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 Infections


LiveLoveLaugh04

Recommended Posts

LiveLoveLaugh04 Newbie

Hi all,

I need your advice regarding my problems with the left eye. I was diagnosed last May after being hospitalized (extreme dehydration caused by vomiting). So, they had to admit me since they were worried about my kidneys and had no idea what caused vomiting in the first place. I guess this was a blessing in disguise because for three years prior to this, I had various stomach problems but those doctors kept saying it could be stress (although I had no reasons to be stressed out). I am very strict about my diet. Unless it is written that is gluten-free, I do not eat it. Since October, I have been getting eye infections a lot. My eye looks bloodshot, sometimes itchy (not always), sometimes has a little yellow discharge, and tearing a lot. I also noticed that I do not see as well, esp. at night. Drs. gave me different eye drops, eventually it got better and than soon after, it would start all over again. My eye doctor even asked me: "are you sure there is a problem?" I am beyond frustrated and to be completely honest, extremely scared. I came across Sjorgen's syndrome and I am wondering if this could be it. Has anyone experienced this? If it is Sjorgen's, what is the best treatment for it?How dangerous is it? I am terrified of being diagnosed with something else. Next month I have to go for my check up with my gastroenterologist and I want to make sure to ask all the right questions.If you have any knowledge on this topic, please let me know. I would greatly appreciate your help. Thank you!


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



Celiac.com Sponsor (A8-M):



LauraTX Rising Star

It is plausible that something like Sjogrens could give you dry eye and make it more susceptible to infection.  Definitely follow up on that, and are you seeing an ophthalmologist?  If not, definitely make an appointment to get the eye looked at in depth, and discuss the possibility of that issue there.

Gemini Experienced

I have Sjogren's Syndrome and have had it for years before I was diagnosed.  Like you, I stumbled onto it after doing some research.  There is antibody blood testing that can be done but because it is an autoimmune issue, there are false negatives that can occur.  I would suggest a trip to an ophthalmologist and ask for testing. 

 

I did have some eye infections exactly as you described but only a couple of times.  My eyes were mainly blood red, dry and extremely uncomfortable and light sensitive.

I still have light sensitivity but use Restasis eye drops (Rx) every day and it has helped quite a bit.  Without them, my eyes are a mess.  I would say the only danger in having Sjogren's is not being diagnosed because having very dry eyes all the time can affect your vision.  I am not implying that you will go blind but your vision can become worse, you may need stronger glasses and you'll keep getting infections if the problems aren't addressed.  Restasis does not help everyone but you do not know unless you try it. 

 

Do you have dry mouth also and dental problems?  These are the hallmarks of Sjogren's as it just doesn't affect your eyes.  Try not to be scared and worry needlessly and yes.....I know that is not easy to do.  I have 4 AI diseases and am older so take everything in stride these days.  Things are gonna happen as you get older so the best thing to do is find out what the problems are and address symptoms to make your life more pleasant.  It would be far better to know that you may have Sjogren's than to keep going to all these doctors who just keep giving you eye drops for infections and not finding out why it is happening.

 

Good luck and keep us updated!  If you have any more questions, feel free to ask away!   :)

Renaye Contributor

I had many infections and trips to the dentist that indicated sjogren's but my blood work is negative but I am treated with plaquenil for fatigue and mild joint pain by my rheumatologist. I use systane eye drops and there is a night time gel by refresh that is really good. If your blood work is negative then they call it "sicca syndrome." Sjogren's can go hand in hand with celiac. My eyes got better after my stress level went down, plaquenil, eye drops and I quit wearing contacts and eye make-up. Hope

this helps.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,202
    • Most Online (within 30 mins)
      7,748

    PatBurnham
    Newest Member
    PatBurnham
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      NCGS does not cause damage to the small bowel villi so, if indeed you were not skimping on gluten when you had the antibody blood testing done, it is likely you have celiac disease.
    • Scott Adams
      I will assume you did the gluten challenge properly and were eating a lot of gluten daily for 6-8 weeks before your test, but if not, that could be the issue. You can still have celiac disease with negative blood test results, although it's not as common:  Clinical and genetic profile of patients with seronegative coeliac disease: the natural history and response to gluten-free diet: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606118/  Seronegative Celiac Disease - A Challenging Case: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9441776/  Enteropathies with villous atrophy but negative coeliac serology in adults: current issues: https://pubmed.ncbi.nlm.nih.gov/34764141/  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS.
    • Xravith
      I'm very confused... My blood test came out negative, I checked all antibodies. I suppose my Total IgA levels are normal (132 mg/dl), so the test should be reliable. Still, I'm not relieved as I can't tolerate even a single biscuit. I need to talk to my doctor about whether a duodenal biopsy is necessary. But it is really possible to have intestinal damage despite having a seronegative results? I have really strong symptoms, and I don't want to keep skipping university lectures or being bedridden at home.
    • Scott Adams
      They may want to also eliminate other possible causes for your symptoms/issues and are doing additional tests.  Here is info about blood tests for celiac disease--if positive an endoscopy where biopsies of your intestinal villi are taken to confirm is the typical follow up.    
    • Scott Adams
      In the Europe the new protocol for making a celiac disease diagnosis in children is if their tTg-IgA (tissue transglutaminase IgA) levels are 10 times or above the positive level for celiac disease--and you are above that level. According to the latest research, if the blood test results are at certain high levels that range between 5-10 times the reference range for a positive celiac disease diagnosis, it may not be necessary to confirm the results using an endoscopy/biopsy: Blood Test Alone Can Diagnose Celiac Disease in Most Children and Adults TGA-IgA at or Above Five Times Normal Limit in Kids Indicates Celiac Disease in Nearly All Cases No More Biopsies to Diagnose Celiac Disease in Children! May I ask why you've had so many past tTg-IgA tests done, and many of them seem to have been done 3 times during short time intervals?    
×
×
  • 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.