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

Microwave Popcorn

swittenauer

Recommended Posts

swittenauer Enthusiast
swittenauer
Posted

I really need some help this time. My husband would love nothing more than to have some popcorn tonight. I bought some Cousin Willie's Movie Theater Butter Microwave Popcorn. Anyone know if microwave popcorn is okay? The ingredients are as follows: Popcorn, partially hydrogenated soybean oil, salt, natural & aritifical flavors & beta carotene coloring. Thanks!

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

Celiac.com Sponsor (A8-M):


Rachel--24 Collaborator
Rachel--24
Posted

I've never heard of that brand of popcorn. Do you have the Delphi list? I found it to be very helpful. I printed the whole list and then stapled each section. I filed each section into one of those folding type file thingys. I labeled each section so its very convenient. If I want to look for popcorn I just pull out the "snack foods" and just pick something off the list. I checked the list for Cousin Willy's but its not on there so I don't know if its gluten-free or not.

swittenauer Enthusiast
swittenauer
Posted
  • Author

What about microwave popcorn in general?

Rachel--24 Collaborator
Rachel--24
Posted

Yes, there are brands that are gluten-free. Here are some:

Act II

Jolly Time

Orville Redenbacher All variteies gluten-free except the caramel pour-over popcorn & Ultimate Theatre Style w/ BBQ Flavour pouch

I'm sure there are more...I just got these from the list right now.

mytummyhurts Contributor
mytummyhurts
Posted

You know what is really good for popcorn and is not that hard to do?

There's a microwave popcorn popper by Presto. It is a plastic bowl with a conductive base. It was about $15 dollars and you have to buy these little paper things to go in the bottom to make the popcorn pop, but they are not expensive and you can re-use them so they last a long time. You use kernels of popcorn and put it in for 3 minutes and put your own butter and salt on it. It makes it so you can have as much butter that you want, but not too much. After I started using it I noticed that regular microwave popcorn feels like it has a film on it. And any ingredient that starts with "partially hydrogenated" is really bad for you.

tarnalberry Community Regular
tarnalberry
Posted

Nothing beats air-popped popcorn! :-) Poppers are around $15 at Target.

swittenauer Enthusiast
swittenauer
Posted
  • Author

We really like microwave popcorn. I would assume that since several of the major brands are gluten free that this brand is also but I guess I'll get some Act II & wait to hear from our brand.

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

Celiac.com Sponsor (A8-M):


Guest Lucy
Guest Lucy
Posted

I havn't seen a plain or just butter flavored popcorn that did contain gluten. I only do the microwave too. So easy and less clean up. I think it tastes BETTER than airpopped. Everyone has their own opinion.

mytummyhurts Contributor
mytummyhurts
Posted

Well, I prefer the taste of real butter to the powdery, slimy stuff.

elonwy Enthusiast
elonwy
Posted

I do it the super-old fashioned way ( I grew up with no electricity so have some weird habits).

I take a large pot and put in one-two tablespoons olive oil, which is heart healthy and gives the popcorn a wonderful nutty flavor, heat the oil, put popcorn in, then shake vigorously over flame until the popping stops. Then I put on butter and salt, sometimes shredded cheese or parmesan, and sometimes Furikake (there are two types that are gluten-free) and sometimes all of them!

Of course I consider popcorn a complete meal, so there you have it.

When I'm feeling lazy I just pop it in the microwave (always ORville) and then add stuff.

I used to put in little rice cakes (Arare), but they have soy sauce on them so I can't have them anymore. :(

Elonwy

Guest Lucy
Guest Lucy
Posted

Thats how we made it growing up too, I had forgotten that. Thanks for bringing back so fond memories. It must have been before I was 7 or 8 , so many years ago.....it was such a treat. Then we got an air popper, then the microwave came around. I feel old now.

  • 2 weeks later...
swittenauer Enthusiast
swittenauer
Posted
  • Author

Well, still no response from Cousing Willie's. I guess it is safe to assume that the answer would be that it is full of gluten. Who knows? Anyway, we are sticking with Act II. The Movie Style Butter popcorn is awesome & totally addictive.

skoki-mom Explorer
skoki-mom
Posted

I take Orville's micro popcorn to work on night shift. I eat a LOT of popcorn, even before my celiac disease dx, so was I ever glad my favourite snack was safe! I only make hot air popped at home, and put real butter on it, mmmmmmmmm. I have zero guilt about it because I just think of all the stuff I can't have!! I can't watch Survivor or a hockey game without my 'corn!

swittenauer Enthusiast
swittenauer
Posted
  • Author

I never ate a lot of popcorn before my husband was diagnosed & it became one of his favorite snacks. Now I find myself taking a bag of it for lunch. I'm hooked.

scottsuzann Newbie
scottsuzann
Posted
I've never heard of that brand of popcorn. Do you have the Delphi list? I found it to be very helpful. I printed the whole list and then stapled each section. I filed each section into one of those folding type file thingys. I labeled each section so its very convenient. If I want to look for popcorn I just pull out the "snack foods" and just pick something off the list. I checked the list for Cousin Willy's but its not on there so I don't know if its gluten-free or not.

<{POST_SNAPBACK}>

Ok... New here, what is the delphi list and how do i get one? :huh:

Thanks,

Suzann

grantschoep Contributor
grantschoep
Posted
Ok... New here, what is the delphi list and how do i get one? :huh:

Thanks,

Suzann

<{POST_SNAPBACK}>

People can probably mail it to you on here. But I figure its easy enough just to go straight to the source.

Open Original Shared Link

You'll need to register and make a log in. But then you can always grab it when needed and updated. Actually, I think you can just grab them as guest, don't know, already have all my login stuff. Just go to messages tab, and the first section of messages is gluten-free Product list.

Eliza13 Contributor
Eliza13
Posted

My favourite way to have popcorn is by using a pot, olive oil and kernels. Nothing beats it....it is delicious!! I salt them when they're done.

Guest arnelwendy
Guest arnelwendy
Posted
I've never heard of that brand of popcorn. Do you have the Delphi list? I found it to be very helpful. I printed the whole list and then stapled each section. I filed each section into one of those folding type file thingys. I labeled each section so its very convenient. If I want to look for popcorn I just pull out the "snack foods" and just pick something off the list. I checked the list for Cousin Willy's but its not on there so I don't know if its gluten-free or not.

<{POST_SNAPBACK}>

where do you get the delphi list

Archived

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

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


  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748
    LowellFrancis
    Newest Member
    LowellFrancis
    Joined
  • Celiac.com Sponsor (A20):

  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m
  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Rogol72
      Ibuprofen

      By Rogol72 · Posted

      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      Celiac and dermatitis herpetiformis has taken Me from Me

      By Jillian83 · Posted

      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
      Celiac and dermatitis herpetiformis has taken Me from Me

      By trents · Posted

      Is this man the father of your children?
    • Jillian83
      Celiac and dermatitis herpetiformis has taken Me from Me

      By Jillian83 · Posted

      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      Ibuprofen

      By cristiana · Posted

      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.