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

I Thought Gluten-Free Eating Would Be Healthier!


Monklady123

Recommended Posts

Monklady123 Collaborator

So -- I went browsing through the grocery store again today and made a discovery. I had thought that gluten-free would be healthier since I'll be cooking more from scratch. Well... discovered my VERY favorite junk food, Utz ripple cut potato chips, is gluten-free! woot! And what was my very first thought? Not "oh really, these are not good for me".. but instead it was "oh wow, and since I can't eat bread or my favorite crackers etc. any more I can just eat more potato chips." hmmm.. somehow this may not be a good thing. :rolleyes:


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



Celiac.com Sponsor (A8-M):



kayo Explorer

I have eaten my fair share of potato chips and then some! I'm glad to have a crunchy and salty comfort food that can be found anywhere. If you can't find Utz try Lays Wavy. They're what I would call a classic ruffle potato chip. To offset the chips just have a bit more broccoli :D

Fey Rookie

I said my goal was to find as many junk food items as possible that were gluten free. It's the only way to keep me from bawling every time I open the pantry and see Oreos.

I am eating much healthier (cooking from scratch vs hamburger helper or burgers/hot dogs for dinner), but it's also a relief to know there's a wide range of easily found snacks that I can get in a pinch. Cheetos, soda, lay's, LARABAR fruit bars (the banana ones are delish, and it's dairy/soy/gluten free), fruits, certain candy bars, etc.

Monklady123 Collaborator

I have eaten my fair share of potato chips and then some! I'm glad to have a crunchy and salty comfort food that can be found anywhere. If you can't find Utz try Lays Wavy. They're what I would call a classic ruffle potato chip. To offset the chips just have a bit more broccoli :D

Good tip Kayo... every piece of broccoli I have cancels out a bunch of chips. Right? B)

Northern Celiac Newbie

Just because it's gluten free doesn't mean it's good for you. I learned that the hard way

Skylark Collaborator

Learning Snickers is gluten-free was not necessarily a good thing for me. :P

Monklady123 Collaborator

Learning Snickers is gluten-free was not necessarily a good thing for me. :P

Ooooooooooh, Snickers! yummmm.......... :D


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



Celiac.com Sponsor (A8-M):



dakota girl Rookie

Ditto @ the Snickers! They are my guilty indulgence! I have a hard time passing up a Frito, too! But, many times I'm on a plate of raw vegies w/Sam's Club gluten-free Ranch Dressing...yummy, in a better way!

ravenwoodglass Mentor

Learning Snickers is gluten-free was not necessarily a good thing for me. :P

Snickers are a wonderful treat!

My DD literally jumped for joy when we discoved they were safe. She even wrote her entrance essay for college on the 'ritual' she did to eat them. That ritual was quite a process and rather fun to watch as she would use a knife and fork. Not only did she get in but she also easily got her own room in senior housing her freshman year so she had her own kitchen.

anabananakins Explorer

My response to being unable to eat takeaway anymore has been to eat baked potatos with heaps of butter every night. It's not healthy but knowing I can still have the delicious taste of melted butter on something has gone a long way to soothing the pain of losing bread, lol. Maybe I could have my melted butter with broccoli instead, hmmmm.

Takala Enthusiast

I said my goal was to find as many junk food items as possible that were gluten free. It's the only way to keep me from bawling every time I open the pantry and see Oreos.

I am eating much healthier (cooking from scratch vs hamburger helper or burgers/hot dogs for dinner), but it's also a relief to know there's a wide range of easily found snacks that I can get in a pinch. Cheetos, soda, lay's, LARABAR fruit bars (the banana ones are delish, and it's dairy/soy/gluten free), fruits, certain candy bars, etc.

____________________

You haven't found the K- Toos yet, I take it ?

Open Original Shared Link

BlackSillyYack Newbie

____________________

You haven't found the K- Toos yet, I take it ?

Open Original Shared Link

I ate healthy and did heavy body building BEFORE I got sick.

I was 245 with low body fat 18 months ago. I am a very sickly 170 today.

for the life of me it seems like this disease just HAPPENED all at once. but where as I used to eat nothing but meat and more meat. now all I eat (if I ever eat) are bad things. I have basil fried rice (without soy sauce) almost every day of the week. I have baked THREE betty crocker cakes in the past week and a half, I have a cabinate full of gluten free cookies, and constantly eat a cup o noodles (thai rice noodle gluten free) every night.

I am glad I dont live any place close to where I did before, because the people I used to go to the gym with would disown me. but, I dont care at this point I am just trying to stay alive.

GFinDC Veteran

Well, I am not perfect in that regard either. I used to eat those Starburst fruit chews things because they are one of the few gluten-free things I could find in a convenience store without any dairy or soy. Basically a bunch of corn syrup, sugar and flavoring chemicals. No more though.

Then I found Corn Nuts by Kraft. Corn, corn oil, salt, at least in the orginal flavor. I still like to grab those sometimes when I find them.

Then just yesterday I decided to finally try some Skittles since I kept reading on here that they are gluten free. Yeesh, nothing but sugar and junk. Way too sweet. So then Yahoo health put out a nice article today on what is bad about food and they spotlight Skittles as crap food. I think they are right there. I'd read before that Skittles have lac in the coating but I don't see that in the ingredients. Lac is what they make shellac from.

Open Original Shared Link

Hey all, if you want to avoid the junk, try going dairy free, soy free and nightshade free too. Most of the gluten-free treats have one or more of those in them.

Larabars, now those are ok.

I did find some Planters brand peanut bars the other day that are gluten-free.

Welcome to our wonderful club BSY!

curlyfries Contributor

I ate healthy and did heavy body building BEFORE I got sick.I was 245 with low body fat 18 months ago. I am a very sickly 170 today. for the life of me it seems like this disease just HAPPENED all at once. but where as I used to eat nothing but meat and more meat. now all I eat (if I ever eat) are bad things. I have basil fried rice (without soy sauce) almost every day of the week. I have baked THREE betty crocker cakes in the past week and a half, I have a cabinate full of gluten free cookies, and constantly eat a cup o noodles (thai rice noodle gluten free) every night.I am glad I dont live any place close to where I did before, because the people I used to go to the gym with would disown me. but, I dont care at this point I am just trying to stay alive.

I am confused why you are no longer eating meat. Do you have other food issues as well? How long have you been gluten-free?

Are you feeling better eating the way you are now?

Perhaps you should start trying to add some healthier foods now......vegetables, beans, almond butter, eggs (trying to think of protein replacement)

I can't have sugar in any form. So...no fruit, grains, snacks. Very boring. I recently went to a new free clinic through my job to deal with some other health issues i had been putting off and did not even think to mention this problem and the possibility of candida, bacterial overgrowth.....whatever. I am so used to living this way :P

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,266
    • Most Online (within 30 mins)
      7,748

    Cindy Whitis
    Newest Member
    Cindy Whitis
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.8k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Sorry but I don't have specific recommendations for doctors, however, starting out with good multivitamins/minerals would make sense. You may want to get your doctor to screen you for where you different levels are now to help identify any that are low, but since you're newly diagnosed within the past year, supplementation is usually essential for most celiacs.
    • trents
      Yes, I can imagine. My celiac journey started with a rejection of a blood donation by the Red Cross when I was 37 because of elevated liver enzymes. I wasn't a drinker and my family doctor checked me for hepatitis and I was not overweight. No answers. I thought no more about it until six years later when I landed a job in a healthcare setting where I got annual CMP screenings as part of my benefits. The liver enzymes were continually elevated and creeping up every year, though they were never super high. My primary care doc had no clue. I got really worried as your liver is pretty important. I finally made an appointment with a GI doc myself and the first thing he did was test me for celiac disease. I was positive. That was in about 1996. After going on a gluten-free diet for three months the liver enzymes were back in normal range. Another lab that had gotten out of whack that has not returned to normal is albumin/total protein which are always a little on the low side. I don't know what that's about, if it's related to the liver or something else like leaky gut syndrome. But my doctors don't seem to be worried about it. One thing to realize is that celiac disease can onset at any stage of life. There is a genetic component but there is also an epigenetic component. That is, the genetic component is not deterministic. It only provides the potential. There needs also to be some health or environmental stressor to activate the latent gene potential. About 40% of the population have the genetic potential to develop celiac disease but only about 1% actually do.
    • cristiana
      Hello @Heather Hill You are most welcome.  As a longstanding member and now mod of the forum, I am ashamed to say I find numbers and figures very confusing, so I rarely stray into the realms of explaining markers. (I've self-diagnosed myself with dyscalculia!)  So I will leave that to @Scott Adams or another person. However as a British person myself I quite understand that the process with the NHS can take rather a long time.  But just as you made a concerted effort to eat gluten before your blood test, I'd advise doing the same with eating gluten before a biopsy, in order to show if you are reacting to gluten.  It might be worth contacting the hospital or your GPs secretary to find out if they know what the current waiting time is. Here is a page from Coeliac UK about the current NHS recommendations. https://www.coeliac.org.uk/information-and-support/coeliac-disease/getting-diagnosed/blood-tests-and-biospy/#:~:text=If you remove or reduce,least six weeks before testing. Cristiana  
    • MI-Hoosier
      Thanks again. My mom was diagnosed over 50 years ago with celiac so grew up watching her deal with the challenges of food. I have been tested a few times prior due to this but these results have me a bit stunned. I have a liver disease that has advanced rapidly with no symptoms and an allergy that could be a contributing factor that had no symptoms. I guess I’ll call it lucky my Dr ordered a rescreen of a liver ultrasound from 5 years ago that triggered this or I would likely have tripped into cirrhosis. It’s all pretty jarring.
    • Heather Hill
      Many thanks for your responses, much appreciated.  The tests did include tTg IgA and all the other markers mentioned.  I also had sufficient total IgA so if I'm reading the Mayo clinic thing correctly, I didn't really need the anti-deaminated gliadin marker? So, if I am reading the information correctly do I conclude that as all the other markers including tTg IgA and DGP IgG and tTg IgG and EMA IgA are all negative, then the positive result for the immune response to gliadin, on it's own, is more likely to suggest some other problem in the gut rather than Coeliac disease? Until I have a view from the medics (NHS UK) then I think I will concentrate on trying to lower chronic inflammation and mend leaky gut, using L glutamine and maybe collagen powder. Thank you for your help so far.  I will get back in touch once I have a response, which sadly can take quite a long time.   Kindest Heather Hill 
×
×
  • Create New...