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Eye Floaters

JAS2

By JAS2
in Coping with Celiac Disease

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JAS2 Rookie
JAS2
Posted

Has anyone ever experienced eye floaters as a reaction to gluten?

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Celiac Mindwarp Community Regular
Celiac Mindwarp
Posted

There was a thread a while back on this, sorry I can't seem to link to it from my phone. Definitely people with advice.

Can be a warning for retinal detachment among other things.

Pegleg84 Collaborator
Pegleg84
Posted

I've got them. I don't think it has anything to do with Celiac in particular. "Floaters" are bits of detached tissue floating around in your eye. If they suddenly show up, or get worse, you should see a doctor/optometrist as soon as you can, since it could be a sign of something more serious like a detached retina.

I might notice them more when I've been glutened, but then again my vision is generally less focused when I've been glutened.

nvsmom Community Regular
nvsmom
Posted

It is also linked to uveitis (sp?) which can be potentially serious. Definitely a good idea to get it checked if you noticed a change.

cavernio Enthusiast
cavernio
Posted

My eye exam a couple weeks ago, my eyes has actually gotten better for the first time since I was a kid. That's not floaters though. I've had floaters for as long as I can remember, same place, same shape.

Opa3 Apprentice
Opa3
Posted

I've got them. I don't think it has anything to do with Celiac in particular.

My opthalmologist (of many years) never connected gluten to my floaters either.

Jen-1984 Apprentice
Jen-1984
Posted

I have a ton of eye floaters and issues with my eyes. I don't know what could cause it really but I have read other people on this forum say they have floaters and I have suspicions and it is my opinion that celiac maybe able to cause it. It is an autoimmune disease and effects every person differently. Gluten causes the autoimmune response. Now that I have been gluten and dairy free, I can count on one hand how many floaters I have had. Before I would see them several times a day. It is only my opinion and I am no doctor, but I feel there is a connection.

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Em314 Explorer
Em314
Posted

If followed by headache, they could also be migraine auras.

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      Celiac support is hard to find

      By tiffanygosci · Posted

      EDIT: I did find a monthly Zoom meeting for Celiacs through the Celiac Disease Foundation, so I'll be able to talk with some other people on January 15. And I also found a Celiac Living podcast on Spotify made by a celiac. I feel a little bit better now and I am still hoping I will find some more personal connections in my area.
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