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

List of Brands: Certified gluten free with SHARED LINES


mama.liz07

Recommended Posts

mama.liz07 Apprentice
(edited)

FYI!

 

Certified gluten free foods (tested below 10ppm) are often made on shared equipment. 
Also, foods labeled gluten free (tested below 20ppm) can also be made on shared equipment. 

Cumulatively, this could be too much gluten.
i.e. If you use too many brands that all contain trace amounts of gluten then you could accumulate too much gluten, even if the individual product amounts are below accepted levels.

Brands that use Shared Lines
(gluten foods made on the same equipment as gluten-free foods)

 

Alter eco chocolate
Amy’s
Arrowhead
Bird's Eye frozen veggies
Blakes shepherd pies
Bolthouse Farms
Breyers ice cream
Classico
Color kitchen cupcake colors
Conagra
Country life vitamins
Drews
Erewhon
From the ground up
Gin Gins
Grandy oats
Haagen-Dazs
Hellman's
Imagine Foods
Jeff's Natural Jalapeno stuffed olives
Kind
Kraft foods
Lance
Late july
Lotus Foods
Lovely Candy company
Nature's Bakery
Nature’s Path
Nestle
Organic Valley
Orrington farms broth
Outshine popcicles
Pacific Foods
Purdue/Harvestland Chicken
San-j
Simple Mills
Stubbs
Unilever
Vans
Wild Planet fish
Natural Sea Salmon
So-delicious

 

**NOTE**
This is not an exhaustive list. My information is only as good as the representative with whom I spoke.  This list is time sensitive.
However, I am FINALLY getting well after cutting out ALL brands that use shared lines! 


 

 

Edited by mama.liz07
Correction from another member.

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



Celiac.com Sponsor (A8-M):



kareng Grand Master
21 minutes ago, mama.liz07 said:

FYI!

 

Certified gluten free foods (tested below 10ppm) are often made on shared equipment. 
Also, foods labeled gluten free (tested below 20ppm) can also be made on shared equipment. 

Cumulatively, this could be too much gluten.
i.e. If you use 5 brands and each has between 5-15 ppm of gluten then you are over the safe limit.

 

 


 

That’s not how it works.  You don’t eat 3 foods and add the ppm.  Also, less than ten ppm could mean 0.  Parts  per million is easier to think of like a percentage- it’s ppm of the total food you eat at once.  if everything is under 20 ppm, it’s gluten-free.  

 

mama.liz07 Apprentice

Well, that's good to know.  But I sure have been getting sick on shared equipment foods.  When I looked at the regulations--how often they have to test, how large the sample is, etc, I think there could be parts of the food that are higher and parts that are okay.  And they don't have to test every batch.  But whatever is happening, my son and I finally getting well.  Trading out shared lines foods for dedicated gluten free line foods.  Same types of foods, just different brands.  Might be helpful to others too.  But I'm just a celiac mama with a celiac son, definitely not an expert.  Take my list with a grain of salt!  And thanks for the info!

cyclinglady Grand Master
(edited)

@mama.liz07— 

I went grain free after I got my diabetes diagnosis (one year after my celiac disease diagnosis) to reduce carbs and I finally felt better.  What I realized that although my hubby could tolerate many processed gluten-free foods, I could not.  For example,  I have issues with Xanthan Gum.  While I am no longer lactose intolerant, I can not tolerate peppers or anything related to the garlic family.  While I healed from celiac disease, I still have issues with my other AI issues.  I think I am pretty sensitive and I have come to realize that 20 ppm might be okay for some celiacs but not others.  

We each need to find our own way.  For example, I use Stubbs for chili (it is certified gluten-free), I can not eat it.  I feed it to hubby and my kid.  It is gluten free, but the peppers and onions  make me ill.  

I avoid all processed oats (for hubby) because I can not be assured the oats are pure or mechanically sorted (General Mills made a huge investment and they need to sell bulk oats to all the little gluten-free food companies to offset that investment in my opinion).  

The gluten free Watchdog has tested most processed foods labeled gluten-free (e.g. Classico pasta sauce) and some not labeled gluten-free.    She found that the vast majority of manufacturers comply with FDA regulations.  I encourage you to subscribe.  She is like a mini Consumer Reports for gluten-free.  

Processed food is really junk — gluten free or not.  

I am glad you and your son are getting better! 

Edited by cyclinglady
mama.liz07 Apprentice
1 hour ago, cyclinglady said:

@mama.liz07— 

I went grain free after I got my diabetes diagnosis (one year after my celiac disease diagnosis) to reduce carbs and I finally felt better.  What I realized that although my hubby could tolerate many processed gluten-free foods, I could not.  For example,  I have issues with Xanthan Gum.  While I am no longer lactose intolerant, I can not tolerate peppers or anything related to the garlic family.  While I healed from celiac disease, I still have issues with my other AI issues.  I think I am pretty sensitive and I have come to realize that 20 ppm might be okay for some celiacs but not others.  

We each need to find our own way.  For example, I use Stubbs for chili (it is certified gluten-free), I can not eat it.  I feed it to hubby and my kid.  It is gluten free, but the peppers and onions  make me ill.  

I avoid all processed oats (for hubby) because I can not be assured the oats are pure or mechanically sorted (General Mills made a huge investment and they need to sell bulk oats to all the little gluten-free food companies to offset that investment in my opinion).  

The gluten free Watchdog has tested most processed foods labeled gluten-free (e.g. Classico pasta sauce) and some not labeled gluten-free.    She found that the vast majority of manufacturers comply with FDA regulations.  I encourage you to subscribe.  She is like a mini Consumer Reports for gluten-free.  

Processed food is really junk — gluten free or not.  

I am glad you and your son are getting better! 

Thanks for sharing!  I'm glad you've figured out what works for you too!  And I agree--I think most companies do a good job following the guidelines of the FDA, certification groups, etc.  I just didn't realize until recently how many of my products--even healthy ones like butter, chicken, frozen veggies, canned fruit, etc...are processed on shared lines. Trace amounts just seem to be too much for me, even if they are at accepted levels.  Gonna try the gluten-free facilities for a while...seems to be helping!!  ? 

Scott Adams Grand Master

Here is a much bigger list:

https://gluten.org/wp-content/uploads/2019/04/gfco-catalog-2018.pdf 

These are not necessarily on shared lines, but this is a list of certified gluten-free companies.

mama.liz07 Apprentice
35 minutes ago, Scott Adams said:

Here is a much bigger list:

https://gluten.org/wp-content/uploads/2019/04/gfco-catalog-2018.pdf 

These are not necessarily on shared lines, but this is a list of certified gluten-free companies.

Thanks! That is a massive list! 


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



Celiac.com Sponsor (A8-M):



Beverage Rising Star
On 5/16/2019 at 2:41 PM, kareng said:

That’s not how it works.  You don’t eat 3 foods and add the ppm.  Also, less than ten ppm could mean 0.  Parts  per million is easier to think of like a percentage- it’s ppm of the total food you eat at once.  if everything is under 20 ppm, it’s gluten-free.  

 

Everything I have read is that getting to the point of triggering an autoimmune response IS CUMULATIVE.  So 1 bit here, 1  there, 1 bit after, it adds up and then bam you have a reaction.  And some may react on less than others.  Moderators or those more experienced, please chime in.  Oh heck, I just did an internet search, and yes, it is cumulative.

On 5/16/2019 at 2:41 PM, kareng said:

That’s not how it works.  You don’t eat 3 foods and add the ppm.  Also, less than ten ppm could mean 0.  Parts  per million is easier to think of like a percentage- it’s ppm of the total food you eat at once.  if everything is under 20 ppm, it’s gluten-free.  

 

Everything I have read is that getting to the point of triggering an autoimmune response IS CUMULATIVE.  So 1 bit here, 1  there, 1 bit after, it adds up and then bam you have a reaction.  And some may react on less than others.  Moderators or those more experienced, please chime in.  Oh heck, I just did an internet search, and yes, it is cumulative.

kareng Grand Master
56 minutes ago, Beverage said:

Everything I have read is that getting to the point of triggering an autoimmune response IS CUMULATIVE.  So 1 bit here, 1  there, 1 bit after, it adds up and then bam you have a reaction.  And some may react on less than others.  Moderators or those more experienced, please chime in.  Oh heck, I just did an internet search, and yes, it is cumulative.

Everything I have read is that getting to the point of triggering an autoimmune response IS CUMULATIVE.  So 1 bit here, 1  there, 1 bit after, it adds up and then bam you have a reaction.  And some may react on less than others.  Moderators or those more experienced, please chime in.  Oh heck, I just did an internet search, and yes, it is cumulative.

That wasn't how experts have explained it to me/in seminars.  Please post your internet search.  Perhaps we are not talking about it in the same terms?

Beverage Rising Star

Cumulative throughout the day, not over a long period of time. Sorry for the confusion.

Scott Adams Grand Master

@Beverage I think with some people very tiny amounts even once can trigger a severe reaction, and with other people like myself it would take small contamination over time to add up and cause noticeable issues. Keep in mind however, just because small amounts of contamination may not trigger noticeable symptoms in some celiacs it does not mean that damage isn’t being done, or that there aren’t risks. Many celiacs have no obvious symptoms.

Beverage Rising Star

Thank you. All very good points. That's me, no intestinal symptoms but after a few weeks of unknowingly consuming gluten, I finally feel like I've been hit by a truck. We're all different.

cyclinglady Grand Master

“Understanding Less Than 20 Parts Per Million (PPM)

It is a common misconception that foods labeled "gluten-free" can or do contain zero parts per million (ppm) of gluten. At this time, no validated tests are able to accurately detect gluten at zero. Less than 20 ppm is an amount that has been deemed safe by celiac disease experts for MOST people living with the genetic autoimmune disease.

In 2011, Beyond Celiac Scientific/Medical Advisory Council Member Dr. Alessio Fasano of the Center for Celiac Research at Massachusetts General Hospital (formerly at the University of Maryland), wrote a letter called "In Defense of 20 Parts Per Million." In this letter, Dr. Fasano explains why this amount has been deemed safe for most people with celiac disease.” 

https://www.beyondceliac.org/gluten-free-diet/food-labeling-laws/

https://www.beyondceliac.org/SiteData/docs/InDefenseo/7a4890bd693bc562/In Defense of 20 ppm_Alessio Fasano Letter.pdf

https://celiac.org/about-the-foundation/featured-news/2014/08/fda-gluten-free-food-labeling-information-page/

Some people who have celiac disease may be more sensitive than others and 20 ppm might be too much for them.  We each have to determine our individual thresholds based on our needs.  There is no “one size fits all” gluten-free diet as we also tend to have individualized intolerances or other illnesses.  

This from the EU disputes that 20 ppm may be too much.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766553/

Whitepaw Enthusiast

When I was first diagnosed,  my Dr. said same line foods were not OK. 

mama.liz07 Apprentice
6 hours ago, Whitepaw said:

When I was first diagnosed,  my Dr. said same line foods were not OK. 

Mine did too and because of that, I just assumed certified foods would NOT be produced on shared lines.  I was very surprised to learn otherwise.

And for foods that say "gluten free" but aren't certified, when I called and asked about cross contamination, the companies often said, "there is no chance of cross contamination."  I assumed that meant dedicated lines.  I now understand that "no chance" often means they wash thoroughly and test.  (you have to get very specific with the way you ask your questions).  I'm sure shared lines (especially when certified) are fine for some people with celiac, but not for others.  I guess my son and I just happen to be the hypersensitive type. We are doing much much better only using products made on dedicated lines!

mama.liz07 Apprentice
14 hours ago, cyclinglady said:

“Understanding Less Than 20 Parts Per Million (PPM)

It is a common misconception that foods labeled "gluten-free" can or do contain zero parts per million (ppm) of gluten. At this time, no validated tests are able to accurately detect gluten at zero. Less than 20 ppm is an amount that has been deemed safe by celiac disease experts for MOST people living with the genetic autoimmune disease.

In 2011, Beyond Celiac Scientific/Medical Advisory Council Member Dr. Alessio Fasano of the Center for Celiac Research at Massachusetts General Hospital (formerly at the University of Maryland), wrote a letter called "In Defense of 20 Parts Per Million." In this letter, Dr. Fasano explains why this amount has been deemed safe for most people with celiac disease.” 

https://www.beyondceliac.org/gluten-free-diet/food-labeling-laws/

https://www.beyondceliac.org/SiteData/docs/InDefenseo/7a4890bd693bc562/In Defense of 20 ppm_Alessio Fasano Letter.pdf

https://celiac.org/about-the-foundation/featured-news/2014/08/fda-gluten-free-food-labeling-information-page/

Some people who have celiac disease may be more sensitive than others and 20 ppm might be too much for them.  We each have to determine our individual thresholds based on our needs.  There is no “one size fits all” gluten-free diet as we also tend to have individualized intolerances or other illnesses.  

This from the EU disputes that 20 ppm may be too much.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766553/

I checked out this last article and then linked from there to a study done by the FDA.  I thought this was interesting. 

"In sum, these findings indicate that a less than 1 ppm level of gluten in foods is the level of exposure for individuals with celiac disease on a GFD that protects the most sensitive individuals with celiac disease and thus, also protects the most number of individuals with celiac disease from experiencing any detrimental health effects from extended to long-term exposure to gluten."
https://www.fda.gov/media/81500/download

cyclinglady Grand Master

Wow!  That was a long report.  

Since my celiac disease diagnosis and becoming a member of celiac.com, I have realized that we are all unique.  How we react to gluten varies in terms of symptoms and the amount of gluten we can safely consume before setting off an autoimmune reaction.  The 20 ppm cut off set by celiac researchers was a start.  Perhaps, newer testing methods in the future may allow manufacturers to eventually get to zero ppm.  

My hubby was gluten free some 12 years before my diagnosis.  He went gluten free based on the advice of my allergist and his GP.  The diet worked.  He refuses to do a challenge and I can not blame him.  Back then, there was pretty much nothing processed that was gluten free except at health food stores and it was awful.   Instead, we chose foods that were naturally gluten free and minimally processed.  He thrived.  After my diagnosis, The switch to gluten-free was easy. I knew the drill.  A year after my diagnosis, I started having blood sugar issues.  So, I went on a low carb diet (basically ate to my meter).  By doing so, I gave up all grains (they spike my blood sugar).  Amazingly, I finally felt better.   Was it avoiding grains, less junk, or managing my diabetes?  Who knows? 

When I get an exposure to gluten, I get deathly ill.  Which is weird because at the time of my diagnosis, I was only anemic.   Days of vomiting, pain, diarrhea, bloating, and passing out occurs.  Then continued weeks of trying to digest anything.  The last time I triggered a bout of autoimmune hives for six months.  I was mess. 

I am so careful now.  Super strict.  I tend to follow the advice of DH sufferers.  I can not imagine having DH!  Being careful has paid off.  My small intestine has healed based on repeat biopsies.  My hubby is often not strict.  Oh, he never cheats, but he will consume gluten-free processed foods and eat at some not dedicated restaurants that I will not take a chance on.  Nothing is worth the risk of becoming so ill for me. He only gets ill for a week.    I have been glutened only at restaurants (vacations) and possibly through one medication that might not have been gluten free. (Funny how food manufacturers  must follow the FDA requirements, but not pharmaceutical companies. Call your representative today and get that bill passed this year!)  I am super careful about taking risks.  

Do what works for you and your family.  The goal is to heal and live a healthy life.  

 

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,289
    • Most Online (within 30 mins)
      7,748

    Chanel Moolman
    Newest Member
    Chanel Moolman
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Dora77
      Sorry for the long post. I’m 18, and I was diagnosed with celiac disease and type 1 diabetes (T1D). My transglutaminase IgA was >128 U/mL, EMA IgA positive twice, and I’m HLA-DQ2 and DQ8 positive. I’ve been completely asymptomatic since diagnosis, even when I cheated with gluten sometimes in the past and used to eat out(2-5 years ago) I don’t get the typical celiac reactions, which makes it really hard to know when (or if) I’ve been glutened. But for the past year, I’ve been the most strict with my diet, and that’s also when a bunch of new issues started. I eat completely glutenfree, never eat out, dont eat food that says „may contain gluten“.   Current Health Problems • Floating, undigested stools for over a year now. Dont think its related to celiac as it was like this since im 17 and not 13-16( i got diagnosed at 13). • Chronic back pain started gradually, worsens with movement, lots of cracking/popping sounds. Been ongoing for a year now. First noticed in the gym. • Abdominal bulge on the right side, not painful but seems to be getting slightly bigger. Doctor didn’t find a hernia on ultrasound, but it was done lying down (I’ve read those can miss hernias). Noticed it like 6 months ago, couldve been there longer. • extremely dry and mildly swollen hands (this started before I started excessive hand-washing), and bloated face. • Signs of inattentive ADHD (noticed over the past 3 years), now combined with severe OCD focused on contamination and cross-contact. • Growth/puberty seemed to started after going gluten-free. Before that I was not developing. Dont know if any of these are because of celiac as my dad doesnt have those and he is a lot less strict gluten-free then me. I also had pancreatic elastase tested four times: values were 46 (very low), 236, 158, and 306 (normal). Gastroenterologist said one normal value is enough and I don’t have EPI. Family doctor prescribed Kreon anyway (after I pushed for it), and I just started taking 1 capsule (10,000 units) with meals 2 days ago, but couldn‘t see effects yet because I’ve been constipated the last few days. Maybe because of thyroid. I don’t have Hashimoto’s. No thyroid antibodies. But I took levothyroxine for slightly low FT4 levels. My thyroid levels fluctuated between borderline low and low-normal. And recently lowered my dose so that may have caused the constipating. I probably didn’t need it in the first place, and am thinking about stopping it soon.   Current Diet Right now, I only eat a very limited set of “safe” foods I prepare myself: • Gluten-free bread with tuna or cheese • Milk and cornflakes • gluten-free cookies/snacks • Bananas (the only fruit I trust right now) I rarely eat other fruits or vegetables, because I’m scared of contamination. My dad, who also has celiac but doesn’t care about CC, buys fruits, and he might’ve picked them up right after handling gluten bread. That makes me feel unsafe eating them. Even fruit at stores or markets feels risky because so many people with gluten on their hands touch them.   My Home Situation (Shared Kitchen) We’re a family of 5. Only my dad and I have celiac. He eats glutenfree but doesn’t care about CC and sometimes (but rarely) cheats. My mom and siblings eat gluten bread at every meal. My mom is honest (so if i ask her to be cautious, she most likely would try to), but doesn’t seem to understand how serious celiac is. She: • Stopped using gluten flour • only cooks gluten-free meals (but they still heat up gluten bread and also cook gluten noodles) • Keeps separate butter/jam/jars for me • Bought me a stainless steel pan Bu we didn’t replace old wooden utensils, cutting boards, or other pans. The new they bought me pan was even carried home in a shopping bag with gluten bread in it, which triggered my OCD. It also has a rubber handle and I’m scared it might still hold onto gluten. Even if it’s washed well, it’s stored next to other pans that were used for gluten food/bread. Our kitchen table is used for eating gluten bread daily. My mom wipes it but not with soap. I’m scared tiny particles remain. If she made gluten-free bread dough on a board at the table, I’d still worry about cross contmaination contamination even with something under the dough and on the table as at one point the dough would probably touch the table. So I stopped eating anything she makes.   I know OCD is making it worse, but I can’t tell how much of my fear is real and how much is anxiety. Examples: • I wash my hands 20–30 times a day — before eating, after touching anything at home or outside, after using my phone/laptop. • I don’t let others touch my phone, and I’m scared to use my laptop because friends at school or my brother (who eat gluten) have touched it. And it annoys me a lot when others touch my stuff and feels like it got contaminated and is unsafe instantly. • I stopped eating while using my phone or laptop, afraid of invisible gluten being on them. • I wash my hands after opening food packaging (since it was on store cashier belts where gluten food is placed). • I avoid sitting anywhere except my bed or one clean chair. • I won’t shake hands with anyone or walk past people eating gluten. • At school, when switching classes, I wash my hands before getting out my laptop, again before opening it, etc. • I open door knobs with my elbows instead my hands   Job Concerns (Powder Coating, Sandblasting, Etc.) I’m working a temporary job right now that involves: • Powder coating • Sandblasting • Wet spray painting • Anodizing There’s also a laboratory. I don’t need this job, and my OCD makes me believe that dust or air particles there might contain gluten somehow. Should I quit?   Doctors Haven’t Helped My family doctor told me: “Asymptomatic celiac isn’t serious, if you have no symptoms, your intestines won’t get damaged, so you don’t need a gluten-free diet.” I knew that was wrong, but he wasn’t open to listening. I just nodded and didn‘t argue. My gastroenterologist (who’s also a dietitian) said: „If your antibodies are negative, there’s no damage. It might even be okay to try small amounts of gluten later if antibodies stay negative.“ Also said, pepper that says “may contain gluten” is fine if it only contains pepper. She was more informed than my family doctor but didn’t seem to fully understand celiac either.   Questions I Need Help With 1. Is it realistically safe to eat food my mom cooks, if we get separate pans/ and boards even if gluten is still used in the same kitchen? There will always be low risk of cc chances like that she will still touch stuff that was touched by her and my siblings after they ate gluten. And as there are gluten eaters in the house and she also prepares and eats gluten. So would opening the fridge then getting the food and touching the food be okay? So basically what i am doing, washing my hands multiple times while preparing food, she would only wash it once before, then touch anything else (for example water tap or handles) that were touched with gluteny hands, then also touch the food. I dont know if I ever could feel safe, I could try telling her how important cc really is. And I trust her so she wouldnt lie to me then be careless about cc, but idk how safe it really can be if she and everyone else keeps eating gluten and touching stuff in the house after eating. 2. Do I need to worry about touching doorknobs, fridge handles, light switches, etc. that family members touched after eating gluten? What about public places like bus handles or school desks? Or like if i went to the gym, I would be touching stuff all the time, so there will be small amounts of gluten and those would get transferred on my phone if I touch my phone while in the gym. But I want to knos if it would be enough to do damage. 3. Is an endoscopy (without biopsy) enough to tell if my intestines are healed? I’d pay privately if it could help and if i dont get a refferal. Or do i need a biopsy? 4. Could my job (powder coating, sandblasting, etc.) expose me to gluten or damage my intestines through air/dust? 5. Do I need certified gluten-free toothpaste, hand soap, shampoo, or moisturizer? (For example: Vaseline and Colgate don’t contain gluten ingredients but say they can’t guarantee it’s gluten-free.) 6. Is spices like pepper with “may contain traces of gluten” safe if no gluten ingredients are listed? Or does everything need to be labeled gluten-free?  7. Is continuing to only eat my own food the better choice, or could I eventually go back to eating what my mom cooks if she’s careful? 8. is cutlery from dishwasher safe if there are stains? Stuff like knives is used for cutting gluten bread or fork for noodles etc. I often see stains which i dont know if its gluten or something else but our dish washer doesnt seem to make it completely clean. 9. I wash my hands multiple times while preparing food. Do i need to do the same when touching my phone. Like if i touch the fridge handle, I wash my hands then touch the phone. I dont eat while using my phone but i leave it on my bed and pillow and my face could come in contact with where it was.  10. Do i need to clean my phone or laptop if theyve been used by people who eat gluten? Even if no crumbs fall onto my keybaord, i mean because of invisible gluten on their fingers. 11. Does medication/supplements have to be strictly glutenfree? One company said they couldn‘t guarantee if their probiotics don’t contain traces of gluten.  12. I had bought supplements in the past, some of them say glutenfree and some of them dont(like the brand „NOW“ from iherb). I bought them and used them when i wasnt washing my hands so often, are they still safe? As I touched and opened them after touching door knobs, water taps etc. It was like a year ago when i bought those and even though i was eating gluten-free, I never worried about what i touch etc. I know this post is long. I’m just extremely overwhelmed. I’m trying to protect myself from long-term health damage, but the OCD is destroying my quality of life, and I honestly don’t know what’s a reasonable level of caution anymore. Thanks for reading.
    • lmemsm
      I've been making a lot of black bean brownies lately because it's one of the few gluten free dessert recipes that actually tastes palatable.  I've also seen chocolate cake recipes with black beans.  Someone mentioned a cookie recipe using lentils in place of flour.  Just wondering if anyone's run across any tried and true recipes using beans, lentils or peas for desserts?  I've seen a lot of recipes for garbanzo flour but I'm allergic to garbanzo beans/chickpeas.  Was wondering if adzuki or pinto beans might be useful in replacing some or all of the flour in baking.  Since gluten free flours can be crumbly was hoping the beans might help produce a better, less crumbly consistency.  Any recommendations for recipes?  Thanks.
    • lmemsm
      I've seen a lot of recipes for chia pudding, so I decided to make some with chia, water, cocoa and honey.  Didn't like the taste, so I added ground sunflower and ground pumpkin seed to it.  It tasted okay, but came out more like frosting that pudding.  I used to make pudding with tapioca starch, milk powder, water and sugar.  It came out very good but I haven't figured out what to use to replace the milk powder to make it dairy free.  Most starches will work in place of tapioca starch but quantity varies depending on the type of starch.  If I didn't add enough starch to get a pudding consistency, I'd add gelatin as well to fix it.  Avocado and cocoa makes a good dessert with a pudding like consistency.  Unfortunately, I have a bad reaction to avocados.
    • lmemsm
      Seems like when I find a gluten free product I like, the producer stops manufacturing it and then I have trouble finding a new gluten free source for it.  What's worse, I've been contacting companies to ask if their products are gluten free and they don't even bother to respond.  So, it's making it very hard to find safe replacements.  I was buying teff flour at nuts.com and they no longer carry it.  I noticed Naturevibe has teff and soy flour.  However, I can't get a response as to whether their flours are safe for someone with celiac.  Can't get a response from Aldi if their peas are safe for someone with celiac either.  I know Bob's Red Mill has teff flour but was hoping to get a large quantity.  I've been using up the 20 ounce Bob's Red Mill teff flour too quickly.  Does anyone know of a good source for teff or soy flour?  Any recommendations where to get gluten free beans, peas or lentils?  I found some packages of gluten free beans at Sprouts but not much variety.  I've also been looking for lentil elbow macaroni and it seems like no one is making that now that Tolerant was bought out.  Any suggestions for safe sources for these types of ingredients.  Thanks.
    • chrish42
      All I can say is this site is great!
×
×
  • Create New...