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

Sugar Causing Symptoms?


spirit-walk

Recommended Posts

spirit-walk Contributor

Do many of you have problems if you eat foods high in sugar even if they are natural sugars coming from fruit? Sugar triggers joint pain for me. Just wondering if there are others who experience symptoms from eating a lot of sugary fruit and such?


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



Celiac.com Sponsor (A8-M):



treesahope Newbie

Some say sugar is poison.  I say eat it rarely, and sparingly, but that is difficult to do after being celiac, you are limited already, it is too sad to "give up" sugar too.  Sugar is inflammatory so yes, joints may have an issue if you are that sensitive.  Sugar may be something you want to have rarely or barely.   I try so hard to not eat much, it is in many things, but I have backed off so much that I don't add as much to my coffee as I used to and I don't need as much as I used to.  Try carmalized onions and roasted carrots for your sweet treats and feel better.  Good luck.

Celiacandme Apprentice

I'm having a hard time with sugar. I'm also craving it! Not a good combo! How bad is your reaction?

FruitEnthusiast Enthusiast

Sugar is inflammatory so yes, joints may have an issue if you are that sensitive.  Sugar may be something you want to have rarely or barely.

 

I agree. I have had to cut way back on sugar too. I'm trying give it up completely. For now I'm trying to see how I do with just tiny amounts. It is hard to give up. Honey is supposed to be the best sweetener for you, but I've never cared much for it myself. I try to think of fruit as my dessert.

1desperateladysaved Proficient

Have you been tested for fructose intolerance?  I try to avoid sugar to stabilize my blood sugar.  For this reason I usually use bites of fruits rather than whole fruits and have them with meals.  A GI doctor told me last week that they tell people with fructose intolerance to eat it using this bite method..

Seeking2012 Contributor

Here's what eating white sugar, brown sugar, potatoes, rice, etc does to me:

 

• Depression

• Anxiety
• Brain Fog
• Inabilty to concentrate or think straight
• Fatigue
• Hypoglycemia symptoms
• Irritability, poor mood, crashing
• Bloating, water retention, and increased flatulence

 

I don't know why or how that happens because I was tested for pre-diabetes and diabetes and I'm negative on both. I have hyperinsulinemia though (chronic high insulin blood levels) so maybe it has to do with that. Perhaps sugar and starch is impacting my brain severely. I always feel better going low-carb. Maybe someone here knows more about how sugar impacts these things. have you tried a low-carb diet? I bake with almond flour exclusively now and use sugar substitutes.

FruitEnthusiast Enthusiast
Perhaps sugar and starch is impacting my brain severely. I always feel better going low-carb.

 

If you have gut inflammation or leaky gut, sugars, starches, or carbs can cause symptoms. The gut and brain are very closely connected. That's why we get brain fog from something our gut doesn't like. Are you familiar with the SCD diet? There's a lot of information on their site about this stuff and food recommendations. Even if you're not on the diet, it's helpful reading. You may know about it already but if not here's a link:

 

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



Seeking2012 Contributor

If you have gut inflammation or leaky gut, sugars, starches, or carbs can cause symptoms. The gut and brain are very closely connected. That's why we get brain fog from something our gut doesn't like. Are you familiar with the SCD diet? There's a lot of information on their site about this stuff and food recommendations. Even if you're not on the diet, it's helpful reading. You may know about it already but if not here's a link:

 

Open Original Shared Link

 

I'm assuming that if one has Celiac, then by definition they are dealing with intestinal permeability unless they got their number down to zero. But why would carbs cause problems for my brain when fat and/or protein would not? What's the reasoning or cause behind that? I have read about the specific carbohydrate diet before but I'm rusty so I'll read up on it.

FruitEnthusiast Enthusiast

I don't know if everyone with Celiac has intestinal permeability, it's not the same thing as flattened villi.

 

Starches (carbs) and sugar are similar. They cause inflammation and are what the bad gut bacteria feed on. Removing them helps restore the balance of good bacteria in the gut and reduces inflammation and that helps intestinal permeability heal.

 

Read more on the SCD site if you're interested, it's filled with all this information and more.

 

Good Luck!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,964
    • Most Online (within 30 mins)
      7,748

    Cbear
    Newest Member
    Cbear
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      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
      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
      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
×
×
  • 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.