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

Goldfish Crackers, Cheesenip?


MaryanneQ

Recommended Posts

MaryanneQ Apprentice

Has anybody found a substitute for Goldfish crackers or Cheese Nips/Cheeze-Its? (Peppridge Farms I believe make them)

My son just loves these and obviously cannot have them any longer. Please let me know if there are any gluten-free alternitives out there :)

THANKS!

Maryanne


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



Celiac.com Sponsor (A8-M):



GFdoc Apprentice

I saw a recipe for gluten-free goldfish crackers using chebe bread mix. It was on their website www.chebe.com under recipes. I believe you add chedder cheese to the mix and roll it out thin, and cut it into fish shapes (if you have the patience)

I haven't tried it, but it sounds good.

Sara

Guest jhmom

Crunch Toons are the closest I have found to goldfish crackers and they are gluten-free. I found them at my local Target store. Open Original Shared Link is the website where you can check them out, they have original, cheddar cheese and nacho cheese flavor. I tried the cheddar cheese, they are shaped like tweety bird.

Boojca Apprentice

Jhmom, are you SURE these are gluten-free??? Sounds too good to be true, to this mom of a 2 1/2 year old who is NOT happy about giving up his goldfish. Please say it's so!!!!

Are they all gluten-free? (the flavors, I mean)

Bridget

Guest jhmom

Yes they are gluten-free, they are made from potato's!!!! Cool huh?

angel-jd1 Community Regular

They are VERY Yummy!! I LOVE the taz ones!!

-Jessica

Boojca Apprentice

I was just coming on to say I bought a bag, then read the ingredients and wondered if anyone had talked to the company? There's caramel coloring, and natural/artificial flavors. I wanted to be sure this is really ok before I give it to my two year old, who doesn't get diarrhea or anything like that for me to be able to know if he's had a 'mistake' His only symptoms, which lead to diagnosis, were that he was very lethargic and literally starving to death (he looked like an ethiopian, honest to god) and I really don't want to get to that point again before I realize something is wrong. I was going to contact the company tomorrow but if anyone has already done this, or has eaten these things long enough to know (aka their body would've told them) they are truly ok that's good enough for me.

Please lemme know! Thanks!!

Bridget


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



Celiac.com Sponsor (A8-M):



Guest jhmom

Hi Bridget

I am VERY sensitive too, even to the slightest crumb or cross contamination and did not have a reaction to them . I have not call the company to verify though.

I found out about Crunch Toons through another support group because the product was posted on the home page as a "safe snack" for Celiac's.

Maybe you should call the company just to make sure :D not unless someone else can verify this.

angel-jd1 Community Regular

Ok Silly Yaks, it is a sad day for me.....I have bad news to report :(

Crunch Toons the popular gluten-free snack made by Poore Brothers is being Discontinued. <_< I just got off the phone with the company and they are no longer making them!! You still might be able to find some on the shelves of stores such as Target, wal-mart etc. The lady on the phone said that they freeze well, so you can buy a bunch and put them into the freezer, but they are no longer being made!! I personally am SAD, because I LOVED the taz shaped ones. I know they were also great for little celiacs!! Just when we find something fun, it gets discontinued!! DARN!

Oh almost forgot, the whole reason I contacted them was to get firm confirmation of the gluten-free Status. They are gluten-free!! So If you find them, freeze them!! haha

-Jessica

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,130
    • Most Online (within 30 mins)
      7,748

    Tony White
    Newest Member
    Tony White
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • knitty kitty
      @rei.b,  I understand how frustrating starting a new way of eating can be.  I tried all sorts of gluten-free processed foods and just kept feeling worse.  My health didn't improve until I started the low histamine AIP diet.  It makes a big difference.   Gluten fits into opioid receptors in our bodies.  So, removing gluten can cause withdrawal symptoms and reveals the underlying discomfort.  SIBO can cause digestive symptoms.  SIBO can prevent vitamins from being absorbed by the intestines.  Thiamine insufficiency causes Gastrointestinal Beriberi (bloating, abdominal pain, nausea, diarrhea or constipation).  Thiamine is the B vitamin that runs out first because it can only be stored for two weeks.  We need more thiamine when we're sick or under emotional stress.  Gastric Beriberi is under recognised by doctors.  An Erythrocyte Transketolace Activity test is more accurate than a blood test for thiamine deficiency, but the best way to see if you're low in thiamine is to take it and look for health improvement.  Don't take Thiamine Mononitrate because the body can't utilize it well.  Try Benfotiamine.  Thiamine is water soluble, nontoxic and safe even at high doses.  I thought it was crazy, too, but simple vitamins and minerals are important.  The eight B vitamins work together, so a B Complex, Benfotiamine,  magnesium and Vitamin D really helped get my body to start healing, along with the AIP diet.  Once you heal, you add foods back in, so the AIP diet is worth doing for a few months. I do hope you'll consider the AIP diet and Benfotiamine.
    • captaincrab55
      Imemsm, Most of us have experienced discontinued, not currently available or products that suddenly become seasonal.   My biggest fear about relocating from Maryland to Florida 5 years ago, was being able to find gluten-free foods that fit my restricted diet.  I soon found out that the Win Dixie and Publix supper markets actually has 99% of their gluten-free foods tagged, next to the price.  The gluten-free tags opened up a  lot of foods that aren't actually marked gluten-free by the manufacture.  Now I only need to check for my other dietary restrictions.  Where my son lives in New Hartford, New York there's a Hannaford Supermarket that also has a gluten-free tag next to the price tag.  Hopefully you can locate a Supermarket within a reasonable travel distance that you can learn what foods to check out at a Supermarket close to you.  I have dermatitis herpetiformis too and I'm very sensitive to gluten and the three stores I named were very gluten-free friendly.  Good Luck 
    • rei.b
      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • knitty kitty
      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
    • rei.b
      I was tested for celiac at the same time, so I wasn't taking naltrexone yet. I say that, because I don't. The endoscopy showed some mild inflammation but was inconclusive as to celiac disease. They took several biopsies and that's all that was shown. I was not given a Marsh score.
×
×
  • 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.