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

Seeing Spots--Brief Flashes Of Light


collins146

Recommended Posts

collins146 Apprentice

does anyone on here see spots for just an instant? I've heard this can be due to malnutrition--possibly poor nutrient absorbtion. I've experienced this for a while and it seems to come and go. It went away when I was on st johns wort and also seemed to go away when I first went gluten free. Maybe serotonin?


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



Celiac.com Sponsor (A8-M):



DownWithGluten Explorer

does anyone on here see spots for just an instant? I've heard this can be due to malnutrition--possibly poor nutrient absorbtion. I've experienced this for a while and it seems to come and go. It went away when I was on st johns wort and also seemed to go away when I first went gluten free. Maybe serotonin?

Uh, maybe. I mean I don't know exactly what you're seeing. But definitely those times right before I've passed out...things get blotchy and spotty then all turns black :lol:

But there've been a few times in my life, if I'm lying down and get up suddenly or...something. I might see some splotches. A few times I've seen little sparking things. not really a light but...dunno what that is...look like little dull shooting stars or something that are there if I close my eyes too, lasting only a few seconds. And that's been only a few times in my entire life, and again I think it might have to do with blood flow to my head or something. Not sure if it's a gluten thing.

But I don't want to minimize what you're seeing because yours could be something different. Do you feel light-headed at the same time? That could be lack of food/blood flow thing going on. But I'd say if it happens often and intrusively you might want to get it checked out.

kbtoyssni Contributor

Seeing flashes of light and stars can mean a torn retina which is something you should see an eye doc about ASAP.

Black specs in your vision is usually usually caused by "floaters", small pieces of things like blood in the eyes. That's normal and nearly everyone has some.

opus88 Newbie

I have a huge issue with floaters - my eye doctor often comments that I have more than my share of them! Many times, as the tiny glob of vitreous fluid detaches, it can cause that little flash of light. It definitely warrants an eye exam just to be sure, but it likely is nothing more serious than that. If that is what's going on with you, other than it being annoying when floaters make it a little harder to see clearly, there is no real harm from it.

luvs2eat Collaborator

I've had several episodes in my life of flashing lights... sort of in a circle. The first time I had it I was in a grocery store and I kept blinking my eyes to see if it would go away. I wondered if it might be an "aura" and I was going to have a seizure or something!! About 20 min. later, the circle of flashing had reduced to maybe 1/4 of a circle. I ended up going to my ophthalmologist, who asked me if I'd experienced a wicked headache afterward? I hadn't. He told me it was an ophthalmic migraine... w/ no headache. I've had it maybe twice since that first time... in about 15 years.

RiceGuy Collaborator

I have had some brief slashes on rare occasions. More when I was little than later. Maybe just one "spark", and I could tell it wasn't actually emitting from any objects around me. There was one or two times when multiple flashes occurred within a second or two. Seems to me I read something about it someplace over the last year or two, but don't recall the details. Just that it happens to many people with Celiac. I'd guess malnutrition could possibly cause it.

irish daveyboy Community Regular

I have had some brief slashes on rare occasions. More when I was little than later. Maybe just one "spark", and I could tell it wasn't actually emitting from any objects around me. There was one or two times when multiple flashes occurred within a second or two. Seems to me I read something about it someplace over the last year or two, but don't recall the details. Just that it happens to many people with Celiac. I'd guess malnutrition could possibly cause it.

I've experienced flashes or darting light in conjunction with Migraine.

I know when an attack is coming on because I see zig-zag lines around the periphery of my vision.

As it progresses the zig zag line close into the centre of my vision. When I was young I was told that it was a sign of an upset stomach ??

As the Migraine progresses, bolts of pain can be felt along the eyebrows like someone shoving a 6" nail into your skull.

The pain then travels over the top of my head and manifests itself in the 2 tendons at the base of the skull.

After which I see darts of light, shooting stars.

I've read it's your brain visualizing neurons travelling along nerves towards your brain.

Anyway as soon as I notice the zig zag lines, I take a soluble pain killer (acts faster) and all is well.

I had these pre-Celiac and occasionally since, I believe they are 'stress' related.

Best Regards,

David


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

does anyone on here see spots for just an instant? I've heard this can be due to malnutrition--possibly poor nutrient absorbtion. I've experienced this for a while and it seems to come and go. It went away when I was on st johns wort and also seemed to go away when I first went gluten free. Maybe serotonin?

It could be lots of things but: When I was extremely anemic from this Celiacs, This sort of thing would happen more often. That was because my blood couldn't carry oxygen like it should. My Hub has this when he gets dehydrated.

Rondar2001 Apprentice

I have this occassionaly lasting up to 2 hours. After a clean MRI, my doctor said it is probably a migrane, I just don't get the pain that most people do. Still I would check it out just in case.

bluebonnet Explorer

i sometimes have these really quick specs or dots of a bright spot that go as fast as it came. i have several floaters. i also have had those ocular migranes where my eyes get really freaky vision and blackness going on. i have the "sparkly vision" sometimes too when i look at a bright sky or a white piece of paper... almost like fizzling fireworks. i go to the eye doc yearly to be safe. i always thought it to be from my insomnia, stress or now i'm paying for years of being a kid outside not wearing sunglasses.

bottom line, go to the eye doc to be sure it isn't anything harmful to your vision. B)

4berrys Newbie

Yes! This happens really badly when I have been getting trace gluten that creeps up on me! This last summer the floaters were so bad I had trouble concentrating on what I was reading :unsure: When I figured out what the mystery gluten was coming from and removed it, the floaters took months to go away still. I used to also get the 'lighted' floaters that looked like they were glowing from the corner of my eyes. My 17yo daughter also has visual disturbances when she gets gluten----floaters, flashes and dark 'clouds' out of the corners of her eyes. I just figure that since gluten causes neurological problems in us----this is just part of the toxic neurological response.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,561
    • Most Online (within 30 mins)
      7,748

    Valentino
    Newest Member
    Valentino
    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

    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
    • knitty kitty
      Hi, @Ginger38, I've had shingles in the past.  I understand how miserable you're feeling.   Not only do i have the chickenpox virus lurking about, I also have the cold sore virus that occasionally flares with a huge cold sore on my lip when stressed or exposed to gluten.  The virus lives dormant in the nerves on the left side of my face.  It causes Bell's Palsy (resulting in drooling).  The cold sore virus is also in my eye.  My eye swells up and my vision is diminished permanently whenever I have a flare, so it's of the utmost importance to keep flares away and treat them immediately if they do happen so I don't lose any more vision.   I take the amino acid supplement L-Lysine.  Lysine messes with the replication of viruses, which helps the body fight them off.   I haven't had an outbreak for several years until this year when exceptionally stressed and contaminated, it flared up again. Lysine has been shown to be beneficial in suppression of viruses like the cold sore virus (a herpetic virus), the chickenpox virus (also a herpetic virus), as well as the HIV virus, and even the Covid virus.   I also take additional Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) because Thiamine has antiviral properties as well.   For pain, a combination of Thiamine (like TTFD or Benfotiamine or Thiamine Hydrochloride), with B12 Cobalamine, and Pyridoxine B6 have been shown to have analgesic properties which relieve pain and neuropathy.    The combination of Thiamine B1, Pyridoxine B6 and Cobalamine B12 really does work to relieve pain.  I take it for back pain from crushed vertebrae in my back.  This combination also works on other pain and neuropathy.   I usually buy a supplement that combines all three and also Riboflavin B2 called EXPLUS online.  However, it's made in Japan and the price with the tariffs added makes it really expensive now.  But the combination of Thiamine B1, Pyridoxine B6 and B12 Cobalamine (and Riboflavin B2) still work even if taken separately.   I can't take Tylenol or ibuprofen because of stomach upsets.  But I can take the vitamin combination without side effects.  However, you can take the three vitamins at the same time as other pain relievers for added benefit.  The vitamins help other pain relievers work better. I hope you will try it.  Hopeful you'll feel better quickly. Interesting Reading: Thiamine, cobalamin, locally injected alone or combination for herpetic itching: a single-center randomized controlled trial https://pubmed.ncbi.nlm.nih.gov/23887347/ Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Analgesic and analgesia-potentiating action of B vitamins https://pubmed.ncbi.nlm.nih.gov/12799982/ A Narrative Review of Alternative Symptomatic Treatments for Herpes Simplex Virus https://pmc.ncbi.nlm.nih.gov/articles/PMC10301284/
    • Mari
      I think, after reading this, that you areso traumatized by not being able yo understand what your medical advisors have been  what medical conditions are that you would like to find a group of people who also feel traumatized who would agree with you and also support you. You are on a crusade much as the way the US Cabinet  official, the Health Director of our nation is in trying to change what he considers outdated and incorrect health advisories. He does not have the education, background or experience to be in the position he occupies and is not making beneficial decisions. That man suffered a terrible trauma early in his life when his father was assonated. We see now how he developed and worked himself into a powerful position.  Unless you are willing to take some advice or  are willing to use a few of the known methods of starting on a path to better health then not many of us on this Celiac Forum will be able to join you in a continuing series of complaints about medical advisors.    I am almost 90 years old. I am strictly gluten free. I use 2 herbs to help me stay as clear minded as possible. You are not wrong in complaining about medical practitioners. You might be more effective with a clearer mind, less anger and a more comfortable life if you would just try some of the suggestions offered by our fellow celiac volunteers.  
    • Jmartes71
      Thus has got to STOP , medical bit believing us! I literally went through 31 years thinking it was just a food allergy as its downplayed by medical if THEY weren't the ones who diagnosed us! Im positive for HLA-DQ2 which is first celiac patient per Iran and Turkey. Here in the States especially in Cali its why do you feel that way? Why do you think your celiac? Your not eating gluten so its something else.Medical caused me depression. I thought I was safe with my former pcp for 25 years considering i thought everything I went through and going through will be available when I get fired again for health. Health not write-ups my health always come back when you're better.Im not and being tossed away at no fault to my own other than shitty genes.I was denied disability because person said he didn't know how to classify me! I said Im celiac, i have ibs, hernia, sciatica, high blood pressure, in constant pain have skin and eye issues and menopause intensified everything. With that my celiac nightmare began to reprove my disregarded disease to a bunch of clowns who think they are my careteam when they said I didn't have...I feel Im still breathing so I can fight this so no body else has to deal with this nightmare. Starting over with " new care team" and waisting more time on why I think I am when diagnosed in 1994 before food eliminated from my diet. P.s everything i went through I did write to medical board, so pretty sure I will continue to have a hard time.
×
×
  • 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.