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

How Would A Gluten Free Chex Mix Go Down With The Glutenoids


kellynolan82

Recommended Posts

kellynolan82 Explorer

Seeing as though Chex Cereals in the USA are gluten free (at least 5 of them are), I thought I'd order some varieties from USA foods and make up some chex mixes for a gathering I plan to have in a few weeks.

Do any of you have suggestions as to whether this would make a good munchy-snack type food? I've seen Cocoa Puffs, Kix and Trix cereals at my local IGA (they carry a number of international brands here at the one in the Canberra City) and they're ordering some Gluten Free Chex varieties in for me.

Do you think this would be palatable for others? I'm trying to think of foods that are great tasting despite all being gluten free. I don't want 'the "gluten free" thing' to come into it until I can help it. :rolleyes:


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



Celiac.com Sponsor (A8-M):



Darn210 Enthusiast

Absolutely!!! I use to make chex mix often . . . then they came out with it in the store. I always liked my home-made better but sometimes convenience won out. Now I'm back to making it only at home. I often have it at parties or take it to parties and I always get compliments on it because it's better than store bought. I always stick with the traditional but you can check out the chex web site for different varieties.

I only use the following ingredients:

corn chex

rice chex

mixed nuts

glutino pretzels

worcestershire sauce (Lea & Perrins (in the US))

butter

seasoned salt (Lawry's)

onion powder

garlic powder

kareng Grand Master

Here's an official recipe from the 60s. We never liked the Wheat Chex.

Chex.com has more variations

This is the authentic 1960s recipe:

3 tbsp cooking oil

1 tbsp peanut butter

Blend over low heat until blended ( I microwave)

Add: 1tbsp Worchestershire sauce

1/4 teasp garlic salt

1/4 tsp salt

In a 9x13 pan mix:

2 cups wheat Chex

2 cups corn Chex

2 cups rice Chex. ( I do 3 cups each corn & rice)

1/2 can salted peanuts

1 cup pretzels

Mix in the sauce. Bake at 200 F for 1 hour, stirring every 20 minutes.

You could use unsalted peanuts, low salt Worch. sauce & garlic powder to make it very low salt.

In the US Lea & Perrins is gluten-free.

Lisa Mentor

In the US Lea & Perrins is gluten-free.

Yes, Lea & Perrins is NOT gluten free in Canada. But some other brands are (can't remember what they are, though)

...yum, I love home make chex mix. :D

kellynolan82 Explorer

I'm in Australia and I found the Woolworths Select supermarket brand worchestershire to be the only one without gluten in it. Spring gully is another one that's apple cider vinegar based but I prefer Woolworths's one - less expensive for my liking.

Thanks for the tips everyone! Can't wait to get my hands on these delights. :D

StephanieL Enthusiast

I make a sweet snack we call "Monkey Much" for my kids. We have a long list of allergies as well as Celiac.

3/4 cup Sunflower seed butter

1 cup chocolate chips

Melt these two together in the microwave.

Add:

1 tsp. vanilla and stir

Add:

9 cups rice Chex

mix together (trying to be gentile)

Put 1 cup powdered sugar in a zip top bag. Add the cereal mixture. Add another cup of powdered sugar on top and shake to coat the cereal mixture.

(Commonly called Puppy Chow here too but with the changes I made, I felt I had the right to change the name ;) )

I *use* to use 1/4 cup coconut oil in the mix too which I really though added a little something to this but now DS is allergic to coconut so I just omitted it and it is still yummy. My family prefers this to the peanut butter kind too!

lovegrov Collaborator

I make gluten-free Chex mix every year at Christmas. I admit to missing the taste and texture contrast of t wheat Chex, but the mix is still tasty. And there are so many variations.

richard


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



Celiac.com Sponsor (A8-M):



mbrookes Community Regular

I entertain frequently and Chex mix is a favorite. No one has ever commented on the gluten-free part; they just wolf it down. Whenever I entertain I make all of the food gluten-free. If I can't eat it, I don't make it. Many party type foods are naturally gluten free. With the wide variety of gluten-free crackers now available making appetizers is a snap. This is one time I approve of "don't ask; don't tell".

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,948
    • 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):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • 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
    • DebJ14
×
×
  • 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.