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

Need Some Variety


Dru

Recommended Posts

Dru Rookie

Hey all,

I have finished my elimination diet and am now avoiding:

Gluten, Dairy, Soy, Corn, Yeast, Coconut, Peanuts, Egg Yolk (whites are okay).

I do not eat red meat or pork but can sub ground chicken for ground beef recipes. I should also mention that the only nuts I eat are cashews and I can not eat raisins or citrus fruit but all other fruit is fine.

I am trying to find some things that I can make for dinner. I usually take whatever I eat for dinner as leftovers for lunch the next day. I am also supposed to be working on increasing the amount of vegetables that I consume.

I have just bought a crock pot and would be interested in some recipes for that.

I am also looking for a way to make chocolate chip cookies (and other baked goods) without margerine or butter since there is not one that is dairy/soy/corn free. I can use Spectrum shortening or several types of oil but I don't know how to convert recipes that call for margerine or butter.

Also, any suggestions for snack foods that I can easily take to work or eat in the car would be great (I commute 2 hours each way twice a week).

I appreciate any advice or tips you can give. I hope I don't sound whiny. I know that there is a lot of food out there that I can still eat but I was not a cook before this new diet and am not used to any of this (especially the gluten free flour thing). Basically, I have been eating rice, fish, plain chicken, and homemade turkey and bean chili for a month now and am getting sick of it.


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



Celiac.com Sponsor (A8-M):



Juliebove Rising Star

I buy some pumpkin seed bars from Goraw that should be safe for you to eat. I also eat raw pumpkin seeds. I like them better than the roasted ones. Daughter eats turkey sticks that should be safe for you. They're made by Shelton's. You could also eat raw veggies but you'd have to keep them in a cooler to make sure they stay fresh.

We had tuna casserole last night. I made the sauce out of a couple of handfuls of mushrooms, a couple of ribs of celery and a big handful of onion, all chopped. I cooked them in olive oil until soft, then added some sweet rice flour and water. Seasoned with salt, pepper and parsley. To this I added 3 packs of tuna, and a small package of quinoa pasta. You can use rice pasta, but I prefer the quinoa. Also added a can of peas. I usually use frozen peas but I was out of them. Bake until heated through and top with some potato chips. I put the chips on each serving because they get soft on the leftovers.

You can try varying the types of rice you are eating. We like wild rice on occasion.

For the crockpot, you could try a chicken stew. Cut some chicken into bite sized pieces. Brown it first in a skillet with a bit of oil. Add to it whatever vegetables you like. Use fresh or raw, cut up if necessary. I'd use carrots, potatoes, peas and green beans. You can also use canned but you'd need to add those almost at serving time because they are already cooked. Season with salt, pepper, parsley and perhaps a bit of poultry seasoning. Add some chicken broth and if you like, thicken it with sweet rice flour or mashed potato flakes. Very nice dish for winter.

We've recently bought rice based yogurt and cheese. We like the cheese on pizza and nachos. For the pizza, I use Ener-G rice crusts. Top with your favorite tomato sauce. I use lots of vegetables on mine. Daughter likes meat. Bake as directed. Then add the rice cheese and bake until the cheese is melted. Just be sure to buy the Vegan cheese because it has no dairy in it. This pizza is also good with just the tomato sauce and cheese.

For the nachos, start with a pile of chips. You'd have to use rice chips. Top with little blobs of canned refried beans and pieces of rice cheese. Nuke until the cheese melts, then sprinkle on chopped tomato, green onion, black olives and serve with salsa. You can also add cooked meat to this if you want. Very good!

You can also make a dip of canned refried beans and rice cheese and serve it with chips or raw veggies.

confusedks Enthusiast

Juliebove,

What brand of cheese do you use? Is it soy free?

Kassandra

Dru Rookie

Wow, thanks for all those great ideas. I guess I'm just not very creative yet. Being a mom to a toddler and a full time student I had been "cooking" by adding whatever the box/mix told me to and heating it up. That doesn't work anymore.

I too am interested in the brand name of the cheese. I haven't been vegan since the mid-90s and I'm sure that there is more out there now but I seem to recall all of the rice cheese having either casein or soy in them. I used to be able to eat soy so this was not a problem back then.

Thanks again for all the great ideas.

moonlitemama Rookie

I believe the cheese brand is Galaxy International. One of their cheeses is gluten-, soy-, and dairy-free. I haven't been able to get it locally, though, so I haven't tried it.

Ricera yogurt is also gluten-free, SF, DF and might work for you (not certain of the other ingredients, so you'd want to double-check). I don't care for it plain, but find that it's great for a smoothie. I use frozen strawberries, a little sugar or agave nectar, water and a container of strawberry or vanilla yogurt. It also works great for a coffee cake recipe I've created. Let me know if you're interested.

For snacks on the go, I like Lara bars (I think there are some that use only cashews as the nuts). Also, trail mix - you could use cashews, pumpkin seeds, sunflower seeds, dry fruits, cereal (maybe something like Arrowhead Mills Organic Maple Buckwheat Flakes).

For baking, I haven't tried many recipes yet, but I think for cookies you can just substitute straight across Spectrum Shortening for the butter/margarine. I'll be interested if anyone can share how to sub oil for the butter/margarine.

You might look at Road's End Organics boxed pastas. I think they may meet your requirements. I like the penne pasta w/ cheese, but didn't care for the macaroni one. Something easy if you're used to cooking from a box.

I'm gluten-, casien-, soy- and glutamate-free and it's definately a tricky combination. Good luck. It will get easier!

sparkles Contributor

you might take a look at Cherrybrook chocolate chip cookie mix. I found some at a super Target. It wasn't bad.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,979
    • Most Online (within 30 mins)
      7,748

    volivier
    Newest Member
    volivier
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      @Riley, on this forum we sometimes get reports from people with similar experiences as you. That is, their celiac disease seems to go into remission. Typically, that doesn't last. At age 18 you are at your physical-biological peek in life where your body is stronger than it will ever be and it is able to fight well against many threats and abuses. As Wheatwacked pointed out, absence of symptoms is not always a reliable indicator that no damage is being done to the body. I was one of those "silent" celiacs with no symptoms, or at least very minor symptoms, whose body was being slowly damaged for many years before the damage became pronounced enough to warrant investigation, leading to a diagnosis. By that time I had suffered significant bone demineralization and now I suffer with back and neck problems. Please, if you choose to continue consuming gluten, which I do not recommend, at least get tested regularly so that you won't get caught in the silent celiac trap down the road like I did. You really do not outgrow celiac disease. It is baked into the genes. Once the genes get triggered, as far as we know, they are turned on for good. Social rejection is something most celiacs struggle with. Being compliant with the gluten free diet places restrictions on what we can eat and where we can eat. Our friends usually try to work with us at first but then it gets to be a drag and we begin to get left out. We often lose some friends in the process but we also find out who really are our true friends. I think the hardest hits come at those times when friends spontaneously say, "Hey, let's go get some burgers and fries" and you know you can't safely do that. One way to cope in these situations is to have some ready made gluten-free meals packed in the fridge that you can take with you on the spot and still join them but eat safely. Most "real" friends will get used to this and so will you. Perhaps this little video will be helpful to you.  
    • Wheatwacked
      @Riley., Welcome to the forum.   It was once believed that Celiac Disease was only a childhood disease and it can be outgrown.  That was before 1951, before gluten was discovered to be cause of Celiac Disease, also called Infantilism.  Back then Cileac Disease was thought to be only a gastro intestinal disease, once you  "outgrew" the colicky phase, you were cured. You were so lucky to be diagnosed at 5 years old so your developing years were normal.  Gluten can affect multiple systems.  The nervous system, your intellegence. The muscules, skeleton. It can cause neurological issues like brain fog, anxiety, and peripheral neuropathy.  It can cause joint pain, muscle weakness, and skin rashes. Epilepsy is 1.8 times more prevalent in patients with celiac disease, compared to the general population. Because through malabsorption and food avoidances, it causes vitamin D and numerouus other essential nutrient deficiencies, it allows allergies, infections, poor growth, stuffy sinuses and eustacian tubes. There is even a catagory of celiac disease called "Silent Celiac".  Any symptoms are explained away as this, that or the other thing. Gluten is one of the most addictive substances we consume.  Activating the Opiod receptors in our cells, it can numb us to the damage that it, and other foods are causing.  It has become socially acceptable to eat foods that make us feel sick.  "There's a pill for that".   It is generally accepted that n fact you are weird if you don't. The hardest part is that if you don't eat gluten you will feel great and think why not.  But slowly it will effect you, you'll be diagnosed with real diseases that you don't have. You'll be more susseptable to other autoimmune diseases.  As you read through the posts here, notice how many are finally dianosed, after years of suffering at older ages.  Is it worth it? I think not. Perhaps this book will help:  Here is a list of possible symptoms:   
    • Riley.
      Hi! Im Riley, 18 years old and have been diagnosed for 13 years.. the testing started bc I stopped growing and didn’t gain any weight and was really small and thin for my age.  I got diagnosed when I was 5 and have been living gluten free since, in elementary and middle school it was hard for me and I kept contaminating myself bc I wanted to fit in with my friends so so badly. I ate gluten secretly at school and mostly regretted it 30 minutes later.  I’ve had symptoms like diarrhea, nausea, headaches, stomachaches, threw up a lot and was really emotional.  In 2022 I really started working on myself and tried to stay gluten free and if I did eat gluten I wouldn’t tell anyone and suffer in silence.  Last year in July I begged my mom to let me „cheat“ one day bc I just wanted to fit in… I ate a lot of different stuff, all the stuff I missed out on in my childhood like nuggets, pizza and all that.. I didn’t have symptoms that day and was doing really fine My mom and I wanted to test how far we can go and said we would test it for 12 weeks to get my blood taken after to see if I’m doing good or if symptoms start showing  As a now 18 year old girl who finally gained a normal weight and doesn’t get symptoms I’m to scared to get tested/my blood taken cuz I finally found comfort in food and it got so much easier for me and my family.  A year and 4 months later i still didn’t get any symptoms and have been eating gluten daily.  I’m scared to get tested/my blood taken cuz what if I’m actually not fine and have to go back to eating gluten free. Any tips to get over that fear and „suck it up“ cuz I know I could seriously damage my body… sorry if I seem like a idiot here… just don’t really know what to do :,)
    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
×
×
  • 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.