Jump to content
  • 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

Gluten Free Nuts & Seeds


Mama Melissa

Recommended Posts

Mama Melissa Enthusiast

Hello All,

I am having a hard time finding nuts and seeds that are gluten free??Does anyone know any mainstream brand nuts or seeds that are gluten free??I really want some to throw in my salads and just to munch on in general:)I have looked at planters products alot of them say conains wheat. Why in the world would you put wheat in nuts???UGh they should ban wheat all together that evil evil grain lolz..


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



Celiac.com Sponsor (A8-M):



cap6 Enthusiast

Check out Planters Dry Roasted Peanuts. The only listed ingredient is peanuts. I eat them a lot. I agree - what's with wheat products in nuts???

fakename Contributor

Hello All,

I am having a hard time finding nuts and seeds that are gluten free??Does anyone know any mainstream brand nuts or seeds that are gluten free??I really want some to throw in my salads and just to munch on in general:)I have looked at planters products alot of them say conains wheat. Why in the world would you put wheat in nuts???UGh they should ban wheat all together that evil evil grain lolz..

I'm a major nut eater and I always eat planters -at least most of their peanut, mixed nuts, and cashew brands do not contain wheat.

But I heard from them about a year ago that they don't know about if their facilities are gluten free they just know that they'll tell you if they are free of the "common allergens".

Nuts Online have gluten free raw cashews and other products -but they cost like $20/ibs.

BethM55 Enthusiast

I buy most of our nuts and seeds at Trader Joe's. The ingredients on the bag of dry roasted and unsalted almonds is..... Almonds. I've never had a problem eating these or the cashews, or the sunflower seeds. I've bought the pepitas (pumpkin seeds) too. Simpler is better, I think.

Mama Melissa Enthusiast

Thank you for your input:)Beth i agree i bought pistachios from target which ingridients just said pistachios.Well that night well over half of the contsainge ri had the runs all day the next day it was HORRIBLE.I am not terribly sensitive like some others and i am not sure if it was just because i ate to many or a gluten reaction it seemed to be more of a reaction i eat nut bars and peanuts in shell all the time without reactions so this left me confused:(

Racer-J Newbie

I'm a major nut eater and I always eat planters -at least most of their peanut, mixed nuts, and cashew brands do not contain wheat.

But I heard from them about a year ago that they don't know about if their facilities are gluten free they just know that they'll tell you if they are free of the "common allergens".

Nuts Online have gluten free raw cashews and other products -but they cost like $20/ibs.

Nutsonline has them for $10.99 a lb (raw/organic) & $7.99 a lb (raw/organic/pieces). They also have conventional raw cashews that are slightly cheaper. However, with the cost of shipping & handling, it does approach the $20.00 a lb price so, I guess that's what you were referring to. If you ignore the cost of shipping, the price of cashews is almost identical to what Whole Foods charges in the bulk bins. Some of the prices of other items at Nutsonline are the same as Whole Foods bulk bins and, some of them are more expensive. The shipping & handling is really only "expensive" if you order 1 lb at a time. Since the OP was looking for multiple types of nuts and seeds, the shipping & handling may not increase the cost of each item much. For example, if I were to buy 6 lbs total, the shipping would be $10.40 total. Broken down, that would add $1.73 to each lb which is probably about the average markup for a certified gluten-free item vs a non certified one. The shipping & handling cost can be offset if you order enough compared to just ordering 1 lb. It will probably never zero out though as 12 lbs shipped to me would be $12.50 total. Broken down that would be $1.04 a lb. It's really a question of if total weight of all the items you order is going to be reasonable compared to the added cost from shipping & handling.

A quick note on "raw" cashews though. From what I have read, there are two ways "raw" cashews are shelled. One is by steaming which technically doesn't make them "raw". The other way is by a mechanical device that actually removes the shell. The mechanical advantage is that it keeps them "raw" in case that is a deal breaker. The steaming advantage is that it makes the nut nontoxic. There is actually a toxin in the shell and since the steam doesn't really make physical contact, the toxin can not get onto the nut. However, there is a chance the toxin can transfer from the mechanical device to the nut since there is physical contact.

The point is, it is entirely possible to get sick from eating "raw" cashews that were shelled mechanically so, take caution if that happens and don't be quick to blame it on CC. The typical advice I have seen is it's pretty rare to get sick from the toxin if you eat less than a 1/4 cup of them a day. Again, this only applies to "raw" cashews shelled mechanically. I'm not sure how the ones from Nutsonline are shelled. However, they do say they are not pasteurized and the only way nuts are pasteurized is via steam or a chemical. The chemical is not allowed for use in organic food which leads me to believe the "raw" cashews they sell are probably shelled mechanically.

"raw" cashews also have a vastly different taste and texture than roasted ones so take that into consideration if you have never had them. Vegan recipes for nut based cheeses/creams/etc. containing cashews usually specify them to be "raw". Having eaten them, I can see why. They are extremely "creamy" when you chew them compared to roasted ones and the flavor is more subtle and "smooth". I honestly prefer the taste of roasted but, both have their time and place.

Thank you for your input:)Beth i agree i bought pistachios from target which ingridients just said pistachios.Well that night well over half of the contsainge ri had the runs all day the next day it was HORRIBLE.I am not terribly sensitive like some others and i am not sure if it was just because i ate to many or a gluten reaction it seemed to be more of a reaction i eat nut bars and peanuts in shell all the time without reactions so this left me confused:(

Pistachios are generally considered to have a high mold content just like peanuts. From what I gather, it really only applies to their shelled incarnations. Unshelled pistachios and peanuts have substantially less mold but, they are still higher in mold content than any other nut or seed. It also could have been CC as several different products are sold under the "Applegate Farms" Target brand. It's just like any other "store label" brand. It's just an "unbranded" name brand. An "article" on Livstrong says that diarrhea is not a common allergy symptom for pistachios but, it probably isn't taking into a account a compromised digestive system and anyone can write an "article" online. There was also a major recall of pistachios in 2009 due to salmonella CC.

I hate this disease. It makes it incredibly difficult to figure out what and why.

Having said all of that, I know this was an odd first post for me lol. I just felt compelled to post on this topic.

I don't have an official diagnosis. My father is a diagnosed Celiac though and my aunt and her daughter were negative to the Celiac blood test but, came up positive for gluten sensitivity on the EnteroLab $99 test. My aunt had a score of 40 and her daughter had a score of 13. Given all of this and all the food sensitivities/intolerances/allergies I have developed within the past few months after being gluten free for 6 months (ignoring the inevitable CC & random glutening), I'm pretty sure I have issues with it as well. I wasn't working at that time and the blood test was just to expensive. I made the analytical decision to just drop it from my diet and have never looked back nor had any cravings for any gluten product. I am currently in the process of collecting a sample for the EnteroLab $99 test though. Apparently it can still detect issues with gluten up to a year after you stop ingesting it. The blood test will never be an option for me as I absolutely refuse to knowingly ingest gluten and that simply will not ever change. I have just seen to much change and, discovered to many other issues since I stopped ingesting it to ever submit my body to that type of chaos again. If an official diagnosis would make all the gluten stuff free, then I might consider taking it lol.

For even further disclosure, I have never used Nutsonline. I will be ordering hazelnuts and sunflower seeds from Nutsonline next month to see how that goes. I just no longer trust the bulk bins at Whole Foods given the problems I tend to have after eating something from them. I need to rule out the bloating from being a CC issue or an issue with the actual food in question. That really helps me to justify the cost of shipping even if I am just going to be ordering 2 lbs a month.

BTW, when I say bloating, I mean gaining 5-6 inches in my entire abdomen within 5 - 10 minutes of eating 2 teaspoons. It is ridiculous. It even happens when I eat the certified oats from BRM (Bob's Red Mill) or the Organic Brown Basmati Rice from Lundberg Farms. To be fair, that could be an issue with oats considering Lundberg Farms uses them as a cover crop. However, given I have similar issues with all the other gluten free grains and corn, I have removed any and all grains from my diet. That got rid of my miscellaneous aches & pain and the delicious taste of rice and oats isn't worth getting it back. I do really miss Mexican food though but it is severely lacking once you have to ditch onions, peppers, beans, corn, and flour tortillas (because corn tortillas are gross lol) for various reasons. WARNING (TMI ALERT): The onions and peppers don't cause bloating but they feel like lava coming out.

Sorry for getting off topic but, I wanted to be thorough about why I posted and why I joined. Especially since this post has to be approved my a mod :P

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to tiffanygosci's topic in Introduce Yourself / Share Stuff
      2

      Celiac support is hard to find

    2. - cristiana replied to Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      Newly diagnosed mam to coeliac 11 year old

    3. - tiffanygosci replied to tiffanygosci's topic in Introduce Yourself / Share Stuff
      2

      Celiac support is hard to find

    4. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    5. - mamaof7 posted a topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,958
    • Most Online (within 30 mins)
      7,748

    DLA
    Newest Member
    DLA
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • cristiana
      Hi @tiffanygosci Well done for reaching out,  fantastic you have found this forum. It sounds like you are managing the diet well, it can be overwhelming at first, but it will get easier.     I wonder if you have seen the short film 'Glutened'? - someone shared it on this forum a few months ago and it reminded me of how isolating it can be, particularly at first, when you don't know anyone with celiac disease.  *see link for film below. I realise now how blessed I was that when I was diagnosed two friends were also diagnosed around the same time, as we shared a lot of tips and recipes at the start.   Since then the number of people I know diagnosed with coeliac disease has grown and grown, there seems to be a much greater awareness of it among healthcare professionals and the public, at least this side of the Atlantic (I'm British).  I think in time you may find this, too. That said, those two coeliac buddies were 'straightforward' cases who seemed to recover very quickly when on a gluten-free diet - I struggled for some time.  So I found that I spent much more time discussing things with this online coeliac family. If you have any more questions, we're here for you.  I hope your event on 15th goes well.  Sounds like a good start!  I like you am not keen on Facebook, but perhaps setting up an account short-term might help? * https://vimeo.com/486284734 Cristiana     
    • cristiana
      You are very welcome @Dizzyma. Gastroenterologists are now following this rule in the UK more and more with children, so I am not surprised your daughter is not having an endoscopy.   Switching to a gluten free diet should begin to help, but also, even if you have to have testing done privately, it would be very helpful for you to find out if your daughter has vitamin and mineral deficiencies, which is highly likely,    In the UK tests are generally offered on the NHS for B12 and ferritin, and sometimes vitamin D.  Shortages in these can really cause any anxiety or depression or ramp it up. If you do end up supplementing, make sure your GP is aware as levels do need to be monitored, for example,  too much ferritin can cause huge health issues. Re: anxiety, definitely speak to a GP or another health care professional about this if it is an issue. Hopefully the Coeliac Society of Ireland will also be able to help. Cristiana  
    • tiffanygosci
      EDIT: I did find a monthly Zoom meeting for Celiacs through the Celiac Disease Foundation, so I'll be able to talk with some other people on January 15. And I also found a Celiac Living podcast on Spotify made by a celiac. I feel a little bit better now and I am still hoping I will find some more personal connections in my area.
    • trents
      Welcome to the celiac.com community, @mamaof7! It means for the one celiac disease antibody test that was ordered, she tested negative. However, other tests should have been ordered, especially for someone so young who would have an immature immune system where there would be a high probability of being IGA deficient.  The one test that was ordered was an IGA-based antibody test. It is not the only IGA antibody test for celiac disease that can be run. The most common one ordered by physicians is the TTG-IGA. Whenever IGA antibody tests are ordered, a "total IGA" test should be included to check for IGA deficiency. In the case of IGA deficiency, all other IGA tests results will be inaccurate. There is another category of celiac disease antibody tests that can be used in the case of IGA deficiency. They are known as IGG tests. I will attach an article that gives an overview of celiac disease antibody tests. All this to say, I would not trust the results of the testing you have had done and I would not rule out your daughter having celiac disease. I would seek further testing at some point but it would require your daughter to have been eating normal amounts of gluten for weeks/months in order for the testing to be valid. It is also possible she does not have celiac disease (aka, "gluten intolerance") but that she has NCGS (Non Celiac Gluten Sensitivity, or just "gluten sensitivity" for short) which is more common. The difference is that celiac disease is an autoimmune disorder that damages the lining of the small bowel whereas NCGS does not autoimmune in nature and does not damage the lining of the small bowel, though the two conditions share many of the same symptoms. We have testing to diagnose celiac disease but there are no tests for NCGS. To arrive at a diagnosis of NCGS, celiac disease must first be ruled out. A gluten free diet is the solution to both maladies.   
    • mamaof7
      For reference, daughter is 18 mths old. Was having painful severe constipation with pale stool and blood also bloating (tight extended belly.) Liver and gallbladder are normal. Ultrasound was normal. Dr ordered celiac blood test. We took her off gluten after blood draw. She is sleeping better, no longer bloated and stools are still off color but not painful.    "GLIADIN (DEAMID) AB, IGA FLU Value  0.84 Reference Range: 0.00-4.99 No further celiac disease serology testing to be performed. INTERPRETIVE INFORMATION: Deamidated Gliadin Peptide (DGP) Ab, IgA A positive deamidated gliadin (DGP) IgA antibody result is associated with celiac disease but is not to be used as an initial screening test due to its low specificity and only occasional positivity in celiac disease patients who are negative for tissue transglutaminase (tTG) IgA antibody."   Anyone know what in the world this means. She isn't scheduled to see GI until late April. 
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.