals and we regularly speak on the phone. Since her operation I have noticed she is always tired (also due to her heart medication) and that she has become more of a glass half empty type of person. Recently my father had a heart attack (serious but my Dad is a trooper and is now recovering after surgery). I have spent the last week with my mother, and with her thyroid and stress of my father I became her personal punching bag. Her erratic mood swings, outbursts and obsessing over trivial matters are well documented relating to the thyroid in all the googling I have done. What I can't find is any information on her memory loss/memory distortion of the facts. To give 2 examples (of many): 1. My parents had a lawyer at the hospital to update their will, so I went out and sat in the foyer. I was on my phone looking at Facebook to fill in time and one of Mum's friends sat beside me. I put my phone away and chatted to her friend. On the way home Mum had a go a me because her friend told her that I spent the whole time looking at my phone whilst she was trying to talk to me. 2. After leaving my niece's 21st, my Mum tells me that one of my brothers was very cold to her all night and didn't talk to her. A couple of hours later as everyone is heading off to bed, my mother says "So (my brother) didn't talk to you either" with which I replied "Yes we did, I spent quite a lot of time talking to him". My mother than lost it completely and started yelling that I had told her that my brother didn't speak to me. Though I can't find any information about this type of memory loss, I am hoping someone might be able to give me a heads up. Also if someone has been told by a family member about their erratic emotions I would love to hear your advice on how to bring it up with my mother.
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My mother suffers from spinal distortion. Her muscles are sprained. Doctors say that this condition of hers is untreatable. I was thinking of trying with alternative methods like reflexology is. What do you think? Can it really help with her condition or not?
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Has anyone experienced a loud roaring low frequency noise in ear with hearing distortion. I woke up one morning in December of 2015 and felt like there was a gong in my head all sound was vibrating. I felt like I was in the front seat of a car driving down the highway with the back windows open halfway. I went to doctor and found I had lost some low frequency hearing in right ear. I was Put on steroids for two weeks. Got hearing back but left with this loud tuning fork/motor engine sound in my right ear and random hearing distortion in both ears. I am very sensitive to low-frequency sounds and any kind of motors, airplanes and low voices just don't sound clear. The motor engine stops when I speak and returns after my last word. When someone speaks to me loud enough the motor engine will stop also and than return upon their last word. Sometime sound drives the motor engine into the other ear and I feel a fluttering/vibration/rumbling sound in the left ear. If I shake my head back and forth quickly the noise will stop for a second while doing it.
Had so many tests and scans that don't show anything wrong. My hearing test are normal now. It is driving me insane. Can't eat or concentrate. Severe anxiety. Went to audiologist and see if I could have it masked but it is to loud. I can't believe I can still hear over this noise and distortion that is going on in my head. Some days are better than others and I think I may be getting better but it gets worse again. I have no dizziness at all. Some doctors told me meniere's disease or virus. I can't stand it anymore. Does anyone have any suggestions?
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I have suffered with a so called anxiety disorder now for about 6 years. It started when I was on the train home from university and all of a sudden I lost some of my vision, felt very light-headed, pins and needles all over and thought I might pass out. This was the first time I had ever felt like this and before this incident, I was a very outgoing and independent person. However, since this I have has 6 years of constant, 24/7, light-headedness with severe panic attacks. I cannot go out, I cannot be left alone so my life is basically non-existent.
I have had every medical check there is - bloods, MRI, EEG, ECG - and all sorts of differing meds - citalopram, sertraline, lamotrigine, pregabalin and the list continues. All tests have come back negative and none of the meds have made any difference really. I have also had many diagnoses - depression, GAD, depersonalisation disorder, agoraphobia and even an inner ear issue. I have had counselling, CBT, hypnotherapy and all haven't made a difference.
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Does anyone have personal experience of this problem? A 79-year-old friend with vascular dementia has been prescribed a whole series of atypical antipsychotic drugs over the past eight months, all with varying disastrous results. And yes - I know this is an off-label use of this group but they still get prescribed for dementia sufferers all over the western world.
She's been on mirtazapine 20mg once daily for about five years (with no apparent ill effects) and olanzapine 10 mg once a day for three months. Two months ago she very rapidly - over a few days - developed massive swelling of her left hand, with complete loss of use of the middle, ring and little fingers of that hand. An X-ray was inconclusive, mainly as she couldn't straighten the three affected fingers, and her doctor has been mystified by this ever since. He finally decided it was arthritis but it didn't look much like it to me, given the degree of swelling and deformity, and the speed with which it had come on. Anti-inflammatory drugs have been prescribed, but with minimal effect.
I visit her in her high-security psycho-geriatric unit at least three times a week. Last Tuesday (six days ago) she was still feeding herself perfectly normally with her right hand, once her food had been cut up for her. Three days later, she could no longer hold a spoon, fork or cup. Her right hand isn't swollen but I can clearly see the identical deformity in her last three fingers as in her left hand. All three fingers on both hands are curled up and twisted over each other.
After raising Cain at the home, I've managed to get her an emergency appointment at a rheumatology clinic tomorrow. In preparation for this, I've been doing some research over the weekend (and no, not on Wikipedia) and have discovered peripheral oedema (swelling) is a rare, but known, side-effect of olanzapine. I also found a long paper that had clearly been published in a learned journal on the subject of peripheral oedema with combined mirtazapine and olanzapine use. Unfortunately, it was in Turkish!
Has anyone suffered from this and how quickly did it improve once the olanzapine dosage was reduced? Also, how serious is the rebound psychosis when olanzapine is withdrawn?
She was originally on risperidone, but when that had to be tailed off because it left her with severe Parkinson-like symptoms, it left her way more psychotic than she'd been at the outset, with the result she stabbed another resident in the lovely retirement home she was living in. She's stayed that way ever since, hence the transfer to a grim high-security psychiatric unit, where she'll end her days. She was subsequently put on clozapine for a couple of months, which caused terrible athetotic movements - constant bobbing, weaving movements of head, jaw, tongue, arms and upper trunk - which made her life unbearable. I have to say, however, that when that was gradually withdrawn, I didn't notice any rebound psychosis.
I'm furious with myself for not researching this sooner, as I'm a former nurse, though neuro was my speciality. I'm even more furious with her idiot doctor for prescribing a med that isn't authorised for dementia, then failing to notice she was suffering from a known side-effect. Ditto the nursing staff at the home. When I mentioned this to the head nurse today, she blithely said she'd known all along it was a side-effect of olanzapine - though I suspect she was just covering up her ignorance.
My friend is beside herself, and it breaks my heart to see her like this. She knows there's something wrong, but doesn't understand what it is. She can't feed herself at all now. I tried her with a biscuit this afternoon and she couldn't even hold that. She's already dangerously underweight (BMI 17) and now she's refusing to let the staff feed her, as she's not used to that. I'm the only one who's allowed to feed her, albeit only a few mouthfuls, but I'm 71 myself and can't continue going in twice a day. In the meantime she's screaming and shouting all day and all night in anguish and sheer terror, and attacking everyone who goes near her. She tried to bite my face today.
Sometimes patients who've been on this class of drugs for long periods know much more about them than the professionals, which is why I'm posting here. Is this terrible condition likely to be a result of olanzapine (and possibly mirtazapine)? And can we expect severe rebound psychosis if her doctor tails it off? (Always assuming he even agrees to do that.) Also, does anyone have any experience of other recently-developed anti-psychotics that don't cause appalling side-effects of one kind or another? Though I have to say, from my own nursing experience, that I suspect there's no such animal.
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Was on 600mg Gabapentin 3 times a day for peripheral neuropathy to little effect. Was prescribed Amitriptyline, took 25mg for 3 days then 50mg for 5 days - replacing the 2 Gabapentin at night. Reduced Amitriptyline to 25mg after awful side effects. Took for 2 days with 300mg at night (in addition to the 600mg in morning and new GP said stop Amitriptyline and increase morning dose to 900 mg. Was OK for a while, but then feet and lower legs started severe pins and needles, difficult to walk. Disturbed sleep last night and feet and legs still bad. Is this withdrawal from Amitriptyline? How long will it last? GP rang and said gradually increase Gabapentin to 900 mg 3 times a day and if necessary go to 1200 mg 3 times a day.
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I had a PVD about 2 years ago, plus I've always had floaters, however, I just had a new floater and the doctor did laser eye surgery. I always have a great deal of anxiety and since this just happened right before I was to go out of the country on vacation I had a major panic attack and couldn't force myself to go. I was scared to be in a foreign land for fear something would happen. I don't want this to control my life, but now it has.
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I have peripheral neuropathy with severe edema from the waist down. My doctor will not give me water pills. Is there anything I can take homeopathically?
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I suffer from sciatica and peripheral neuropathy in the feet. Have tried to address both with diet restrictions and daily walks. Yet, the arthritis like pain in the back of my calfs and legs is getting intolerable.
My girlfriend has extensive lung problems and chronic resultant pain from coughing for hours on end - in the back and thorax areas. She was prescribed Gabapentin to relieve that pain. Works for her.
So she gave me two tabs to try for my problems. It was as though a miracle had taken place. No pain whatsoever. Almost no side effects - other than a slight feeling of increased relaxation.
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I'm late 5s,have had floaters since my 20s,back then they were small black or clear dots,fast forward,late fifties,now i've had pvds in both eyes,vitreous gel shrinks and pulls away from the back of the eye,now i have these clear to gauzy larger floaters,plus one large clumpy black one and I can't ignore them anymore. PVD is age related. I am just lucky enough to have these awful larger ones that can blur and obstruct vision. How does a person deal with it. Oh yes I also am starting to have dry eyes. Both also can cause hazy vision. Unless you've experienced it,no one else can relate
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I'm always having a eye stye. It always comes back after a week maybe 2 weeks. I already tried antibiotics such as natravox 500mg, erythromycin (sorry I don't know the spelling), terramycin. One ointment I always used when I feel that an eye stye is going to pop up the tobrex an eye ointment It may disappear a week but after that it goes back again.hope you could help me for prescriptions to try some other antibiotics/ointment for fast healing.
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I noticed a black floater in my eye a couple months ago and it seems to be fading now so i haven't been worried about it. But a couple weeks ago I noticed, very occasionally, mainly when i'm looking at a computer screen, this pinhole flash of light in the same eye as the floater. Again, its not often at all, some days i don't see it, and it's mainly when looking at a screen. I just saw the eye doctor not too long ago because i was having my first ocular migraine and they dilated me to make sure that's all it was and she said everything was fine at that point.
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I'm 35 years old and have worn glasses or contacts since I was 11.
I recently had a corneal topography done during pre-Lasik exam. There was some yellow in the right scan, indicating possible abnormality, despite "pristine" external corneas and d numbers.
Over the past 10 years (ages 25 to 35) my right eye went from a .5 to a 2.25 astigmatism, while my left eye went from 0 to .75. Between the yellow scan and the Rx history, I was told I have subclinical keratoconus.
My question is: is there any other explanation for this level of change in astigmatism over a 10-year period? For example, my work during the same time period has involved hours in front of computer screens every day, whereas before this was not the case.
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