• Ads by Google:
     




    Get email alerts Subscribe to Celiac.com's FREE weekly eNewsletter

    Ads by Google:



       Get email alertsSubscribe to Celiac.com's FREE weekly eNewsletter

  • Announcements

    • admin

      Frequently Asked Questions About Celiac Disease   09/30/2015

      This Celiac.com FAQ on celiac disease will guide you to all of the basic information you will need to know about the disease, its diagnosis, testing methods, a gluten-free diet, etc.   Subscribe to Celiac.com's FREE weekly eNewsletter   What are the major symptoms of celiac disease? Celiac Disease Symptoms What testing is available for celiac disease? - list blood tests, endo with biopsy, genetic test and enterolab (not diagnostic) Celiac Disease Screening Interpretation of Celiac Disease Blood Test Results Can I be tested even though I am eating gluten free? How long must gluten be taken for the serological tests to be meaningful? The Gluten-Free Diet 101 - A Beginner's Guide to Going Gluten-Free Is celiac inherited? Should my children be tested? Ten Facts About Celiac Disease Genetic Testing Is there a link between celiac and other autoimmune diseases? Celiac Disease Research: Associated Diseases and Disorders Is there a list of gluten foods to avoid? Unsafe Gluten-Free Food List (Unsafe Ingredients) Is there a list of gluten free foods? Safe Gluten-Free Food List (Safe Ingredients) Gluten-Free Alcoholic Beverages Distilled Spirits (Grain Alcohols) and Vinegar: Are they Gluten-Free? Where does gluten hide? Additional Things to Beware of to Maintain a 100% Gluten-Free Diet What if my doctor won't listen to me? An Open Letter to Skeptical Health Care Practitioners Gluten-Free recipes: Gluten-Free Recipes

Vision
0

Rate this topic

24 posts in this topic

Recommended Posts

Has anyone had problems with their vision? I have never noticed this before I was diagnosed, but since my diagnosis in feb 2006 my eyes have been doing weird things. Today, I went to my children's conferences at the high school. I went into the bathroom and when I was washing my hands, I couldn't focus on the mirror in front of me. It felt weird. I walked toward the door and it was only then that I realized that what I thought was the mirror was an opening in the wall. The mirror was really by the door several feet away. I had the same experience earlier in the week with a mirror. I felt like I had no depth perception. Isn't this weird?

  • Upvote 1

Share this post


Link to post
Share on other sites
Ads by Google:
Ads by Google:


I went gluten-free in Sept. I've worn glasses for 22 years and for the first time ever my Rx improved in Jan. Since then I have heard that gluten can cause damage that leads to needing glasses. My Rx is about 1/2 what it was. I was amazed as was the doc!

  • Upvote 2

Share this post


Link to post
Share on other sites

In the past, and still on occassion, I have had opthamolic (sp?) migraines. I never got the headaches associated with "normal" migraines (until much later). Instead my vision was impaired.

This is about the time my symptoms related to celiacs first started rearing their ugly head, but I didn't suspect anything yet.

Sometimes my peripheral vision would just go on me-it would feel almost as if invisible blinders had just been put on me. Other times, portions of my frontal vision would go. Scary - especially as I was driving one day and realized I couldn't see all of the car in front of me.......threw my distance and depth perception all off.

My eye doctor said that they could often be brought on by "stimulants" like......chocolate, nicotine, some soft cheeses(!), and caffeine.

I was, at the time, a college student surviving on sweets, a smoker at the time, and addicted to Dr. Pepper (Still am addicted to that vice. :lol: ) and I could not trace the incidents to any of those things b/c I used them all the time.

I wonder now if it was celiac disease, and I just didn't know any better. I still have them every so often. I haven't sat down to track yet if it's connected to glutenings.

Of course, with two grandmother's with glaucoma and cataracts I am very acutely aware of changes in my vision. Ask you eye doc about opth. migraines. I'd be curious to see if that's what you're experiencing and if they're linked to celiac disease.

Good luck!

Share this post


Link to post
Share on other sites

I had something similar (migraines with no or little pain, just vision disturbances) starting when I was pregnant with my first child. It coincided with preeclampsia in my case (dangerously high blood pressure); it later returned a month after the birth (but without the high blood pressure)--my doctor said that at that point it was caused by hormone changes.

Are you on birth control pills? That might have something to do with it. You also might invest in an inexpensive blood pressure monitor and check out your own blood pressure, just so you can rule things out.

Can you tell if you are using both eyes together, or are you using one primarily and suppressing the vision in the other? You can check this by covering one eye, looking at an object, and then open the other eye and then cover the eye that was doing the looking. Then try this with the other eye. If everything is normal, you shouldn't feel the second eye move as it focuses. If it does, that means you are doing all your focussing with one eye (the other is either just getting peripheral vision or the brain is suppressing theimage so you don't get double vision.

Scary, isn't it? I hope you find some answers.

Share this post


Link to post
Share on other sites

I was dx'd with optic neuritis and they thought MS, but now gluten free it has all gone away!

  • Upvote 1

Share this post


Link to post
Share on other sites
Ads by Google:


Thanks for all of your advice. My blood pressure is usually pretty good. I am on estrogen as I had a hysterectomy 3 yrs ago. I am planning to see my dr. in a few weeks for my yearly, so I'll ask her then about the vision thing.

Share this post


Link to post
Share on other sites

I have had alot of problems with my vision too. (Boy, after you've read all my recent posts you'd think I was a serious mess! :lol:) I have problems with blurry and cloudy vision and also peripheral problems. I have been running into things that I swear was further away than it really was. I grew up having numerous migranes too. My eyesight is getting worse it seems but then again I have only been on the diet 2 months so I guess my eyes haven't had time to straighten out yet. (Plus I have been contaminated alot of times in the 2 months too.) Good luck to you!

  • Upvote 1

Share this post


Link to post
Share on other sites


Ads by Google:


my vision always gets screwed up when my thyroid gets out of whack, you might want to check that out to see if you need thyroind meds.

  • Upvote 1

Share this post


Link to post
Share on other sites

in a rush sorry,whitbal!

My daughter had optical migranes with aura on gluten and was dx dyslexic just after her celiac dx in Nov 05.(words blurry on page hated reading, some ADHA symptoms).

Post DX, and on 2 x 100mg fish oil twice a day and berocca (high dose multi vit) Oxford University Dyslexia research unit found she is no longer dyslexic, reading age up 2 years in 5 months, but she did have convergence insufficiency (google it) had eye exercises for 6 weeks, now cured, still has a contrast and depth perception problem and has BRIGHT YELLOW glasses for reading and when tired, she can then see the 'numbers in the coloured spots' on the charts, amazing. She is reading for fun now. They have done a lot of research into the link of diet (esp fish EFA oils and B vits) on vision and attention (being celiac vital vits and minerals are malabsorbed).

I have also found myself that what I though were 'tired eyes' looking at the computer etc and driving at night is 80% better gluten-free. I don't shut one eye anymore when reading at night!

Hope this gives you some ideas to try,

D

Share this post


Link to post
Share on other sites
I have had alot of problems with my vision too. (Boy, after you've read all my recent posts you'd think I was a serious mess! :lol:) I have problems with blurry and cloudy vision and also peripheral problems. I have been running into things that I swear was further away than it really was. I grew up having numerous migranes too. My eyesight is getting worse it seems but then again I have only been on the diet 2 months so I guess my eyes haven't had time to straighten out yet. (Plus I have been contaminated alot of times in the 2 months too.) Good luck to you!

I have had problems with peripheral vison too. I can no longer use my glasses. I try to use my bifocals, but can't use them with my computer. My vision has been worse since this diet. Not sure of what is going on. good luck to you also. We've got a long road ahead of us. Tara

Share this post


Link to post
Share on other sites


Ads by Google:


. I don't shut one eye anymore when reading at night!

Hope this gives you some ideas to try,

D

That's fascinating, DonnaD! I have ALWAYS shut one eye when reading--but I never connected it to gluten before. I did all sorts of eye exercises (for either strabismus or ambliyopia, depending on which doctor you believed) as a child, but they never worked. Come to think of it, I haven't had time to read much lately--I'll have to check it out now that I'm off gluten!

  • Upvote 1

Share this post


Link to post
Share on other sites

Hi,

Funny you should mention this. Since have problems with gluten, my eyesight seems to worsen. Sometimes it just feels like there is something over one of my eyes that needs to be rubbed away (a slight blurring). I do wear glasses for reading, but can still read without them.... but there are days, since having this gluten problem, that I can't read unless I have plenty of light and my glasses on.

Steve

  • Upvote 1

Share this post


Link to post
Share on other sites

I feel like my night vision isn't what it should be, but I went to the eye doctor and they told me to be a pilot because my vision is better than 20/20 :blink:

Like, a lot better. Read the bottom line of the chart with one eye better.

Doesn't mean I don't get eye strain though. Since doing this gluten challenge my eyes are itchy all of the time, though.

Share this post


Link to post
Share on other sites

I have visual migraines (always preceding the actual headaches, which I can sometimes head off if I immediately lie down in a dark room) & also notice that my eyes are extremely sensitive to bright light. Also, I find that my eyes will sometimes feel very "sludgy" & slow to focus (sort of as they do when I first wake up) during the day for no apparent reason. Who knows, maybe that too is Celiac-related!

Curiouser & curiouser!

Leah

Share this post


Link to post
Share on other sites

Went to the eye doctor, nothing wrong I have 20/20 eye sight, but my eyes do the weirdest things. I don't know if I'm blacking out, but, a lot of the times my sight will nearly completely black, I can only see about around the middle of my sight, I have no idea what this is but when I'm not dealing with that, my eye sight is vivid as ever!

-Ash

  • Upvote 1

Share this post


Link to post
Share on other sites


Ads by Google:


I have also had problems with my eyes, I have noticed especially in the early to mid morning. Feels like I cannot focus and when looking into the mirror it's as if my eyes aren't dilating. Could this be related to a rxn to a breakfast food? Has anyone else had a similar vision prob.?

Share this post


Link to post
Share on other sites

About 3 years ago I had a short episode where it seemed like I was looking through a black and white calidascope. It only lasted about 20 minutes. When I saw my eye dr. I told her, as I was on a medication that can cause eye problems (due to arthritis). She said is was a "visual migraine". About a year ago, I had another episode like this, so thought nothing of it until my left arm and nose and lips went numb. I ended up at the ER (had to rule out stroke and heart attack) and was diagnosed with a migraine again. I had to follow up with a nuerologist. He recommended getting off birth control, which I did. This summer they found my celiac, so I have been gluten-free since August. In October I had a bad dining experience where I was very ill right after, so I know I had gluten. One week to the day later, I had another "visual migraine" with the numbness. I called the neurologist as I didn't automatically equate it to the gluten. Once he learned of my celiac diagnosis, he accused me of cheating on the diet. It was only then I made the connection with the gluten exposure. My visual migraines have been as simple as the black dots that float, to feeling like I was looking through a distorted window. "Tunnel vision" is often part of this as well. Hopefully this gives you some ideas of what to check out with your physicians.

Share this post


Link to post
Share on other sites

Has anyone had problems with their vision? I have never noticed this before I was diagnosed, but since my diagnosis in feb 2006 my eyes have been doing weird things. Today, I went to my children's conferences at the high school. I went into the bathroom and when I was washing my hands, I couldn't focus on the mirror in front of me. It felt weird. I walked toward the door and it was only then that I realized that what I thought was the mirror was an opening in the wall. The mirror was really by the door several feet away. I had the same experience earlier in the week with a mirror. I felt like I had no depth perception. Isn't this weird?

One of my problems before going gluten free was my night vision getting really bad. Add rain to it and I couldn't drive with glasses on. My Mom was with me one night and she had to finish driving us home. Since going gluten free my eyes have improved a great deal. I don't even need glasses to drive at night now.

Share this post


Link to post
Share on other sites

I was dx'd with optic neuritis and they thought MS, but now gluten free it has all gone away!

This is where I'm at. I was diagnosed over 8 years ago with MS. Had optic neuritis th first year, then nothing. I got diagnosed with Celiac last year but am positive that I have had it since I was a teenager(which was before the MS). I just had my second MRI and they phoned to say they dint find anything. So I am wondering if I don't have MS and maybe it was the Celiac that resembled MS symptoms. The biggest problem I have is when I went to my doc questioning the MS diagnoses, she said there was no question whether or not it was ms, even after I asked her about the connection between the two. So when I go now, she is probably going to say the same thing.......I wish there was a Celiac specialist around here that I could talked to......This is the next best thing..

Share this post


Link to post
Share on other sites

This is where I'm at. I was diagnosed over 8 years ago with MS. Had optic neuritis th first year, then nothing. I got diagnosed with Celiac last year but am positive that I have had it since I was a teenager(which was before the MS). I just had my second MRI and they phoned to say they dint find anything. So I am wondering if I don't have MS and maybe it was the Celiac that resembled MS symptoms. The biggest problem I have is when I went to my doc questioning the MS diagnoses, she said there was no question whether or not it was ms, even after I asked her about the connection between the two. So when I go now, she is probably going to say the same thing.......I wish there was a Celiac specialist around here that I could talked to......This is the next best thing..

How were you diagnosed with MS? Did you have a spinal tap that was positive for it or did they diagnose based on symptoms or a previous MRI that showed white lesions? If you were diagnosed with a positive spinal tap with MS then as far as I know you unfortunately have MS. MS isn't always a disease that has constant symptoms though so perhaps it could be in an 'off phase' after the eye symptoms resolved. I don't know I am far from an expert with MS.

There is a neurological celiac form that is called gluten ataxia. That can make you very off balance. That can cause lesions and symptoms that are similiar to MS but the spinal fluid will be clear of the debris that comes with MS.

Doctors unfortunately don't know a great deal usually about celiac's impact on the brain. There is quite a bit of stuff out there on everything from gluten ataxia to glutens relationship to some mental illnesses but most doctors have no knowledge of this. Sometimes printing out peer reviewed studies from places like the NIH can help them understand why your questioning.

Share this post


Link to post
Share on other sites


Ads by Google:


One of my vry first signs two years ago was vision problems. Went to eye doc and nothing was wrong with my eyes. That didn't explain the blurry vision and sometimes double vision. At it's worst I was having vertigo, just real weird stuff happening like a white wall behind a person would make it hard for me to see the person, going down a escalator my eyes seemed to focus on the lines in the steps which were very bright. And my depth perception was off so when I would drive I felt like I was squeezed between two lines and it felt like I could easy go over the line. I actually ended up hitting a curb at a corner at a fairly good speed and flattened a tire.

Share this post


Link to post
Share on other sites

I've also had an experience where my eyesight improved.. I went to the eye doctor, and he exclaimed that my prescription went down and what did I do?! Well, the only thing I changed was going on the gluten free diet! :D

Share this post


Link to post
Share on other sites

Went to the eye doctor, nothing wrong I have 20/20 eye sight, but my eyes do the weirdest things. I don't know if I'm blacking out, but, a lot of the times my sight will nearly completely black, I can only see about around the middle of my sight, I have no idea what this is but when I'm not dealing with that, my eye sight is vivid as ever!

-Ash

Please know that I have no medical experience or knowledge!! I do, however, have 2 relatives with macular degeneration, and that's how they explain what their vision is like.

Also, when I had ovarian cysts, I had migraines with auras, then my vision would do something similar to yours. I hope neither of these is your problem!! Hope everything readjusts for you soon!

Share this post


Link to post
Share on other sites

I had optic neuritis after the birth of my son 6 years ago. I had an MRI and 2 follow on MRIs in the next 2 years with no signs of MS. The doctor indicated that 20% of the time there is no known reason and I likely fell into that category. I have just been diagnosed with celiac in the last 2 months and my gut tells me that it was the celiac that caused the eye problems. I'm relieved because I felt like I had an MS cloud hanging over my head for the last several years. I'm feeling so much better overall on the gluten free diet and it's nice to have answers to several unexplained symptoms.

Share this post


Link to post
Share on other sites

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

0

  • Forum Statistics

    • Total Topics
      108,142
    • Total Posts
      939,890
  • Member Statistics

    • Total Members
      66,131
    • Most Online
      3,093

    Newest Member
    Larryx
    Joined
  • Popular Now

  • Topics

  • Posts

    • My son is 13 and we have been dealing with his unusual issues for years. By 3rd grade, he was The Hulk, breaking things, punching holes in walls and raging. He had depression, anxiety and panic attacks. His skin would have rashes or turn bright red and i didn't understand why (now i know it's salicylic acid added to conditioner, sunscreen, lotion, ect). We realized that dyes were a problem and cut those out. Little by little, we removed sulfur, sulfites, preservatives, salicylates (aspirin-we assume he will be allergic to this but he has never had it and we won't ever test it, most fruits, spices, veggies and honey), nitrates, soy sauce and many more. He lived on an all home made, special diet and he was better but not well. (We did the Feingold and Failsafe Diet but that wasn't enough). He was diagnosed with hypersensitivity to medication by 5th grade (tried anti-anxiety meds-big mistake). Consecutive doses of anything would get stuck in his body and then the real fun started, full body rash, suicidal thoughts, vomiting and my least favorite-hallucinations. He was in the ER for a fall from a tree and they gave ibuprofen and Vicodin. Within 30 minutes the rash spread up and down his whole body (including under the damn cast). The worst night of my life was trying to keep him from breaking his own cast off and talking him down from trying to hurt himself.                                                                                                                                                                                                                                                             We tested my son for everything and anything, hormones, vitamin deficiency (later found out they don't test for nearly enough to really know) and thyroid. Everything was normal but a mildly low vitamin D level. He was very unhealthy, he was sick a LOT, allergies were bad, asthma and he developed food intolerances out of nowhere. We did a gluten/dairy free diet (because his sister is gluten/dairy free) but it made no difference and his diet was already so restricted. We did a year long food journal and also found an issue with pork, apples, citrus fruit, cinnamon, ect.  I researched my kid like it was my job. We tried many vitamins and supplements and he had bad reactions to many of them. I finally found a man with several of the same gene mutations (we tested with 23andme.com) who's Dr. thought it was a PST-Pathway issue. We decided to try the protocol of vitamins, supplements and amino acids to see if it made any difference and OMG, what a difference. At this point, we didn't have a pediatrician that actually listened so I asked several doctors about the specific vitamin/minerals/amino acids and kept all the does to a child size dose.  We had always used epsom salts as a response to a reaction in something, not as a preventative measure. We now soak his feet twice a day in Epsom salt water (or in the bath), it gives him a form of sulfur that his body was missing and now he can eat anything he wants (except soy sauce but we'll gladly leave that out). He takes molybdenum everyday with magnesium/calcium and vitamin D3 (and when we stop that, panic attacks come back. Weekly he takes milk thistle (we tried L-Glycine but too much gave him terrible insomnia (like 3 days of barely any sleep) and milk thistle works just as well to keep his liver open and working it's best), B vitamins, Cod liver oil capsules with Vitamins A and D and liquid Zinc.  His personality changed on the L-Glycine in a more outgoing way but then in a manic, not himself way so that scared us. Since the supplements started (6 months ago), his anxiety and depression is gone (and it was really controlling how we lived). He would never talk to people before...he was diagnosed with selective mutism but we felt that was incorrect and he was just very shy. He never liked talking with adults. Now, there is no problem, he is not super chatty with everyone but all he adults in our family noticed immediately. He is ready to stop home schooling and start high school next year. He has become a responsible, sweet, calm and caring child. No more daily fights, no more holes in the walls, no more rage. Our daughter has anorexia and we have been very busy dealing with her behaviors and missed the daily vitamins on occasion for several days....old son comes raging back. It doesn't take too long to figure out the mistake and gets him back where he needs to be. We did some genetic testing with a neurologist who specializes in metabolic function and while he tested for some helpful issues relating to hypersensitivity to medication, I still got the impression that he thought it was a placebo effect. We have burned through many therapists, pediatricians, a neuropsychologist, a psychiatrist, a gastroenterologist and possibly this neurologist. I hate not being taken seriously because while they may not agree with my ideas, they have nothing to offer in return.   
    • Yep no fruit, juice, sugar, or grains like oatmeal. The sugars glucose, fructose etc. Are common causes of flares in some. Sugar free fiber like nuts, but butters, cocanibs seem to be great for me. Keto diet sugar free high fat, mostly over cooked to mush or blended works great for me......heck as a baker I had to invent low carb, grain free, starch free bread. Sorta lead to a god like revelation and business took off with diabetics and my bakery.
    • Gastritis was my initial diagnoses before finding out I had celiac. The pains from the gastritis were terrible. I had to wake up in the middle of the night to eat cause I felt nauseous. The Doc prescribed me omeprozole and antacids. I took the meds for about a week but I cured it mostly by not drinking and eliminated caffeine intake. Alcohol was one of the main causes for mine 
    • The UC is a whole different beast. I’ve been eliminating tons of food. Meat is definitely good to me. I can eat all the steak, chicken, and pork without problems. I agree that paleo would be great for me. I’m gonna look more into their recipes.  Have you had any problems with fruits and veggies causing flare ups? I make smoothies with mixed berries, banana, gluten free oatmeal, spinach, and a splash of juice. It seems to be a cause. Maybe it’s the high fiber? I’m not sure. That and caffeine. I’m having a hard time eliminating caffeine though  
    • Pain wise a glutening celiac gets me more central gut pain and much worse with sharpness, urge to vomit, gurgles etc. UC is more along the the outside edges of your abdomen from the sides, lower area around the belt line, and upper area right under the rib cage, and is more of a boat and pleasure pain like your intestines are huge feeling.  UC triggers alot more gas, and makes you want to lie down I get the urge to massage and press on the pressure areas as it seems to help.
      Timing wise Celiac glutening I notice within 20-60mins and main vomiting starts in 1-3hours after eating it. UC flare you get it like 4-18hours or later depending on transit time of your food. A glutening will normally result in both a celiac reaction and a later UC reaction. For me a gluten CC or consumption issue also causes neurological symptoms, this is not true for some people but for me I also have a gluten ataxia, so the anxiety, panic, fog, mind looping, numb hands, loss of coordination or straight up motor loss is definite sign for me. Others will have to keep track with a food diary to nail down there own as every person can have a slightly different reaction.

      I also find with UC I do not directly vomit, Sometimes with UC it can trigger constipation and if not remedied in 12-24 hours leads to m system backing up and vomiting. Celiac can also cause me constipation but there is a slight difference in where it seems to get stuck at first. Hard to explain but you can sort of feel it. Also I find a gluten celiac response will result in a week or more of constipation issues. Starting mid section then moving to the outside gut area and  but some people do not get these and get D instead. So this is not very reliable.

      UC flare ups for me with my damage also always have bloody stools, worse flare ups its not just streaks but clots. Red and Dark red show it is in the large intestines. If you get tar like black  and red it is either a sign it is way back in the large intestine or in the stomach or small intestine. This makes my Anemia SOO much worse. Imagine how you feel with the loss of blood coupled with inability to efficiently absorb nutrients like iron and magnesium

      Thing to recall is UC is mostly the large intestine while celiac is mostly the small, so symptoms and trying to get the feeling of where the problem is can help.  Also if you get a glutening expect to have the UC flare up right after the celiac flare up.

      NOTE it is hard for me to say still, on the exact details and clarity, it has been since june of last year that I had a major gluten consumption issue. UC I get more regular but without the direct comparison in a while my memory is a bit iffy. Just trying to recall those exact pains and feelings from that last time. Also UC seems to wax and wane in and out while almost always being present for months in the background you just feel a bit off in the gut. SO many triggers, I felt that for years I swear til I went to this keto diet and dropped all fruit, sugar, carbs, and grains. Could have been the anemia, but I think it was more of a combination of the inflammation, bleeding, gas, and just being uncomfortable.
  • Upcoming Events