Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Vision And Celiac


baldridgem

Recommended Posts

baldridgem Rookie

I just read on another forum that a person

gave up wheat and had an improvement in her

vision.

Has there been any research on the relation of

gluten and vision?

This is important to me as I have 2 sisters with

macular degeneration. If there is a relation I want

to send them the info.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



elisabet Contributor
I just read on another forum that a person

gave up wheat and had an improvement in her

vision.

Has there been any research on the relation of

gluten and vision?

This is important to me as I have 2 sisters with

macular degeneration. If there is a relation I want

to send them the info.

Yes there is a corelation,I read an article about it ,weeks ago,but don t have the link.

jerseyangel Proficient

That sounds interesting.

Judyin Philly Enthusiast
That sounds interesting.

I hope someone can locate the article. There are times my vision is perfectly clear and other times can't read street signs and my eye site is sooooo poor. Can't understand the 'changes' I'm so light sensitive now and wasn't before. notice posts about that here also.

love any info others can share.

Judy in Philly

nettiebeads Apprentice
I just read on another forum that a person

gave up wheat and had an improvement in her

vision.

Has there been any research on the relation of

gluten and vision?

This is important to me as I have 2 sisters with

macular degeneration. If there is a relation I want

to send them the info.

Man, that's interesting. My daughter's grandmother has that - said it's hereditary in that family. I'm really trying to steer my daughter into the wheat free life. Me with celiac disease and being half swedish, and then her dad's family is definitely from an Irish extraction and half of them complaining of stomach problems. She already has PCOS so I'm wondering if she's in for more problems.

  • 3 weeks later...
tiredofdoctors Enthusiast

If you have antigliadin antibodies and antiperkinje cells, not only do they cause destruction of the perkinje cells in the cerebellum of your brain, but they can also cause destruction of the perkinje cells in your retinas -- causing a whole host of problems. (I have double vision in the left eye, have started going color blind and night blind at 43). Amazing what that nasty gluten does, huh?

darlindeb25 Collaborator

Macular degeneration is hereditary. I work for an eye doctor and I asked him about it because my sweetie's mother has it. She is nearly blind now at 85. The doctor said there really is nothing you can do other then stay as healthy as you can, eat right, and have regular check-ups. He says the vitamins they advertise for it really do nothing--that was why I talked to him because Kev wanted to know what he thought about the vitamins that Paul Harvey advertises for macular degeneration. Deb


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



  • 2 weeks later...
Silver-naki Rookie

Hmmmm.... very interesting Post here on the Vision & Celiac~

I just had to go into "bifocals" this last Summer, and of course, there is always eye changes as a person ages... (so says the Optomotrist!) But in the last couple of months or so, I have noticed that my eyes seem to be getting bad again, & I'm having some trouble *seeing.* There's alot of "blur" and I don't focus as good as I was doing when I first got adjusted to my new bifocal eye-glasses.

Being gluten-free now, I haven't noticed much of a change, other than my eyes aren't cooperating for me like they should be..... I'll probably be going in for a check-up & eye Exam in the Spring again. Just to see if my eyes have changed any. I have heard that being "gluten-free," is suppose to definitely HELP the eyes. Gee, I hope so!!! {I'm still learning here!} I'll have to talk with my Eye Dr. about Celiac & see what his "take" is on it~

DonnaD Apprentice
Hmmmm.... very interesting Post here on the Vision & Celiac~

{I'm still learning here!} I'll have to talk with my Eye Dr. about Celiac & see what his "take" is on it~

I'm still learning too. It is very interesting that this topic caught my eye. Tomorrow we are taking our daughter to be checked for dyslexia because the optition doesn't know why her vision is blurred when she reads and wants to rule out dyslexia before referring her back to the Eye Clinic at the local hospital. What is the actual effect of the perkinje cells in your retinas -- causing a whole host of problems. Do you have any links you could share tiredofdoctors? or tests that could be run to rule it in/out??

I asked the optition about the possibility that the celiacs have visual problems but as usual with anyone in the medical profession she hadn't got a clue.

This gluten thing really is a can of worms isn't it?

gointribal Enthusiast

I know when I eat gluten it changes the way I see, I am a full time student and there I times I can't see three rows in front of me!

Judyin Philly Enthusiast
This gluten thing really is a can of worms isn't it?

You sure have that right Donna

I'd still have her ck'd for dyslexia however. Our son had that and is now 31 and we didn't even know what celiac disease was back then..He did have alot of allergies, milk shrimp cats mold pollen etc --He might even still have it -- I was dx'd 6 months ago so still all of these 'connections' are still new to me too.

Love to hear what the eye dr.s thoughts are.

Would love to see that article too.

Judy in PHilly

AileenWV Newbie
I hope someone can locate the article. There are times my vision is perfectly clear and other times can't read street signs and my eye site is sooooo poor. Can't understand the 'changes' I'm so light sensitive now and wasn't before. notice posts about that here also.

love any info others can share.

Judy in Philly

I can relate as my vision is good some days and other days is very poor. I blamed it on Laser surgery, but now that I have been diagnosed with celiac disease, maybe there is another reason. I hope the gluten free diet helps. I haven't been gluten free long enough to tell yet.

Let me know if your vision improves.

DonnaD Apprentice

We had the tests and she does have 'Moderate Dyslexia', "Short-term memory and phonics cause the most problems Significant reading difficulty. Very weak at Maths.

Strongest element is Verbal, and she's only just average in that. "

She is in the second highest stream for English and maths at (2 of 4) her school, god help the poor kids in 3 and 4! and it is one of the best schools in our area.

I was very shocked which surprised me. I was hoping I was wrong. Although I had read up and it and did a couple of on-line mini tests which did show problems, for years and years all her teachers (and a private english tutor) told me she absolutly did NOT have dyslexia, I was just comparing her to her exceptionally clever sister ( Straight As) and I was being unfair!

The weird thing is that she is much, much better being gluten-free. I hate to think what the results would have been in the summer when she had to eat Gluten for the biopsy. I do think that there must be some neurological damage to her brain/eyes though as reading past school reports shows a gradual decline in her grades and reading age conmpared to her actual age.

So now I must sprit my time between you lovely people and my 'new' friends on the Dyslexia forum :lol:

Donna

SurreyGirl Rookie
..., I haven't noticed much of a change, other than my eyes aren't cooperating for me like they should be.....

That's so much like me (and my mum before me..). I suspect that, as with other gluten damage, some may be permanent - especially if you consider Perkinje/neuro cells. But if it stays as it is - for me that's a hope.

I know of 2 cases affected by ataxia who also have eyesight damage, one of them has gone blind over the years. They have never been tested for gluten/celiac, but have signs of malabsorption which could be gluten related.

Silver-naki Rookie
That's so much like me (and my mum before me..). I suspect that, as with other gluten damage, some may be permanent - especially if you consider Perkinje/neuro cells. But if it stays as it is - for me that's a hope.

I know of 2 cases affected by ataxia who also have eyesight damage, one of them has gone blind over the years. They have never been tested for gluten/celiac, but have signs of malabsorption which could be gluten related.

With now going "gluten-free," I'm hoping for the best! :rolleyes: I've always had bad eye-sight, and with age, it is a known factor that your eyesight does get worse... all I can do is watch my diet and keep my Eye Exams up to date, & go from there~ I'm hoping there's no permanent "gluten" damage... gee, if so, then I'd be wearing "coke-bottle-SIZED" eye-glasses!!! :P:P:P

nettiebeads Apprentice
I'm hoping there's no permanent "gluten" damage... gee, if so, then I'd be wearing "coke-bottle-SIZED" eye-glasses!!! :P:P:P

Hey! I resemble that remark!!!! but I've had bad eyesight way before developing celiac. And the age thing isn't helping either. But so long as I can see a beefcake calendar or a SALE! sign I guess I won't worry.

:P

  • 1 month later...
Guest Robbin

I'm pretty new and I know this thread has been up awhile, but I am extremely upset since, along with all the other problems I've been having, I have been slowly losing my sight (over about 2 years) It's gotten really bad in the last year. I've always had bad eyes, but this is very blurred vision in one eye and double vision/blurred in the other. My "good" eye is now 20/60 with glasses and I am unable to drive at night because of night blindness, too. I only drive within a 6 mile radius of my home and I have to pay particular attention to the sun/weather. I have been to a total of 6 specialists. They are stumped. myopia of unknown cause. Some said "Well, as we age, our eyes aren't what they used to be" !@#*& ! I am only 45! My father-in-law was 93 when he died and had better eyesight than I did when I was 43! My mom has diabetes, high blood pressure, cataract surgery and has better eyesight than mine! I think I am stumbling onto so many answers, but I AM SO SCARED. I am going through so many different tests and health issues related to this disease that are so hard to handle. I think my next step would be to a neurologist? Does anyone have any experience with severe double vision in one eye or both? Sorry for the pity-party here.

TCA Contributor

I went for an eye exam in Jan. and my eyes had improved dramatically. I had a baby last April and the doctor said that it probably improved during pregnancy (although I didn't notice it then) I never considered the 4 mos. of the gluten-free diet could have done it at that time. I've worn glasses for 22 years and they had only gotten worse, even after the birth of my first child. It could have been the 2nd pregnancy, but now I wonder if it wasn't the diet. very interesting. :huh:

cgilsing Enthusiast

Very interesting! I've always had problems with my eyes! My vision is something like 20/140 and has been since I was about 8. They put me in hard contacts when I was 10 to try to stop the rapid change in my vision. It worked. I haven't had any rapid changes since then. However I have night vision problems, blurred vision that comes and goes, and very dry eyes. My eye doctor sent me to a speicalist about a year ago for a thyroid test because my eyes were so dry. He said if I was 60 he wouldn't be that alarmed, but since I'm 25 he felt it was pretty unusual. My thyroid was fine, and I haven't been back to my eye doctor since then so I still don't know what that's all about.

Guest Robbin

This is so interesting to me and thanks for the info everyone. I can't get a correction in my right eye, but I am hoping the diet will slow the progression in my left so I can at least drive around town. The trouble is distortion more than anything. I can't read signs, which is annoying, but I see what problems people who don't know the language and are illerate go through. I just had an exam with a new dr. that came highly recommended and he is going to refer me to an eye surgeon. The retina specialist is stumped because the retina is ok. I have a gazillion floaters. Does anyone have tons of floaters, too? I've had them since childhood, but I also believe I've had celiac since childhood, too. I am so hoping the gluten-free diet works some miracle for this too. The D and the rash are gone after 20 yrs, so I consider that pretty amazing anyway. Thanks again, you guys are the best.

mouse Enthusiast

I have been having vision problems for the last 2 1/2 years. They could not find anything wrong. Then late last summer it got worse and I saw the optomologist and he said it was dry eye related to my Morphia Scleroderma. Then 3 weeks ago my blurred vision got VERY WORSE and the optomolgist still said it was related to the scleroderma. Today I saw my Morphia Scleroderma doctor and it is not that. He said I had to see a Neuro Optomolgist NOW. I have an appointment tomorrow morning with one. I just hope they can stop whatever is happening before I can't drive. I no longer drive anywhere that is not close and familiar. I can't read signs anymore at all, nor see my husband's face when he is 8 to 10 feet away from me. I also have to see a Rheumotologist for my cold hands and feet. He also said that he wants me into one this week. He thinks I have some neuropathy damage and it is progressing too fast. One auto-immune disease (Celiac) begets another (Morphia Scleroderma) and begets another and another. So far I am handling this well. I will wait to see what these additional doctors have to say before I fall apart. Oh, today's doctor also said that Celiac itself does not cause the vision problems, but that the Malapsorption does. And that would probably depend on how long and genetics. I hope I got all this information right.

Guest Robbin
I have been having vision problems for the last 2 1/2 years. They could not find anything wrong. Then late last summer it got worse and I saw the optomologist and he said it was dry eye related to my Morphia Scleroderma. Then 3 weeks ago my blurred vision got VERY WORSE and the optomolgist still said it was related to the scleroderma. Today I saw my Morphia Scleroderma doctor and it is not that. He said I had to see a Neuro Optomolgist NOW. I have an appointment tomorrow morning with one. I just hope they can stop whatever is happening before I can't drive. I no longer drive anywhere that is not close and familiar. I can't read signs anymore at all, nor see my husband's face when he is 8 to 10 feet away from me. I also have to see a Rheumotologist for my cold hands and feet. He also said that he wants me into one this week. He thinks I have some neuropathy damage and it is progressing too fast. One auto-immune disease (Celiac) begets another (Morphia Scleroderma) and begets another and another. So far I am handling this well. I will wait to see what these additional doctors have to say before I fall apart. Oh, today's doctor also said that Celiac itself does not cause the vision problems, but that the Malapsorption does. And that would probably depend on how long and genetics. I hope I got all this information right.

Armetta, OMG, you sound exactly like me. What is an neuro-optomolgist? I really hope you keep posting on your condition. Facing a future of not being able to drive is sooooo upsetting, I know. I am scared of harming myself or others it is so bad. I live in an area that doesn't have a lot of physicians, and since my dear husband has to take off work to drive me everywhere, it is frustrating. Went all the way to Baltimore to a so-called specialist at a so-called-world-class institution and got no answers-was made to feel like I was a waste of time. He said I just needed new glasses, measured my eyes and got mad acting when I said I couldn't see the chart with the lenses he had up. A dr. I just saw last week (recommended by a friend) said that the measurements on the machines are not right because I have major distortion, so he is getting all my records and trying to find someone to help me. Keep me in your prayers--you are in mine too. Keep me posted!! I may have to fly out to AZ to get help if your dr. helps you. I have friends in Tucson.

mouse Enthusiast

I saw the Neuro-Opthamolgist today. It was such a long drive, but well worth it. Of course my hubby had to drive and then twiddle his thumbs eating breakfast somewhere (poor baby). He really does not mind-thank goodness. But, the news was very good. After a couple hours of many different tests, the majority that I had never had before, the doctor gave me his expert opinion. I need to change my prescription in my glasses and I have a severe case of dry eye. I am to stay on the RX for that and also use the OTC ones more then 4 times a day. I am especially to use the OTC drops before getting on the computer or reading a book. It will take time for the RX one to work. He also took photos' of the eyes for future reference, just in case I end of with a Neuro problem with them due to the Celiac. But, he really did not think this would happen. A Neuro-Opthamologist also looks behind the eye at the nerves to see if there is neurological damage. I was in his office three hours and only about a half hour was spent filling out forms and waiting. The rest was with tests and him. I have just had a regular opthamolgist exam and he said that there was no need to change my glasses as the change was so slight. After all the tests, this doctor then gave me a regular exam and I could not believe how different my vision was when he flipped all those eye thingies. I was really scared that I was going to go blind. This was such wonderful news.

I hope this helps you Robbin. I saw this doctor in Phoenix, which would be about 2 hours North of Tucson. I live in the very East Valley and we drove about 70 minutes. If you do decide you want the name of this doctor PM me. I was really impressed.

Guest Robbin

Congratulations! I am so glad you have been helped. Not many things as scary as blindness, in my opinion. I have had 4 different optomotrists, a retina specialist, and an opthalmologist check this out in the past 1 1/2 -2 years and was giving up until my good eye started getting so much worse, so I hope this guy I saw finds a way to help me. I am still in the "waiting for records to be sent" mode. A trip to AZ would be a good excuse to see my dear friends there too, so if this dr. doesn't pan out, I may visit your guy. Something like this just doesn't "happen". I am afraid it may be from long term misdiagnosed celiac. If so, gluten free will halt it, I hope. Was your dr. experienced with celiac?Thanks-God bless! Robbin

zakismom Newbie

I also work in the optical field and there is definate proof that lutein and lycopene can help prevent some eye diseases or make their symptoms more bearable. I'm thinking that since we have malabsorption issues we may have missed a lot of the nutrients that are eyes need to stay healthy. (Unfortunately for macular degeneration, after a certain point there is nothing you can do but in the beginning or if it's in your family-eat spinach!)

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,549
    • Most Online (within 30 mins)
      7,748

    Blough
    Newest Member
    Blough
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.