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

Anyone Else Have Trouble With gluten-free Breads?


ebrbetty

Recommended Posts

Guest southgoingzax

I was terrified too, of getting a colonoscopy. I told my doctor to mske sure I was completely out, not just mildly sedated. As soon as I woke up I got the heck out of there! Now that it's over, it doesn't seem that dramatic, but beforehand I thought I was going to die from nerves and well, yes, embarrassment. So, you'll survive - it wont be that bad.

In regards to the bread - everyone here has a good point - it could be any one of the ingredients causing the issue. I am sensitive to fructose, so too much of that in a bread can give me DH, and I'm allergic to dairy and eggs and soy, so I have to find breads without those ingredients. I know there are some mixes out there made of fava, garbanzo bean, and/or mesquite flour - you may have to do some searching, but those might be alternatives.

zax


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



Celiac.com Sponsor (A8-M):



whitball Explorer

I have had problems with brown rice breads, with fruit juice. I can't remember the name of it. I ate some yesterday and it burned my throat. Kind of a wierd experience.

Mia H Explorer
My fave so far is the 4-flour bread in Bette Hagman's The Gluten Free Gourmet Bakes Bread, using the sesame variation & replacing all sugar with molasses. It isn't all sorghum, just one of the ingredients, but it seems to make a big difference.

Leah

I looked at this recipe and it has tapioca flour in it. In fact ALL of Bette's recipes for bread do that I have ever seen. Does anyone know of a good replacement for tapioca?

Mia

queenofhearts Explorer
I looked at this recipe and it has tapioca flour in it. In fact ALL of Bette's recipes for bread do that I have ever seen. Does anyone know of a good replacement for tapioca?

Mia

Sorry, I'd forgotten that this thread was supposed to be tapioca-free too. I'm not sure about the tapioca substitute, but I did find this sorghum bread with no tapioca. Haven't tried it myself but you might want to give it a go. Meanwhile I'll do some research on the tapioca.

Open Original Shared Link

Leah

penguin Community Regular

I use cornstarch to replace the tapioca starch in flour blends, and so far it works just fine :)

Annalise Roberts reccommended to use arrowroot starch in place of tapioca.

queenofhearts Explorer
I use cornstarch to replace the tapioca starch in flour blends, and so far it works just fine :)

Annalise Roberts reccommended to use arrowroot starch in place of tapioca.

I knew I remembered seeing a substitute somewhere, but couldn't remember what it was! Thanks, Chelsea!

Leah

skbird Contributor

That's funny, I was just mixing up the four flour blend yesterday - using arrowroot instead of cornstarch. So if I was sensitive to tapioca, then I'd be using a lot of arrowroot! I thought the arrowroot was interesting, has a scent to it which I've never noticed before as I've only used small amounts of it in recipes. I'm looking forward to making bread with this mix - I haven't had a good gluten free bread since Manna from Anna which I had to stop eating because of the corn (yeah, there are corn-free versions, too, but they have potato, which I can't have).

The only time I miss bread is also the hamburger/hot dog thing. My favorite bread product is Whole Foods pizza crusts - I don't think they have tapioca in them, but I could be wrong. Hard to believe I found something with no corn or potato! Mmmmmm....

Stephanie


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



Celiac.com Sponsor (A8-M):



Mia H Explorer

Thanks for the suggestion.

I was so bummed, I was really excited to make Bette's egg noodles for some comfort food-chicken noodle soup, and bought ALL the flours ($23 worth), then found out I could eat the tapioca :(

Mia

cjjolly Newbie

Hi:

I've been wanting to post my experiences here with Whole Foods Bread and Pizza Crust products. They taste fantastic, but every time I ate them I got D immediately after--not a major gluten reaction but very annoying nonetheless.

I wrote to Whole Foods and told them how disappointed I was with their product--that they must have some gluten in these products somewhere because I am not sensitive to anything on the label. They sent me a very thoughtful reply and I think the information is something everyone here should know. Apparently the US standard for "gluten-free" is 5 parts per million gluten and that the Whole Foods products adhere to this standard. In Canada it is zero parts per million. They suggested to me that I am perhaps very sensitive to gluten, thus reacting to the "5 parts per million". They also tried to suggest that it is something else within the bread. I don't think so because I make my own bread using most of the ingredients listed and have never had a reaction to the home-baked bread.

Guest Robbin

Thanks for that info cjjolly. I suspect that is the case with me as well. Some products immediately give me a reaction and other products with the same ingredients, no problems. Maybe it is the difference in

government allowances. I wish it were internationally standardized.

daffadilly Apprentice

yes, I cannot eat any of that stuff. It gives me a stomach ache & from there the symptoms are varied and last from a day or two to a week. So it was not hard to not eat them. I think all those grains are cross contaminated.

If I really want something like a banana bread I make it using almond flour.

Mia H Explorer
yes, I cannot eat any of that stuff. It gives me a stomach ache & from there the symptoms are varied and last from a day or two to a week. So it was not hard to not eat them. I think all those grains are cross contaminated.

If I really want something like a banana bread I make it using almond flour.

That sounds yummy, do you have a recipe?

Mia

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,955
    • Most Online (within 30 mins)
      7,748

    Mabelie
    Newest Member
    Mabelie
    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.