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 Dinner Cheese Packets

Canadian Karen

Recommended Posts

Canadian Karen Community Regular
Canadian Karen
Posted

but I haven't been able to find them anywhere up here in Canada. Are there any Canadians that can tell me if they have found them up here? I want to start putting Connor on more gluten-free items slowly, but I have to do it where he really doesn't realize at first. I can use gluten-free noodles, but you can't replace the taste of KD cheese packets!

Thanks!

Karen

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

Celiac.com Sponsor (A8-M):


Lisa Mentor
Lisa
Posted

I'll send you some as well a some lea & perrins worcestershire sauce if you would like, but the postage, not your continues source.

xo

2Boys4Me Enthusiast
2Boys4Me
Posted

Hi Karen,

Check your grocery in the cheese section near the Kraft grated Parmesan in the green shaker. In or around that area should be a similar Kraft product called grated Cracker Barrel cheese. It's in an orangey-yellow shaker. My kids say it tastes pretty much the same.

http://www.kraftcanada.com/en/ProductsProm...ratedCheese.htm

StrongerToday Enthusiast
StrongerToday
Posted

I found some at on on-line grocer (I googled "kraft cheese powder") and got some in a can that's meant to be sprinkled on popcorn, etc. It's the real thing, thank GOd :lol: Someone else mentioned to me that since a box is really so cheap, why not just throw out the noodles and use the cheese package? Or could that be a cc issue for you?

TrillumHunter Enthusiast
TrillumHunter
Posted

Hi,

My in-laws buy that stuff at a bulk foods place. I've seen it online from bulk suppliers. Look for popcorn cheese. I've also found it at Wal-Mart in a small can that looks just like the blue box. It is with the canned parmesan cheese. I don't know if they have Cabot cheese in Canada but they make a some called Cheddar Shake. It isn't orange though :P

Monica

mamatide Enthusiast
mamatide
Posted
but I haven't been able to find them anywhere up here in Canada. Are there any Canadians that can tell me if they have found them up here? I want to start putting Connor on more gluten-free items slowly, but I have to do it where he really doesn't realize at first. I can use gluten-free noodles, but you can't replace the taste of KD cheese packets!

Thanks!

Karen

Hi Karen - I too have been looking for the sauce mix (I usually buy a box of Kraft Dinner and throw out all but the cheese package, substituing Tinkykada pasta).

I found this at amazon .com

http://www.amazon .com/Kraft-Macaroni-and-C...g/dp/B000I60JUW

looks like the stuff they're talking about above?

  • 11 years later...
AmandaPanda420 Newbie
AmandaPanda420
Posted

I bought the regular boxes of Kraft mac n cheese and threw out the noodles just to use the cheese with my gluten free noodles and it messed up my stomach bad. I even tried it twice to make sure it was the cheese that messed me up so bad ? It was just so good that I figured I should try again to make sure it was the culprit lol

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

Celiac.com Sponsor (A8-M):


Ennis-TX Grand Master
Ennis-TX
Posted
2 hours ago, AmandaPanda420 said:

I bought the regular boxes of Kraft mac n cheese and threw out the noodles just to use the cheese with my gluten free noodles and it messed up my stomach bad. I even tried it twice to make sure it was the cheese that messed me up so bad ? It was just so good that I figured I should try again to make sure it was the culprit lol

Could also be the dairy or any of the other crud in the cheese....I make my own vegan cheese sauces, or buy a Alfredo cashew cheese sauce I recently found. Daiya makes their cheese packets you can just buy to put on what ever you wish. Many celiacs have issues with dairy as the damaged villi will not work with the enzymes to break it down.
Open Original Shared Link
Open Original Shared Link
Open Original Shared Link

pschwab Enthusiast
pschwab
Posted

Annie’s brand cheese in the gluten-free boxed Mac and cheese is pretty good. We buy that, throw out the gross rice noodles and substitute barilla gluten-free elbows. My kids love it. Maybe they have that in Canada?

Nikki2777 Community Regular
Nikki2777
Posted

Trader Joe's Rice Pasta Mac n Cheese is pretty close, cheese-wise. The noodles are ok, if a little thin.

Archived

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

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


  • Member Statistics

    • Total Members
      126,112
    • Most Online (within 30 mins)
      7,748
    cam4180
    Newest Member
    cam4180
    Joined
  • Celiac.com Sponsor (A20):

  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.2k
  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • StaciField
      My bone structure is disintegrating and I’m having to have my teeth removed

      By StaciField · Posted

      There’s a Cosco in Auckland in New Zealand. It’s a bit away from where I live but it’s worth the travel for me. Very appreciative of your advice.
    • Wheatwacked
      Celiac Maybe a Possibility?

      By Wheatwacked · Posted

      It seems you have proven that you cannot eat gluten.  You've done what your doctors have not been able to do in 40 years. That's your low vitamin D, a common symptom with Celiac Disease.  Zinc is also a common defiency.  Its an antiviral.  that's why zinc gluconate lozenges work against airborne viruses.  Vitamin D and the Immune System+ Toe cramps, I find 250 mg of Thiamine helps.   When I started GFD I counted 19 symptoms going back to childhood that improved with Gluten Free Diet and vitamin D. I still take 10,000 IU a day to maintain 80 ng/ml and get it tested 4 times a year. Highest was 93 ng/ml and that was at end of summer.  Any excess is stored in fat or excreted through bile.   The western diet is deficient in many nutrients including choline and iodine.  Thats why processed foods are fortified.  Celiac Disease causes malabsorption of vitamins and minerals from the small intestine damage.  GFD stops the damage, but you will still have symptoms of deficiency until you get your vitamins repleted to normal.  Try to reduce your omega 6:3 ratio.  The Standard American Diet is 14:1 or greater.  Healthy is 3:1.  Wheat flour is 22:1.  Potatoes are 3:1 while sweet potatoes are 14:1.  So those sweet potatos that everyone says is better than Russet: they are increasing your inflammation levels.   
    • Scott Adams
      Weird Symptoms

      By Scott Adams · Posted

      My mother also has celiac disease, and one of her symptoms for many years before her diagnosis was TMJ. I believe it took her many years on a gluten-free diet before this issue went away.
    • Jeff Platt
      Weird Symptoms

      By Jeff Platt · Posted

      Ear pain and ringing your entire life may or may not be TMJ related but could be something else. A good TMJ exam would be helpful to rule that out as a potential cause from a dentist who treats that. I have teens as well as adults of all ages who suffer from TMJ issues so it’s not a certain age when it shows up.   
    • cristiana
      Weird Symptoms

      By cristiana · Posted

      Not sure if related to coeliac disease but my ear ringing  has stepped up a notch since diagnosis.  Even since a child silence really hurts my ears - there is always a really loud noise if there is no other noise in a quiet room - but my brain has learned to filter it out.  Since diagnosis in my forties I also get a metallic ringing in my ears, sometimes just one, sometimes both.  But it comes and goes.   My sister also suffers now, we are both in our fifties, but she is not a coeliac, so for all I know it could just be an age thing.  I do get occasional stabbing pain in my ears but that has been all my life, and I do appear to be vulnerable to outer ear infections too.  So not a particularly helpful reply here, but I suppose what I am trying to say is it might be related but then again it could just be one of those things.   I think in the UK where I live doctors like you to report if you get tinnitus in just the one ear.  I reported mine but no cause was found.  Most of the time it is nothing but sometimes it can have a cause that can be treated, so perhaps worth reporting to your GP.  
×
×
  • Create New...