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

Orange Juice Sucks...

puggirl

Recommended Posts

puggirl Apprentice
puggirl
Posted

Well I used to be able to drink OJ but in recent years I just can't digest it. Its too acidic for me. My BF always Nags me you need more juice and fruit... Yeah yeah I know.. So today he was drinking Odwalla OJ and said here have some.. I cringed and said Ok ONE sip.. I took one sip and New it was a mistake. I was Feeling good ALL day no stomach problems, As soon as I drank that I felt like I was gonna throw up. I can feel it in my throat the OJ, I burshed my teeth to get the taste gone, chewed gum, had a mint, ate a couple of chips... But nooo.. It just feels like it burns my stomach. So Im never and I mean NEVER drinking OJ again, I don't care if its the only between me and Death! Does anyone else have issues with OJ? I cant even eat Oranges anymore, I used to love them.

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

Celiac.com Sponsor (A8-M):


weluvgators Explorer
weluvgators
Posted

Our super, super silly DD seemed to start reacting to "oranges" out of the blue when we went really gluten free initially for her. If we are very selective about which orange juice and oranges that we make available to her now, she seems to do well with them. I am not convinced that her issue was with "oranges".

On the other hand, I have had a lifetime issue with pulp in orange juice. You could not make me drink the stuff unless I strained it. Now, that was a result of visiting my grandparents in Florida when I was 5 years old and totally overdosing on orange juice. :o oops!

Liveenjoylife Apprentice
Liveenjoylife
Posted

I am going to go out on a limb here and ask. Do you have an intolerance to orang juice? Imo it sounds like just from that little sip, you may....I have the same prob with shrimp. I could eat it before, but just a little bite will send my stomach doing cart wheels. So horrible.

samcarter Contributor
samcarter
Posted

I haven't been able to eat oranges or drink orange juice for years now; it makes my psoriasis flare up horribly. I drink a glass, enjoy it, and within a day my psoriasis is bright red and painful, not just itchy.

GottaSki Mentor
GottaSki
Posted

I found out I couldn't tolerate OJ about a year ago...couldn't believe it because I love it...I've switched to AJ and some other mixed juices.

Has anyone been able to go back to OJ after healing with gluten-free?

Thanks!

puggirl Apprentice
puggirl
Posted
  • Author

Acouple of years ago I was able to drink OJ and eat oranges, but outta No where they started making me ill, So its interesting to hear other people have the same issues as I.

heatherjane Contributor
heatherjane
Posted

I used to eat oranges almost every day before going gluten-free. Now, about 30 mins after eating one I'll get a sharp pain in my gut. I laid off of them for a while because I thought it was a fluke, but once I started eating them again, the same situation happened. I'm wondering if it's just the acidity and now my body can't handle it anymore.

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

Celiac.com Sponsor (A8-M):


digmom1014 Enthusiast
digmom1014
Posted

I was just wondering the same thing. I had a few sips of OJ and felt naucious for the rest of the day. I'm not usually and OJ drinker-I drink V-8 so, I had never noticed.

Is this a celiac thing or an allergy/intolerance thing? Anyone?

mattathayde Apprentice
mattathayde
Posted

whats your blood type?

there is a book called "eat right for your type" and for those of us with O orange juice is bad. all the foods are put into 3 categories: good, neutral, and bad. ironically wheat is listed as bad for O's too.

it suggests that O types drink pineapple juice along with a few others but i dont remember which exactly off hand, but my dad has tried to stick to pineapple juice and has had less issues than when he drank OJ

-matt

CaraLouise Explorer
CaraLouise
Posted

I have had problems with all juices, but can eat the fruit fine. I think it has to do with a fiber issue.

mattathayde Apprentice
mattathayde
Posted
I have had problems with all juices, but can eat the fruit fine. I think it has to do with a fiber issue.

could also be the added sugar

-matt

samcarter Contributor
samcarter
Posted
whats your blood type?

there is a book called "eat right for your type" and for those of us with O orange juice is bad. all the foods are put into 3 categories: good, neutral, and bad. ironically wheat is listed as bad for O's too.

it suggests that O types drink pineapple juice along with a few others but i dont remember which exactly off hand, but my dad has tried to stick to pineapple juice and has had less issues than when he drank OJ

-matt

Eh. I have blood type B and while OJ was one of my favorite juices, I can't drink it anymore. I've read the blood type book and it claims type B can eat dairy...I can't eat dairy. I think a lot of that is coincidental. O is the most common blood type, and since celiac is estimated to be in 1 in 133 people...stands to reason most people with celiac would have type O blood.

Oranges don't hurt my stomach per se, but they make my immune system go haywire, triggering my psoriasis.

Pegleg84 Collaborator
Pegleg84
Posted

I've had trouble with orange juice too. If i just have a little it's okay, but too much makes me nauseous. Eating oranges is no problem though. It might very well be the acidity. I also seem to have trouble with tomatoes lately too. Do you have any problem with tomatoes or other relatively acidic foods?

Peggy

puggirl Apprentice
puggirl
Posted
  • Author

Yeah Tomatos Are Not good...

Pegleg84 Collaborator
Pegleg84
Posted

in that case, it's probably not the juice or fruit per se but the acidity level. It's funny cause I had tomato in my salad at noon today and felt a little funny after, and same with the guacamole i made tonight. figured it was just my cold.

anyone else got tomato problems?

  • 8 years later...
Jc59 Newbie
Jc59
Posted

Since I became gluten sensitive, I'm unable to drink OJ, and eat citric fruits either.  I looking for other foods for my vitamin C intake.  Are their any suggestions on other foods that will provide vitamin C?   

kareng Grand Master
kareng
Posted
45 minutes ago, Jc59 said:

Since I became gluten sensitive, I'm unable to drink OJ, and eat citric fruits either.  I looking for other foods for my vitamin C intake.  Are their any suggestions on other foods that will provide vitamin C?   

There is this interesting thing called " Google".  You can find things like this 

Open Original Shared Link

 

 

?

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      131,949
    • Most Online (within 30 mins)
      7,748
    Stephanie94
    Newest Member
    Stephanie94
    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

    • Jacki Espo
      Covid caused reoccurrence of DH without eating gluten

      By Jacki Espo · Posted

      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      New Celiac Mama in My 30s

      By Mari · Posted

      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      My only proof

      By Mari · Posted

      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
      Does anyone here also have Afib

      By knitty kitty · Posted

      Fascinating.
    • DebJ14
      Does anyone here also have Afib

      By DebJ14 · Posted

×
×
  • 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.