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

The Financial Aspect


au natural

Recommended Posts

buffettbride Enthusiast

We went through a phase when my daughter was first diagnosed of trying every gluten-free replacement product on the market. Most of them tasted so icky at first because that isn't what we were used to. We went primarily on a whole-foods diet. Many fresh veggies, but often frozen to save money as well.

Now we have a few packaged gluten-free foods that are staples...some cereal, rice bars, rice bread, pamelas mix, etc. but 90% of what we buy at the store is either naturally gluten-free or from a company we trust. We'll try a new gluten-free product every few weeks or so just to see if we stumble along any gems.

One way we save money now is with meats. We buy the "family pack" which usually results in 2 meals for our family of four. We divide the meat when we get home from the store. If it's just you or you and one other person then you could probably stretch that even further. That works really well for chicken breasts and pork chops especially.

We have also taken to making our own cripsy chicken strips. We get the chicken strips raw from the store then make them ourselves at home and freeze them. Those are a super handy dinner for the nights I don't want to cook.

Our biggest shocker wasn't so much the price, but the lack of convenience with gluten free foods. Making a lot of food then freezing half of it for a later meal has really helped out.

We keep a few cans of Progresso Veg/Rice soup on hand always too, in case we're in a real pinch.

It really does get easier, and less expensive. We probably spend more $ on groceries than most (almost $800 per month :o ) but my husband and son (who is only 3) are big eaters.


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



Celiac.com Sponsor (A8-M):



confusedks Enthusiast

It is difficult because we are shopping about every 3 days. We are lucky to have a Trader Joe's almost walking distance and multiple Whole Foods fairly close. We don't even really go to Ralphs, Vons, etc. anymore. Also, we have gotten smart about things. We used to but frozen rice all the time and just heat it up, but if we just make one big batch and put it in containers and heat it up as we go, it works great it is WAY cheaper! We use the crock pot a lot too. Our favorite meal is take two cans of salsa and whole chicken but up (buy for about $5) and put it in the crock pot for 4-5 hours on high. It is SO good. We put it over brown rice. It costs about $10 but lasts us for days. Its totally worth it. Another great cheap meal is talapia. Trader Joe's sells it for about $3 for 3 fillets. That is SO cheap! We just put olive oil, lemon and seasonings and put it in the broiler and it's so good.

It was much more expensive when I first went gluten-free, but we don't but really expensive gluten-free treats anymore. It will get easier. But in bulk, and package stuff individually when you get home.

Kassandra

kbtoyssni Contributor
I have also read some where that the difference between the cost of our foods vs normal diets can be deducted on your tax return. It doesn't help much now, but maybe it will at the end of the year. I haven't actually checked into it but I did read it some where on here.

The tricky part is this amount has to be more than 7% (or is it 12% - can't quite remember) to take a medical deduction. For most people, it would be hard to spend this much.

I do all my shopping at the regular grocery store, not a gluten-free specialty store, which really keeps costs down. I buy in bulk and shop the sale rack. I have also found rice flour for $2 for four pounds in the asian section of my store. The "ethnic" foods are much cheaper than buying the ones that say gluten-free on the package.

Centa Newbie

Welcome to the site, au natural

$5.00 to $8.00 dollars for a measly 24 ounces of soy, garbonzo and other flours is mindboggeling. I understand companies making money off gluten-free products... but the prices I am forced to pay to just eat.. feels like others are making money off my disability. I am forced to pay or just not eat. I thought why not just buy for example"garbonzo beans" and grind them myself?? The result was I would have to shill out $200-$300 bucks just for the grinder and then the shelf life of the flour is so low that it would be a waste to grind a pound at a time. How do you guys deal with this issue???

Asian markets do have rice flour. They also sell considerably more inexpensive garbanzo flour than what you're buying in health food stores. Look for the name "gram flour" It's also called "besan flour." Asian markets are a great place for buying lentils and other legumes, too. Oh, and bags of rice, and if you're into that kind of thing, you can buy the spices in inexpensive packets, get a $10 coffee grinder and grind your own spices.

Good luck with it, though au natural. Those gluten free items in health food stores have killer price tags often.

CtheCeliac Rookie

I'm sure your extra limitations make the the gluten-free diet even more challenging. I've been on the gluten-free diet 11 months. At first, the costs were overwhelming to me, (especially when despite my poor health and positive bloodwork, my doctor said if the biopsy was positive the diet would be expensive). Hey, I'm saving money by not buying so much Immodium AD :( and maybe on other future medical costs, such as possible osteoperosis or other problems.

Now I'm finally finding some ways to cut food expenses, but, like you, :) still struggle with the costs of some items. I've cut back on how many specialty foods I buy from the health store. A recent favorite is making my own chicken broth and adding leftover shredded chicken; navy beans; a few tablespoons of gluten-free flour; cumin; finely chopped carrots, peppers, and onion; diced green chilies; and rice for soup. Top with crushed tortilla chips. Soups are usually fairly cost-effective. (I saw a recipe today for soup with tomatoes, cabbage, juice, onions, and salsa.) Anybody tried to freeze soups you've made? :huh:

I also starting gardening again this year. The cooked gluten-free breakfast foods go a long ways for the cost. My brother and I have looked for gluten-free food specials and buy in bulk, then split costs. He joined a co-op at a health food store where he can get discounts certain times of the month. My best savings :) have been from going to a bent-n-dent store or overstock store (watch too many dents and expiration dates).

little d Enthusiast

At first I found it very hard to buy a loaf of bread that was $4.99 - $5.99 which is the most expensive item that I buy that is gluten free. I do buy a lot of food from walmart the value brand which are priced ok.

My shopping list at Whole Foods include which I can not find at regular stores

Bread (My Kroger does carry Kinninnick breads so I do go there at times)

Brown rice tortillas (I can not stand regular Corn tortillas)

Amy's rice pizza crust

Sunshine patties

365 whole foods mixes of

Brownies

pancake and waffles mixes

salad dressing

noodles sometimes (walmart stopped carring these)

Pamalas cookies

veggie cheese slices

Depending on what I need when I go I can get out of the store for $20-$32 everything else I go to Walmart or one of my local food stores to get the other groceries. Yes since I have been buying gluten free food, my buget has increased by a few dollars, but with coupons and getting things on sale then it is not so bad.

donna

ConnieA84 Rookie

I am not sure about other Countries but here in Canada you get a tax break on all the "specialty" food we have to buy on a regular basis. Keep track monthly and come tax time you can claim it on your forms. Not exactly sure what the break is as this is my first year being diagnosed, but my Lawyer informed me that you do get a break. Might want to look into it in other countries, every little bit helps..


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.

  • 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. - suek54 replied to suek54's topic in Dermatitis Herpetiformis
      7

      Awaiting dermatitis herpetiformis confirmation following biopsy

    2. - knitty kitty replied to suek54's topic in Dermatitis Herpetiformis
      7

      Awaiting dermatitis herpetiformis confirmation following biopsy

    3. - suek54 replied to suek54's topic in Dermatitis Herpetiformis
      7

      Awaiting dermatitis herpetiformis confirmation following biopsy

    4. - trents replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

    5. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      how much gluten do I need to eat before blood tests?

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

    • Total Members
      133,258
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • suek54
      Wow KK, thank you so much for all your attached info. I had a very quick scan but will read more in depth later.  The one concerning corticosteroid use is very interesting. That would relate to secondary adrenal insufficiency I think , ie AI caused by steroids such as taken long term for eg asthma. I have primary autoimmune AI, my adrenals are atrophied, no chance if recovery there. But I am in touch with some secondaries, so something to bear in mind. .  Niacin B3 Very interesting too. Must have a good read about that.  Im sure lots of questions will arise as I progress with dermatitis herpetiformis. In the mean time, thanks for your help.
    • knitty kitty
      Welcome to the forum, @suek54, I have Dermatitis Herpetiformis, too.  I found taking Niacin B3 very helpful in clearing my skin from blisters as well as improving the itchies-without-rash (peripheral neuropathy).  Niacin has been used since the 1950's to improve dermatitis herpetiformis.   I try to balance my iodine intake (which will cause flairs) with Selenium which improves thyroid function.   Interesting Reading: Dermatitis herpetiformis effectively treated with heparin, tetracycline and nicotinamide https://pubmed.ncbi.nlm.nih.gov/10844495/   Experience with selenium used to recover adrenocortical function in patients taking glucocorticosteroids long https://pubmed.ncbi.nlm.nih.gov/24437222/   Two Cases of Dermatitis Herpetiformis Successfully Treated with Tetracycline and Niacinamide https://pubmed.ncbi.nlm.nih.gov/30390734/   Steroid-Resistant Rash With Neuropsychiatric Deterioration and Weight Loss: A Modern-Day Case of Pellagra https://pmc.ncbi.nlm.nih.gov/articles/PMC12532421/#:~:text=Figure 2.,(right panel) upper limbs.&text=The distribution of the rash,patient's substantial response to treatment.   Nicotinic acid therapy of dermatitis herpetiformis (1950) https://pubmed.ncbi.nlm.nih.gov/15412276/
    • suek54
      Thank you all for your advice and the dermatitis herpetiformis article. The latter made me realise I had stopped taking my antihistamine, which I will restart today. The Dapsone has cleared the rash entirely but I still get quite a bit itching, absolutely nothing to see though. I know its notoriously hard to clear and its still relatively early days for me.  The iodine issue is very interesting. I do eat quite a bit of salt because I have Addison's disease and sodium retention is an issue. I also have autoimmune hypothyroidism, not sure how a low iodine diet would play into that? Because of my Addison's I am totally steroid dependent, I take steroids 4 x daily and cannot mount any defence against inflammation. I need to increase my meds for that. Now that I know what is wrong I can do just that if Im having a bad day. Life is very sweet, just so damn complicated sometimes! Hey ho, onwards. Thank you again for your advice.  
    • trents
      So, essentially all of the nutrition in the food we eat is absorbed through the villous lining of the small bowel. This is the section of the intestinal track that is damaged by celiac disease. This villous lining is composed of billions of finger-like projections that create a huge amount of surface area for absorbing nutrients. For the celiac person, when gluten is consumed, it triggers an autoimmune reaction in this area which, of course, generates inflammation. The antibodies connected with this inflammation is what the celiac blood tests are designed to detect but this inflammation, over time, wears down the finger-like projections of the villous lining. Of course, when this proceeds for an extended period of time, greatly reduces the absorption efficiency of the villous lining and often results in many and various nutrient deficiency-related health issues. Classic examples would be osteoporosis and iron deficiency. But there are many more. Low D3 levels is a well-known celiac-caused nutritional deficiency. So is low B12. All the B vitamins in fact. Magnesium, zinc, etc.  Celiac disease can also cause liver inflammation. You mention elevated ALP levels. Elevated liver enzymes over a period of 13 years was what led to my celiac diagnosis. Within three months of going gluten free my liver enzymes normalized. I had elevated AST and ALT. The development of sensitivities to other food proteins is very common in the celiac population. Most common cross reactive foods are dairy and oats but eggs, soy and corn are also relatively common offenders. Lactose intolerance is also common in the celiac population because of damage to the SB lining.  Eggs when they are scrambled or fried give me a gut ache. But when I poach them, they do not. The steam and heat of poaching causes a hydrolysis process that alters the protein in the egg. They don't bother me in baked goods either so I assume the same process is at work. I bought a plastic poacher on Amazon to make poaching very easy. All this to say that many of the issues you describe could be caused by celiac disease. 
    • catnapt
      thank you so much for your detailed and extremely helpful reply!! I can say with absolute certainty that the less gluten containing products I've eaten over the past several years, the better I've felt.   I wasn't avoiding gluten, I was avoiding refined grains (and most processed foods) as well as anything that made me feel bad when I ate it. It's the same reason I gave up dairy and eggs- they make me feel ill.  I do have a bit of a sugar addiction lol so a lot of times I wasn't sure if it was the refined grains that I was eating - or the sugar. So from time to time I might have a cookie or something but I've learned how to make wonderful cookies and golden brownies with BEANS!! and no refined sugar - I use date paste instead. Pizza made me so ill- but I thought it was probably the cheese. I gave up pizza and haven't missed it. the one time I tried a slice I felt so bad I knew I'd never touch it again. I stopped eating wheat pasta at least 3 yrs ago- just didn't feel well after eating it. I tried chick pea pasta and a few others and discovered I like the brown rice pasta. I still don't eat a lot of pasta but it's nice for a change when I want something easy. TBH over the years I've wondered sometimes if I might be gluten intolerant but really believed it was not possible for me to have celiac disease. NOW I need to know for sure- because I'm in the middle of a long process of trying to find out why I have a high parathyroid level (NOT the thyroid- but rather the 4 glands that control the calcium balance in your body) I have had a hard time getting my vit D level up, my serum calcium has run on the low side of normal for many years... and now I am losing calcium from my bones and excreting it in my urine (some sort of renal calcium leak) Also have a high ALP since 2014. And now rapidly worsening bone density.  I still do not have a firm diagnosis. Could be secondary HPT (but secondary to what? we need to know) It could be early primary HPT. I am spilling calcium in my urine but is that caused by the high parathyroid hormone or is it the reason my PTH is high>? there are multiple feedback loops for this condition.    so I will keep eating the bread and some wheat germ that does not seem to bother me too much (it hasn't got enough gluten to use just wheat germ)    but I'm curious- if you don't have a strong reaction to a product- like me and wheat germ- does that mean it's ok to eat or is it still causing harm even if you don't have any obvious symptoms? I guess what you are saying about silent celiac makes it likely that you can have no symptoms and still have the harm... but geez! you'd think they'd come up with a way to test for this that didn't require you to consume something that makes you sick! I worry about the complications I've been reading about- different kinds of cancers etc. also wondering- are there degrees of celiac disease?  is there any correlation between symptoms and the amnt of damage to your intestines? I also need a firm diagnosis because I have an identical twin sister ... so if I have celiac, she has it too- or at least the genetic make up for having it. I did have a VERY major stress to my body in 2014-2016 time frame .. lost 50lbs in a short period of time and had severe symptoms from acute protracted withdrawal off an SSRI drug (that I'd been given an unethically high dose of, by a dr who has since lost his license)  Going off the drug was a good thing and in many ways my health improved dramatically- just losing 50lbs was helpful but I also went  off almost a dozen different medications, totally changed my diet and have been doing pretty well except for the past 3-4 yrs when the symptoms related to the parathyroid issue cropped up. It is likely that I had low vit D for some time and that caused me a lot of symptoms. The endo now tells me that low vit D can be caused by celiac disease so I need to know for sure! thank you for all that great and useful information!!! 
×
×
  • 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.