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

Kraft Creamy Ranch Dip For Chips? Gluten Free?


Jnkmnky

Recommended Posts

Jnkmnky Collaborator
:ph34r:

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



Celiac.com Sponsor (A8-M):



Jnkmnky Collaborator
:ph34r:
RiceGuy Collaborator

I don't think you trained him too well at all. I only wish I had known early on. Things would be far better for me.

All I found on the Kraft site was their PDF file on gluten-free products, basically saying to read the labels carefully :(

I like just plain sour cream with my chips, if anything.

Here's a link to some gluten-free sour cream, which is the base for most dips AFAIK.

Open Original Shared Link

They also have some flavored dips on their new products page:

Open Original Shared Link

Their rice ones are also soy free, but I believe casein is in all of them.

...Bonding over gluten on Thanksgiving

Heh, very funny.

2Boys4Me Enthusiast

Open Original Shared Link

for Kraft Canada, not sure about the U.S. link.

Jnkmnky Collaborator
:ph34r:
Guest nini

we've gotten the Kraft Creamy Ranch Dip here... Chey eats it without any problems. I haven't tried it though, I'm more sensitive to processed foods, so I try to avoid them.

KaitiUSA Enthusiast

Remember that Kraft is a brand that will not hide anything and will clearly list wheat, rye, barley, oats on the label if it contains any.


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



Celiac.com Sponsor (A8-M):



lovegrov Collaborator

"All I found on the Kraft site was their PDF file on gluten-free products, basically saying to read the labels carefully..."

What else do you hope to find? Kraft has one of the best ingredient policies of any company.

richard

Jnkmnky Collaborator
:ph34r:
Guest nini
Yeah, I know. Except that part in the policy where they refuse to spend the extra money on the bright red ink to write: GLUTEN FREE

underneath the ingredients of each product. I like the companies that do THAT..the best.

I HEAR YA!!!!!! I prefer to support companies that do this.

lovegrov Collaborator

I simply don't see the difference. Even when a company puts gluten free on a label, I read the ingredients. It's just second-nature now. And most companies that do put gluten-free on a label don't test it, so they're no more sure than Kraft is.

richard

Jnkmnky Collaborator
:ph34r:
Lisa Mentor

What richard says is correct, but I also understand your misgivings. When you are learning to read lables and doing your research it does get very confusing. There are often very big words regarding ingrediences that you don't know what they are.

The best thing to to is to do a search here on the site and study, study, study. Nine times out of ten your question has been asked and it can be searched here. Get your masters in reading ingrediences. I assure you that it will get better.

Keep on plugging along. There is light at the end of the tunnel.

I have been here for almost five months and I have learned an enormous amount of information, and I feel, that I am just beginning. Our time is just as valuable as yours, but we are all the same here.

Keep on.

Lisa B. ;)

Jnkmnky Collaborator
:ph34r:
Rachel--24 Collaborator
I simply don't see the difference. Even when a company puts gluten free on a label, I read the ingredients. It's just second-nature now. And most companies that do put gluten-free on a label don't test it, so they're no more sure than Kraft is.

richard

as you stated....they don't test the products. For this reason I would not only like to see the words GLUTEN-FREE but also MADE IN A DEDICATED FACILITY WITH NO CHANCE OF CROSS-CONTAMINATION 100% GUARANTEED.

THAT would make me really happy. Do you think thats asking too much? If I saw those words I would buy the product....I dont even care what it is....it would go right into my cart. :D

jerseyangel Proficient

Those are the magic words for me, too :)

Lisa Mentor

We all wish for that. In the days that I have spend hours in the grocery store I have realized that more and more product do present with "gluten free" and it is a joy to buy it. I have so much in my pantry that I bought, just because it said gulten free. I may not even have the need for it. But, you do have to understand that we are the underdogs here, but with a big voice. Change comes slowly. Maybe the next five years will be wonderous for us, but for now checking ingredience is a must.

The best way to change the labeling issue is to continually e-mail or call on 800 numbers and tell them that there are many of us here and without lableing their produces better we will not consume.

Write and e-mail as many producers as we are able.

We have dollars to purchase their products, let them know that we will buy them if they indicate that they are safe for us to purchase.....the old supply and demand. Well..........let's make it demand and then they will supply.

How about that. :):)

Lisa B.

psawyer Proficient

The problem with "gluten free" on a label is that, in today's world where whatever happens to you is never your fault, but always someone else's, lawsuits are likely. Even if a food is produced on dedicated lines or in a "gluten free" facility, cross contamination is always a possibility even if slight. No mainstream food maker produces all its own ingredients, and even if they did, how can you be 100% certain that a bee did not carry wheat pollen from another farmer's field and deposit a tiny amount of it on your corn? Even when the label DOES say "GLUTEN FREE" I realize the there is some possibility that contamination has occurred. I don’t let it ruin my life.

I am grateful for companies like Kraft (and many others) who label honestly and will not hide any gluten behind ambiguous ingredients. CYA disclaimers are a fact of life in this litigious society.

lovegrov Collaborator

As pointed out, there's no 100 percent guarantee. There might be places that are very close to 100 percent, but unless you control the production of every ingredient and every ingredient that goes into every ingredient and so on, there's ALWAYS a chance of CC.

And even then mistakes can happen. I think I even remember Kinnikinnick calling something back because of a possible error, and this is a company that doesn't allow its employees to bring gluten in their lunches. I also know that in the past they've stopped making products temporarily when they couldn't find an ingredient that met their guarantee criteria.

richard

ravenwoodglass Mentor
Yeah, I know. Except that part in the policy where they refuse to spend the extra money on the bright red ink to write: GLUTEN FREE

underneath the ingredients of each product. I like the companies that do THAT..the best.

At this point there is great debate about what defines gluten-free. That is one of the main reasons so few companies are doing this. The FDA is in the process of determining what levels define gluten-free. Do we use the European Standard, do we use one lower, do we use a 0 level policy? The European Standard may not be safe for American Celiacs as we tend to be diagnosed much later with more damage, wake up doctors. From what I understand this 'debate' should be over in a couple of years, they are aiming for 2008 as a date when gluten labeling regulations should be in effect. I'm just happy at least they are making clearer labels with more info. That damn term 'modified food starch' at least in 2006 they have to tell us what it is!

I love those gluten free labels we can already find, and hopefully we'll get lots more soon.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,843
    • Most Online (within 30 mins)
      7,748

    Lisa Harrison
    Newest Member
    Lisa Harrison
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.4k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, @Dawn Meyers! Are you currently on immunosuppressant medications for your various autoimmune disorders?
    • Dawn Meyers
      Hi I have celiac disease and the dermatitis herpetiformis rash Also other autommune diseases.  I have had bad side effects to all the vaccines I have had and now my Doctor wants me to have the pneumonia vaccine.  I am concerned because of some of the bad side effects I have had in the past example Hep B after shot couldn't  move arm for several months.  Flu shot and COVID was sick right after shot. Told not to get anymore. My lung is inflamed and have a cough I can't seem to get rid of. Very concerned 😟. 
    • knitty kitty
      @Manaan2,  I'm so happy to hear you're going to try thiamine and magnesium!  Do let us know the results!   You may want to add a B 50 Complex with two meals of the day to help boost absorption.  Thiamine interacts with each of the other B vitamins which are all water soluble.   When supplementing magnesium, make sure to get sufficient calcium.  Calcium and magnesium need to be kept in balance.  If you choose a calcium supplement, take two hours apart from magnesium as they compete for absorption.  Take Calcium with Vitamin D.  Vitamin D helps calm the immune system.   For pain, I use a combination of thiamine, B12 Cobalamine, and Pyridoxine B6.  These three vitamins together have analgesic effects.  My preferred brand is "GSG 12X Takeda ALINAMIN EX Plus Vitamin B1 B6 B12 Health Supplementary from Japan 120 Tablets".  Alinamin is another form of thiamine.  It really is excellent at relieving my back pain from crushed vertebrae without side effects and no grogginess.   Look into the low histamine version of the Autoimmune Protocol Duet (Dr. Sarah Ballentyne, a Celiac herself, developed it.)  It really helps heal the intestines, too.  It's like a vacation for the digestive system.  Add foods back gradually over several weeks after feeling better.   I'm so happy to have pointed the way on your journey!  Let us know how the journey progresses! P. S. Add a Potassium supplement, too.  Potassium is another electrolyte, like magnessium, that we need.
    • Manaan2
      @knitty kitty I can't thank you enough!  My husband and I already started looking into those supplements.  We definitely plan to give it a try.  We've been against the Miralax since it was originally advised by PCP, but because of the level of pain she experienced on a daily basis, we decided to try it.  We've made many attempts to gradually decrease but due to her pain and related symptoms, we've kept her on it while trying all sorts of other dietary adjustments pre and post diagnosis specific to food; so far none of those efforts have made a significant difference.  I will definitely share how she's doing along the way!
    • BIg Nodge
      Hi, I have recently embarked on the gluten-free journey. I have what to me seems like a somewhat confusing set of test results and symptoms. I have been impressed by the accumulated knowledge and thoughtfulness as I browse this forum, so I figured I'd make a post to see if anyone can offer any insight. I know there are many posts like this from new users, so I have tried to do my baseline research first and not ask super obvious questions.  I'm 43, overall very healthy. No history of gluten sensitivity or really any of the classic GI symptoms. About three years ago I started to experience intermittent bouts of fatigue, chills/cold intolerance, and shortness of breath/air hunger (sometimes feels like a hollowness in my chest, hard to describe). The symptoms over time have become fairly significant, though not debilitating, I am able to exercise regularly and am fairly physically active, continue to perform well at work. But for example I have gone from someone who consistently ran hot, was always cranking the a/c, to someone who wears a down vest inside at work in winter and get chills if the a/c even blows on me in summer. I get tired and lose energy even when getting decent amounts of sleep, and have to have my wife take over on long drives that I could previously handle with no problems. More generally when I am experiencing these symptoms they seem to crowd out space in my mind for focusing on my family, my hobbies/activities etc, I sort of withdraw into myself.   I happened to be experiencing these symptoms during an annual physical with my PCP a few years ago, he observed post nasal drip and suggested it was allergies and that I treat it with claritin. At first it seemed to respond to claritin (though not zyrtex), but over time I became unsatisfied with that answer. There didn't seem to be any seasonal rhyme or reason to my symptoms, and I felt like I was on an endless loop of taking claritin, then stopping, not being sure if it was even making a difference. I did eventually get allergy tests and found modest allergies to dust and pollen, which didn't feel like a smoking gun.  I then started seeing a natural medicine doctor who was much more willing to explore my symptoms via testing. The first thing that came back abnormal was elevated thyroid peroxidase antibodies/TPOs, 137 IU/mL vs a reference range of <9. At the same time my thyroid panel showed normal thyroid hormone levels. So it appears my immune system is attacking my thyroid even though it is working fine. I got a thyroid ultrasound at the time, it was clear, but with some abnormalities such that they suggested I get is scanned again in a year. These are certainly risk factors for a thyroid autoimmune disease, though my thyroid seems to be working fine for now.  From here my doctor considered celiac due to the murky thyroid/celiac links, so we did a panel. Results were as follows: TT IGA <1 U/ml, TT IGG <1 U/ml, deamidated gliadin IGA 24.6 U/ml, deamidated gliadin IGG <1 U/ml, IGAs 170 mg/dL. Readings greater than 15 considered high by my lab for the first four, my IGAs are within reference range. So basically just the deamidated IGA popped, but my IGAs are normal. I also notice on the tests that my thyroglobulin was high, 86.7 ng/ml vs a range of 2.8 - 40.9.  My doctor suggested that it certainly wasn't conclusive for celiac, but it was possible, and likely that I have some sort of gluten sensitivity. She suggested going gluten free and seeing how I felt as opposed to doing a biopsy. The best theory I can come up with is perhaps I am a silent celiac or just have a gluten sensitivity that doesn't produce immediate GI symptoms, but is still doing damage and over time has caused leaky gut. So now gluten is getting into my blood, and my immune system is attacking it but also mistakingly attacking my thyroid.  So that's what I did, went gluten free in October. It's been about four months, and I am really not feeling any difference. I still get the same symptoms that come and go. My bowel movements may be a bit more regular, but it was never a major issue before so I would consider that a minor improvement. I know that it can take a while to see improvements, and I am going to remain gluten-free and see how I feel. But I am definitely questioning whether I really understand what is going on, and am open to any thoughts or suggestions from the forum. Sometimes I wish I just went ahead with the biopsy before going gluten-free. While I would certainly be down to start drinking IPAs again ahead of a biopsy, you know, for science, I feel like at this point I would be throwing away four months of work and am better off staying the course and seeing what happens. But I'm really not sure.  I know there is a lot of thyroid knowledge on these boards, along with the celiac expertise, so I'm curious if this resonates with anyone's experience. And I'm interested in what sort of timelines people have experienced in terms of feeling improvements for some of these non-GI symptoms like chills, SOB, brain fog etc. Thanks in advance. 
×
×
  • Create New...