Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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 Issues


Cathylinds

Recommended Posts

Cathylinds Rookie

Has anyone experienced headaches and kalidescope vision after going gluten and dairy free.  I was diagnosed with celiac at the end of June and the headaches and vision problems started about three weeks ago 


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



Celiac.com Sponsor (A8-M):



cristiana Veteran

Hi Cathylinds

Have you suffered from any type of migraine before?

I seem to have had all sorts through the years.  Pain and nausea, often starting in my neck, then auras both eyes, and after going gluten free a rapid improvement, only to get what they think is an aura in my right eye when I peer at black and white print which started after about a year of being gluten free.  Oh - and I'm now getting the pain and nausea ones back that start in my neck (which I attribute to hormones/peri.)  

 

 

 

 

Cathylinds Rookie

I had vision migranes once or twice I had trouble seeing far away but now I can’t see close up 

cristiana Veteran

Yes - seeing close up is what brings on my one eye aura.  I went to the doctors and the opticians and they seemed to think that as I am predisposed to migraines it was just another type.  I've had a few MRIs in the past but they didn't offer me one on this occasion.  Perhaps they felt as I was a migraine veteran I didn't need to have further tests, but as a hypochondriac as much as I hate seeing doctors and having tests I'd almost rather they had as I feel there is a bit of uncertainty about my latest diagnosis.  That said migraines are incredibly common.

How long do the visual disturbances last for?  I think auras typically last about 20 minutes don't they?

I think in your position I'd make an appointment with an optician or doctor and see what they think.  

tessa25 Rising Star

I used to get migraines regularly. They stopped as soon as I started taking magnesium.

 

cristiana Veteran
17 hours ago, tessa25 said:

I used to get migraines regularly. They stopped as soon as I started taking magnesium.

 

That's a great tip.  I've stopped taking it so I'll give it another try!

Posterboy Mentor

Cristiana,

Here is the research on Magnesium.

https://www.ncbi.nlm.nih.gov/pubmed/22426836

It is best taken ahead of a migraine. ..it doesn't work (as) well for acute cases.

But B-2 Riboflavin might.  It has a high degree of correlation to migraines and why taking a B-complex should help too!

A B-complex (B6,B12, Folic Acid) could also help your Homocysteine levels which can lead to eye problems too. . . especially the B-12.

This research summarizes these findings well.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359851/

Here is a good livestrong article on B-12 possible connection's to migraines.

https://www.livestrong.com/article/268141-b12-migraines/

I hope this is helpful but it is not medical advice.

2 Timothy 2: 7 “Consider what I say; and the Lord give thee understanding in all things” this included.

Posterboy by the grace of God,

 


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



Celiac.com Sponsor (A8-M):



cristiana Veteran

Thanks so much, Posterboy!

 

tessa25 Rising Star

To be clear. I stopped getting migraines when I started taking magnesium daily.

posterboy and ennis are the experts on how much to take.

Posterboy Mentor

cristiana and tessa25,

Here is a good thread on the many benefits and the best form and frequency to take Magnesium.

Never double (2x) up a dose of Magnesium Citrate (to catch up on a tablet/capsule) if you forgot to take it at breakfast/lunch etc.)) or take it on an empty stomach and you should be fine.

Taking the more expensive Magnesium Glycinate will not flush the way Magnesium Citrate can.

Space it out either morning and evening (2x) or with each meal which ever is most convenient.

It really helps fatigue, cramps, produces vivid dreams and a steady movement for most people especially as the Magnesium Citrate form with meals.

Dreams will begin to become vivid too you in the first couple weeks after starting Magnesium Citrate/Glycinate a sign you are taking it a high enough dose to actively effect your body in a positive way.

I hope this is  helpful but it not medical advise.

As always “Consider what I say; and the Lord give thee understanding in all things” 2 Timothy 2: 7, this included.

How else can we learn if we don't consider what others have to say?

I learn soooooooo much by what others share and I truly hope this is helpful.

Posterboy by the grace of God,

  • 3 weeks later...
Teliac92 Newbie

Thank you for responding with this information. 

I was taking 500mg of magnesium for about a week but it did not help with my headaches. Is magnesium citrate different than magnesium? 

tessa25 Rising Star

I took magnesium oxide, because that's the only kind I can take. But I wouldn't recommend trying that route. Probably magnesium deficiency isn't your reason for headaches. It worked quickly for me.

  • 1 year later...
RD13 Rookie
(edited)

Hi - I have been diagnosed with celiac disease two months ago. I too am suffering from strange vision issues -- things don't seem solid to me sometimes. I have been to a few eye doctors, and most of them are of an opinion that I suffer from dry eyes. Is that common in celiac disease? I have been putting the recommended eye drops but have not felt any significant improvement tbh.

Edited by RD13
cyclinglady Grand Master
59 minutes ago, RD13 said:

Hi - I have been diagnosed with celiac disease two months ago. I too am suffering from strange vision issues -- things don't seem solid to me sometimes. I have been to a few eye doctors, and most of them are of an opinion that I suffer from dry eyes. Is that common in celiac disease? I have been putting the recommended eye drops but have not felt any significant improvement tbh.

It takes up to a year to heal from celiac disease as the learning curve for the gluten free diet is steep and other parts of the body, besides the small intestine, may be damaged.  Eye issues are common with autoimmune.  You might consider giving yourself more time to heal.  If not, see an ophthalmologist who knows about autoimmune issues.  

When I was diagnosed, I had a hard time seeing.  I almost did not pass the DMV eye test when I went for my driver’s license renewal and I was wearing brand new glasses!  Within a year or so, my eyes were better.  My prescription has continued to improve over the past six years. 

I do struggle with Ocular Rosacea, which is linked to my Hashimoto’s Thyroiditis and/or my autoimmune gastritis.  It ebbs and flows.  It can be made much worse with a gluten exposure.  

Since you have had your eyes examined a few times and doctors did not find anything specific, concentrate on healing from celiac disease.  It might be the root cause of your eye issues.  

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

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,112
    • Most Online (within 30 mins)
      7,748

    cam4180
    Newest Member
    cam4180
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • StaciField
      There’s a Cosco in Auckland in New Zealand. It’s a bit away from where I live but it’s worth the travel for me. Very appreciative of your advice.
    • Wheatwacked
      It seems you have proven that you cannot eat gluten.  You've done what your doctors have not been able to do in 40 years. That's your low vitamin D, a common symptom with Celiac Disease.  Zinc is also a common defiency.  Its an antiviral.  that's why zinc gluconate lozenges work against airborne viruses.  Vitamin D and the Immune System+ Toe cramps, I find 250 mg of Thiamine helps.   When I started GFD I counted 19 symptoms going back to childhood that improved with Gluten Free Diet and vitamin D. I still take 10,000 IU a day to maintain 80 ng/ml and get it tested 4 times a year. Highest was 93 ng/ml and that was at end of summer.  Any excess is stored in fat or excreted through bile.   The western diet is deficient in many nutrients including choline and iodine.  Thats why processed foods are fortified.  Celiac Disease causes malabsorption of vitamins and minerals from the small intestine damage.  GFD stops the damage, but you will still have symptoms of deficiency until you get your vitamins repleted to normal.  Try to reduce your omega 6:3 ratio.  The Standard American Diet is 14:1 or greater.  Healthy is 3:1.  Wheat flour is 22:1.  Potatoes are 3:1 while sweet potatoes are 14:1.  So those sweet potatos that everyone says is better than Russet: they are increasing your inflammation levels.   
    • Scott Adams
      My mother also has celiac disease, and one of her symptoms for many years before her diagnosis was TMJ. I believe it took her many years on a gluten-free diet before this issue went away.
    • Jeff Platt
      Ear pain and ringing your entire life may or may not be TMJ related but could be something else. A good TMJ exam would be helpful to rule that out as a potential cause from a dentist who treats that. I have teens as well as adults of all ages who suffer from TMJ issues so it’s not a certain age when it shows up.   
    • cristiana
      Not sure if related to coeliac disease but my ear ringing  has stepped up a notch since diagnosis.  Even since a child silence really hurts my ears - there is always a really loud noise if there is no other noise in a quiet room - but my brain has learned to filter it out.  Since diagnosis in my forties I also get a metallic ringing in my ears, sometimes just one, sometimes both.  But it comes and goes.   My sister also suffers now, we are both in our fifties, but she is not a coeliac, so for all I know it could just be an age thing.  I do get occasional stabbing pain in my ears but that has been all my life, and I do appear to be vulnerable to outer ear infections too.  So not a particularly helpful reply here, but I suppose what I am trying to say is it might be related but then again it could just be one of those things.   I think in the UK where I live doctors like you to report if you get tinnitus in just the one ear.  I reported mine but no cause was found.  Most of the time it is nothing but sometimes it can have a cause that can be treated, so perhaps worth reporting to your GP.  
×
×
  • Create New...