Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Green Giant Sweet Potato Chips


Adalaide

Recommended Posts

Adalaide Mentor

So I have almost bought these chips a few times in the store but they aren't labeled gluten free so I never did. Every time I was in the store and saw them it was in the evening and far too late to call customer service. Finally today my husband texted me and asked if I could have them. Their website didn't say anything about them being gluten free but they have no yeast or soy so I called. Apparently they are not considered gluten free because either of the manufacturing process or because the company could not source an ingredient, the rep couldn't say which because she didn't have access to that sort of information. 

 

In the end though, this is the same company that makes Trix. Trix are "not considered gluten free" but don't carry the same "may contain traces of" warning may GM cereals do. I eat it with no ill effects, it has no gluten containing ingredients. It falls under the same category by the company as the chips do. 

 

Has anyone else tried these chips? I'm not generally reckless, and I understand it is risky, but so are my bedtime Trix. (Which have never caused me harm, nor have Kix.) I'm quite tempted, but am curious to know if anyone else has tried them and been bitten or been fine. Or if I would be our first guinea pig. 


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Sounds like the company doesn't want to say gluten-free because it doesn't test for it. Many companies are doing that these days.

Adalaide Mentor

It is that she couldn't confirm if it was a manufacturing or sourcing thing that is nagging at me. Stupid hangups. I'm sure I'll eventually just eat a bag and see what happens. I mean, I eat Trix. They did tell me that everything from their company that they will say is gluten free is labeled gluten free. Exasperating. A year ago I was SO PARANOID about everything, and now I am mostly whole foods or at least real foods but I can't live in a freakin' bubble or in fear my whole life of everything that crosses my path.

Takala Enthusiast

Is this where I am supposed to suggest baked sweet potato homefries for supper ?  I don't want contribute to a possible migraine !  I ate through several bags of corn chips last Nov/Dec after years of abstaining, and thought I had a keeper, until the rash showed up.  And it became inflamed right along a critical underwear line.  And it was so bad I almost went to the doctor until I remembered that tea tree oil kills everything.   :ph34r:  :blink:  :lol:  But I had to stop eating the chips.  And they were so good.  I think I might try to grow popcorn this year. 

Adalaide Mentor

Nah, my migraines are only from tyramine! Sweet potato fries aren't the same as chips. I mean, I could make them but I have never managed crispy ones. I just want potato chips made out of sweet potatoes, it sounds like such a brilliant idea. :( Mostly I was hoping someone had previously tried them.

Takala Enthusiast

Isn't there some sort of nifty little chip holder cook thing that one puts in the microwave, and ends up with chips ?  You should search "microwave potato chip maker"  then see if you already have something you could fake this with, I think you just slice the potato thinly and lay it out on a friendly, non stick surface and zap it a lot. 

kareng Grand Master

These are yummy

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



psawyer Proficient

I understand that companies who don't test won't make a gluten-free claim. I understand why they don't test--the market is competitive, and the cost of the testing would increase the price for everybody, not just the 1 per cent or so who actually care.

So I eat products from a number of companies, including General Mills, but also Kraft, Unilever, ConAgra and Nestle (among others), who have a policy that they will clearly disclose on the label any known gluten content.

The world is a shared facility. I have no way of knowing if the mushroom I am buying in the produce department was touched by another customer who just ate from the salad bar and had a piece of bread.

There is always a risk of contamination, however small. I got used to it long ago.

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. - Katya773 posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Wholefoods 365 Organic Wheatgrass Powder

    2. - emily 1 replied to emily 1's topic in Coping with Celiac Disease
      8

      Black Pepper Reactions

    3. - Blue Roan replied to emily 1's topic in Coping with Celiac Disease
      8

      Black Pepper Reactions

    4. - Blue Roan posted a topic in Related Issues & Disorders
      0

      Irregular periods AFTER going gluten-free?

    5. - John Scott commented on dixonpete's blog entry in Pete Dixon
      9

      A video with researcher William Parker about Helminthic Therapy


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,009
    • Most Online (within 30 mins)
      7,748

    Jen44
    Newest Member
    Jen44
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      69.8k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Katya773
      Hi Everyone,   I recently purchased this wheatgrass not realizing that it wasn’t gluten free. I had two servings before I got really sick. Abdominal cramps , diarrhea and horrible nausea. My daughter read the label and told me it wasn’t labeled gluten free. I thought this was safe because supposedly it’s healthy. I called WholeFoods and they told me that they can find out more about the product and email me when it was picked and harvested. I was diagnosed back in 2019 and I really should know better! Anyone else had a reaction to wheatgrass powder? 
    • emily 1
      Yes, unfortunately I was diagnosed about 15 years ago. Some of us I guess the gut never heals and from what I've learned you can actually have a setback which is probably the stage I am at where I actually have become more sensitive to more items.
    • Blue Roan
      Hi Emily! I was just diagnosed a year ago and could not touch nuts, corn (or anything with corn-based ingredients), lactose, or black pepper in the first 8 or so months. Otherwise I had a lot of abdominal discomfort, dizziness/vertigo (especially with corn and pepper) and inflammation throughout the body. I was pretty much eating plain cooked veggies and chicken for the first few months because they were safe and reliable.  Over time, I have slowly started to tolerate some of the no-no foods, but my system is still sensitive to the pepper and has a limit to corn/lactose before symptoms occur. When you’re first diagnosed, you will likely be sensitive to a lot of other foods because your gut is healing from the damage and your body needs to reset. I find that keeping a food diary  and only slowly introducing other foods back into your diet over time is helpful. It is frustrating to feel so limited, but give it some time and patience. It can take the gut years to fully heal in many cases. 
    • Blue Roan
      Hi there, I am 30 and was diagnosed with celiac almost a year ago after a series of severe “unexplained” abdominal episodes. Everything is improving and I am feeling so much better overall except my cycle is worse. Has anyone else had a similar experience?  I got my period as a pre-teen and my cycles have been regular for as long as I can remember: every 21 days, lasting 5 days. My periods were heavy and I always had severe cramping at the start that subsided after the first two days.  I went gluten-free immediately when I was diagnosed in February. At first, my cycles were the same but around July, I started noticing very crazy symptoms around that time of the month: chills all over the body, severe headaches, some hot flashes, dry mouth and then cramps starting a few days earlier than usual. My cycles also started happening later and later. This time around, I’m on Day 35 and no period so far, but still cramping/abdominal pain/nausea on and off for the past week. It has been feeling like it’s about to happen any minute but nothing. I even get the pelvic contractions/pains but nothing after. I cannot sleep from all the hormonal fluctuations and chills. I can confirm I am not pregnant.  I’ve seen the endocrinologist, OBGYN, primary, and multiple gastro doctors throughout the year. No IBD ( but possible IBS), thyroid panel normal, thyroid ultrasound normal, negative for Hashimoto’s. I had a full vitamin panel and all levels normal (no anemia or vitamin B deficiency). After some testing, the gyn thinks PCOS is highly unlikely and that my body is “still adjusting” to going gluten-free. I’ve been strict gluten-free for nearly a year though.   All of my regular labs are normal and my antibodies are on a downward trend. I am really confused because more of my research points to the gluten-free diet resulting in better cycles rather than the opposite. While my cycles are not as heavy, they’re more unpredictable and uncomfortable with all these new symptoms. 
    • Mari
      Hi Emily, What you described is very similar to what I experienced in coping with Celiacs. I think my first symptoms started when I was about 3 and I wasn't diagnosed until I was almost 70. I got along OK util I was about 30  when I began to have more problems that the Drs thought was an autoimmune problem that they couldn't identify. Then I worked in medical labs in Bolivia for 8 months and returned to the US with more problems such as sensitivities to chemicals and increasing food intolerances. I had always had canker sores in my mouth and nose but have not had any now  since I went strictly gluten free. Before I was gluten-free I became very sensitive to hot peppers and then I could not eat anything spicy such as cinnamon, turmeric or black peppers. I have not eaten any nightshades for years. No corn or soy.  My diet now is lamb stew with rice, squash, green beans, chard, kale, collards with salt. Then eggs , chard, spinach, black beans, summer squash, asparagus, rice and salt. I eat peanuts for snacks. I have been eating nuts but may have to stop. Coconut is OK but too much sugar is not.  I am very cautious about adding back foods to my diet but hope to add back small amounts of turmeric. Take care.
×
×
  • Create New...