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

Primal/paleo But No Nuts?


Celiac Mindwarp

Recommended Posts

Celiac Mindwarp Community Regular

Hi

I am loving the look of primal/paleo, and I know when I did Atkins years ago it was great.

However - my son has a severe nut allergy and we can't have them in the house.

I tried Atkins again recently, but struggled without nuts for snacks.

I can't have too much fruit, or any seseme either.

Can anyone suggest easy to carry snacks?

Many thanks


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



Celiac.com Sponsor (A8-M):



Adalaide Mentor

Due to an additional condition I was diagnosed with after celiac I am seed and nut free. I'm actually tyramine free but these are both included. Additionally I'm soy free so at first I spent the first few days convinced I would starve to death.

First, an easy and no sacrifice option. If it doesn't matter what you eat you could keep Kind bars or Larabars in your desk at work and just be sure you practice handwashing and if necessary brush your teeth or whatever before you leave. Not sure if that's an option for you but you'd be able to have nuts, it's a quick and great snack and they'd never be in the house.

There isn't much in the way of grab and go snacks I can have anymore but I do keep fruit snacks or fruit leather handy. Costco usually has huge boxes of super awesome fruit leather for a reasonable price. My husband prefers fruit snacks and they are cheaper so it's what we more commonly have on hand. We keep fresh vegetables washed and ready to snack on available 100% of the time. Again, Costco to the rescue, I can get a 5 pound bag of organic, washed and ready to eat baby carrots for $5. I throw together some yogurt tiziki dipping sauce to keep on hand also. Instead of fatty sour cream we're shoveling probiotics and cucumbers in our face with our veggies. I also like to keep large (huge) containers of grape tomoatoes, the yellow ones. Nature's candy.

Popcorn can be healthy. It isn't the way I like it but in theory it's a great healthy snack. If you aren't dairy free I am a huge fan if Laughing Cow cheese wedges with rice crackers. You wouldn't be able to buy the huge huge boxes of Crunchmaster at Costco because half are sesame (unless you can pawn those off on the other half of the house) but half are parmesan, both are delicious. Really, any good cracker or whatever. Or just the cheese! Or string cheese with fruit. I know you said not too much fruit but you could split an apple with your son and have some sliced cheddar or string cheese. Always a favorite here. I also do a lot of cottage cheese and fruit, heavy on the dairy light on the fruit for you I suppose. Actually, I usually just make that a meal and add flax.

Anywho, that's just some ideas of what we do around here. I keep steering my husband more and more away from his fatty diet to more and more healthy stuff. He says I'm turning him into a hippie. :lol:

Celiac Mindwarp Community Regular

That's great, thanks

I feel a bit like I'm living on cheese some days! Fingers crossed I dont turn out intolerant...

I need to be a bit more prepared I think.

Hippie is good, in my view. I have yet to convince my family about better eating. Though my husband did say he was jealous of my breakfast of rice avocado chicken and gluten-free soy sauce. Maybe eventually...

Celiac Mindwarp Community Regular

I know, I've not started the diet yet!!!

LauraB0927 Apprentice

I'm on the primal diet, go to work 9-5, and then school from 6-10pm. So I've been trying to live on primal snacks since I dont trust my school's cafeteria and obviously cant cook a steak in my classroom. Besides nuts, I always carry around with me some unsalted sunflower seeds, gluten free beef jerky, cheese, yogurt (I know its not primal, but a girl's gotta eat!), carrots, and they sell little snack packs of the dried cranberries (Craisins) that really come in handy. It definitely holds me over until I get home! Best of luck!

Celiac Mindwarp Community Regular

Wow, I remember when I used to have energy like that, well done for sticking at school.

Some great ideas, thanks, I'd forgotten about sunflower seeds, I really like those

Thanks

LauraB0927 Apprentice

Wow, I remember when I used to have energy like that, well done for sticking at school.

Some great ideas, thanks, I'd forgotten about sunflower seeds, I really like those

Thanks

Hahaha who said I had energy???? :) But thanks!!


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,862
    • Most Online (within 30 mins)
      7,748

    Aracely
    Newest Member
    Aracely
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.5k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Villi damage is caused by celiac disease, which does not happen in NCGS, although some people with NCGS do have elevated antibody levels. Some people with NCGS who have the genes for celiac disease may end up developing celiac disease, so in some people NCGS may be a precursor to celiac disease, but more research needs to be done on NCGS. Both low iron and vitamin D are common symptoms of celiac disease. Also, regarding beer:  
    • Scott Adams
      It’s true that some vaccines contain small amounts of preservatives, stabilizers, or adjuvants to ensure their safety and effectiveness. For example: Thimerosal: A preservative that contains ethylmercury (not to be confused with methylmercury, which is toxic). Most routine vaccines no longer contain thimerosal, except for some flu vaccines in multi-dose vials. Aluminum: Used in very small amounts as an adjuvant to boost the immune response. The amount is far below levels considered harmful, but if you suspect an aluminum allergy, it’s worth discussing with your doctor. Sugar alcohols: These are sometimes used as stabilizers, but they are generally well-tolerated. If you have a known intolerance, you can ask about specific ingredients in each vaccine. Since you mentioned an intolerance to metals and jewelry, it’s a good idea to follow up with allergy testing, as you planned. This can help identify specific metals (e.g., nickel, aluminum) to avoid. Your doctor can then guide you on whether any vaccine ingredients might be a concern. Since the Mayo Clinic has already identified potential allergies, it might be helpful to consult an allergist or immunologist. They can review your medical history, perform tests, and provide personalized advice on vaccines and their ingredients. While it’s important to address your intolerances, it’s also worth considering the risks of not being vaccinated. Many vaccine-preventable diseases can have serious consequences, especially for those with underlying health conditions. 
    • knitty kitty
      @Manaan2, I was on Miralax for several months after I crushed three vertebrae and fractured my hip.  The compression fractures of my vertebrae affected the Vagus nerve that stimulates digestion and intestinal movement, peristalsis. Miralax just didn't relieve the constipation I was experiencing at all.  Nothing budged.  I tried Milk of Magnesia (magnesium oxide) which pulls water into the digestive tract, and found that rather harsh and dehydrating.   Bad idea. I was already taking thiamine in various forms, Benfotiamine, TTFD (tetrahydrofurfuryl  disulfude), Lipothiamine and Allithiamine.  Click on my name, then Activities in the pull down menu to get to my blog to learn more about my journey with thiamine.   Since we need more thiamine when we are physically ill and emotionally stressed, I decided to focus on TTFD,  Benfotiamine, and magnesium l-threonate.  Within a week of increasing my doses a bit, my constipation was gone.  It took several more months to heal the compressed nerve damage.  For pain, I take a combination of TTFD, Pyridoxine B 6, and  Cobalamine B12 which together have an analgesic effect.  I can't function with pharmaceutical pain killers, besides they cause constipation.   Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Yes, I did just stop the Miralax, but I wasn't on it as long as your daughter.  Yes, there's a difference between adults and children.  Yes, my circumstances were different than your daughter's, but thiamine deficiency does affect the nerves and the brain.  A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function (which activates the Vagus nerve and controls digestion).   I recommend you visit Dr. Chandler Marrs' website, hormonesmatter.com.  Dr. Marrs worked with Dr. Derrick Longsdale, a pioneer in thiamine research, specifically with children and autism spectrum disorders.  She has been very helpful to me when I reached out to her.  She would be better able to guide you about your daughter's care. https://hormonesmatter.com/sibo-ibs-constipation-thiamine-deficiency/#google_vignette Do stay in touch, please.  You can start another thread or personal message me any time.  My heart goes out to you, your husband, and especially your daughter.   Namaste
    • Manaan2
      @knitty kitty  The information you've provided is invaluable!  I have a lot more homework to do before we make the official switch but you have significantly increased my hope that we can get her off Miralax (she started at 3 years old and is almost 8!).  This weekend my husband and I plan to solidify all the details for a start point, then adjust as we go along.  I realize that everyone's body is different, then there's also the fact that she's a child but just out of curiosity if you don't mind sharing and if you'd rather not, no problem at all-how long did you take Miralax before switching and when you switched, did you just completely stop the Miralax or was there a period where you did Miralax and the supplements?  I plan to research that piece this weekend but just curious what you did.  
    • BIg Nodge
      Scott, thanks so much for the thoughtful replies. My doctor did actually just re-order thyroid labs to see what is going on with my TPOs. I agree that will be interesting information.  I think I know the answer to this, but as far as the biopsy . . .. that would be quite conclusive as far as celiac goes, but a negative result would not rule out NCGS, correct? Does NCGS also cause damage to the lower intestine/leaky gut?  I appreciate the thought that I should be open-minded to other causes. I did not have dysautonomia on my radar, so I will look into that. From a quick scan at the potential symptoms it seems like almost anyone could convince themselves they have it, very broad! I can see why that is a tricky one to diagnose. I did also show low vitamin D, I'm in New England so that is somewhat common. I have a memory of low iron on some lab result as well but I can't find it, so I'll look into that. My cholesterol is high too, so working on that.  While the initial adjustment was tough, I have actually adapted fairly well to going gluten-free at home. The tough part for me is I love eating out and traveling, so that has been a challenge. I suppose if the answer ends up being NCGS then I could maintain a mostly gluten-free diet but also experiment with the occasional splurges. Snowboarding just doesn't feel right without a beer in the lodge . . ... cider is just not the same!  Thanks again.  
×
×
  • Create New...