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

Eye Issues


hannahp57

Recommended Posts

hannahp57 Contributor

I have been having some odd symptoms with my eyes in the past week or so. I have an appointment for wednesday of this week with the base opthamologist. I guess I just hoped maybe i could hear from someone before then that may be able to tell me if this has happened to others...

i got home from work on a monday night and had a pretty bad headache, i couldnt focus on anything and my eyes just felt so tired so i went to bed early. the next morning my eyes couldn't focus on anything and it was like they would barely stay open even though i wasnt sleepy because i had slept for over nine hours (which is a lot for me). i also noticed that every light in the house was hurting even worse, even my computer screen. and upon trying to put my contacts in my eyes burned very badly and the light sensitivity became worse. i havent been able to put them in since then. now i am noticing that i can read just as well with my glasses that are an old prescription from over four years ago. the light sensitivity will not go away. whenever i go outside i have to look at the ground. my pupils arent dilated and my head doesnt hurt at all. i just dont know what it could be. i have been on the gluten-free diet for three years this month so i dont think the diet could have caused this.

Any thoughts? I really just want to know if this is something i should be worried about? anyone ever go through vision problems like these?


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



Celiac.com Sponsor (A8-M):



daphniela Explorer

My eyes have been so bad that I was pretty much blind. Sitting in front of a computer for hours made it worse. It sounds like a migraine to me. I would start taking a magnesium pill daily and see if that helps.

hannahp57 Contributor

Everyone has told me you're having a migraine but i didnt think it was possible to have a migraine and not have a headache. the only migraine i ever had before was 7 years ago and i was SICK for hours. this isnt anything like that. could it still be a migraine? I will look into a magnesium supplement asap because i need to get my eyes back! i hope yours stop giving you problems too. if my opt tells me anything useful i'll post it on here. maybe we are having a similar issue?

daphniela Explorer

Migraines make you sensitive to light and sound. You don't nessesarily have to have a headache. Sometimes I have a headache with light sensitivity and sometimes I am just sensitive to the light. You will probably eventully get a headache. Migraines creep up on you and get worse, if you don't treat it right away.

daphniela Explorer

I forgot to add, excederin migraine is my best friend lol.

Mother of Jibril Enthusiast
I have been having some odd symptoms with my eyes in the past week or so. I have an appointment for wednesday of this week with the base opthamologist. I guess I just hoped maybe i could hear from someone before then that may be able to tell me if this has happened to others...

i got home from work on a monday night and had a pretty bad headache, i couldnt focus on anything and my eyes just felt so tired so i went to bed early. the next morning my eyes couldn't focus on anything and it was like they would barely stay open even though i wasnt sleepy because i had slept for over nine hours (which is a lot for me). i also noticed that every light in the house was hurting even worse, even my computer screen. and upon trying to put my contacts in my eyes burned very badly and the light sensitivity became worse. i havent been able to put them in since then. now i am noticing that i can read just as well with my glasses that are an old prescription from over four years ago. the light sensitivity will not go away. whenever i go outside i have to look at the ground. my pupils arent dilated and my head doesnt hurt at all. i just dont know what it could be. i have been on the gluten-free diet for three years this month so i dont think the diet could have caused this.

Any thoughts? I really just want to know if this is something i should be worried about? anyone ever go through vision problems like these?

I'm glad to hear that you're going to see an opthamologist... it could be something more serious like vasculitis. S/he should dilate your eyes and take a look at the blood vessels.

Is this something that just started? Have you had symptoms like this before?

hannahp57 Contributor

yeah it just started a week or so ago. but i didnt know if it was just something that irritated my eyes. but it wouldnt go away so i called as soon as the clinic opened this morning. toda has been cloudy and no lights in the house have been turned on so i feel perfectly fine today. im not putting contacts in again until i know whats going on. thanks for all the responses. i feel better hearing from others


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



Celiac.com Sponsor (A8-M):



dilettantesteph Collaborator

When I went gluten free one eye went from 20/40 to 20/20 and the other from 20/80 to 20/40. I felt like I could see better without my glasses than with them. Yet, my opthamologist said that my prescription hadn't changed. Weird right? I had blurred vision issues when eating gluten that went away.

hannahp57 Contributor

Just an update: Dr told me that it was probably bacteria in my contact that got in my eyes and were irritatig it. since it never became inflamed or puffy he said it probably hadnt actually become a full blown infection but would have had i continued wearing contacts. apparently bacteria in your eyes can make you very sensitive to lights... the problems have gotten better.

thanks for all the replies. it made me feel better just to hear from other people

Mother of Jibril Enthusiast

Glad to hear that it was something simple and treatable :)

DOCKLEARFAN Apprentice
Glad to hear that it was something simple and treatable :)

It seems that your issue is resolved, thats great !! On a similar note, there ARE lots of cases of "eye aches" with celiac people.

I'm doing some more research on that now...

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to Charlie1946's topic in Related Issues & Disorders
      40

      Severe severe mouth pain

    2. - knitty kitty replied to Charlie1946's topic in Related Issues & Disorders
      40

      Severe severe mouth pain

    3. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      1

      New issue

    4. - knitty kitty replied to GlutenFreeChef's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      Blood Test for Celiac wheat type matters?

    5. - trents replied to Charlie1946's topic in Related Issues & Disorders
      40

      Severe severe mouth pain

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,085
    • Most Online (within 30 mins)
      7,748

    kk007
    Newest Member
    kk007
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • cristiana
      I agree.  If someone has Barrett's Esophagus, at least here in the UK, as I understand it under normal circumstances a PPI needs to be taken long term (or similar medication).  I have two friends with this.  The PPI it does have side effects but they still have to take it.  
    • knitty kitty
      Do talk to your doctor about making changes to your medication.    I'm not a medical doctor.   I'm a microbiologist.  I studied nutrition before switching to microbiology because I was curious what vitamins were doing inside the body. I would hate to give advice that jeopardizes your health, so do discuss things with your doctor.   
    • knitty kitty
      @Jmartes71, Sorry you've been feeling so poorly.   Are you taking any medication to treat the SIBO?   Are you taking any Benfotiamine?  Benfotiamine will help get control of the SIBO.  Thiamine deficiency has symptoms in common with MS. Have you had your gas appliances checked for gas leaks and exhaust fume leaks?  Carbon Monoxide poisoning can cause the same symptoms as the flu and glutening.  Doctors have to check venous blood (not arterial) for carbon monoxide.  Are other inhabitants sick, or just you?  Do they leave the house and get fresh air which relieves their symptoms?  
    • knitty kitty
      European wheat is often a "soft wheat" variety which contains less gluten than "hard wheat" varieties found in the States.   In European countries, different cooking methods and longer  fermentation (rising or proofing) times allow for further breakdown of gluten peptides. Wheat in the States is a blend of hard and soft wheat.  Gluten content can vary according to where the wheat was grown, growing conditions, when harvested, and local preference, so a blend of both hard and soft wheat is used to make a uniform product.   I moved around quite a bit as a child in a military family.  I had different reactions to gluten in different areas of the country every time we moved.  I believe some wheat breeds and blends are able to provoke a worse immune response than others.   Since European soft wheat doesn't contain as much gluten as American wheat, you may try increasing your intake of your soft wheat products.  A minimum of ten grams of gluten is required to get a sufficient immunological response so that the anti-gluten antibodies leave the intestines and enter the bloodstream where they can be measured by the tTg IgA test.  Your whole wheat bread may only have a gram of gluten per slice, so be prepared...  
    • trents
      From my own experience and that of others who have tried to discontinue PPI use, I think your taper down plan is much too aggressive. It took me months of very incremental tapering to get to the point where I felt I was succeeding and even then I had to rely some days on TUMS to squelch flareups. After about a year I felt I had finally won the battle. Rebound is real. If I were you I would aim at cutting back in weekly increments for two weeks at a time rather than daily increments. So, for instance, if you have been taking 2x20mg per day, the first week cut that down to 2x20mg for six days and 1x20 mg for the other day. Do that for two weeks and then cut down to 2x20mg for five days and 1x20 for two days. On the third week, go 20x2 for four days and 20x1 for 3 days. Give yourself a week to adjust for the reduced dosage rather than reducing it more each week. I hope this makes sense. 
×
×
  • 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.