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

Please Help


Guest chetalrim

Recommended Posts

Guest chetalrim

I'm in the process of being tested for celiac disease, but my doctor has indicated that regardless of the results, she'll have me going strictly gluten free anyway.

I do the vast majority of the cooking in the house, and my husband obviously has certain things that he loves eating that I won't be able to. We also have 5 children between us that I need to cook for as well.

I know that going gluten free is probably going to make me feel loads better, but how on earth do I cook dinner for me, my husband and the kids without cooking 3 different meals? Our children range between 8 weeks - 9 years of age, so I pretty much have my hands full as it is! How strict do you really have to be? We can't afford new cookware etc just for me, plus it will double the dishes I have to do anyway.

I just don't want to be a big inconvenience for my family. My husband knows I have to be gluten free soon, but I really don't think he completely understands what that will involve. I don't even fully understand it yet!! At first I was so excited at the prospect of feeling better, now I'm thinking of the whole thing with a huge sense of trepidation. *sigh* How does everyone with families cope?


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



Celiac.com Sponsor (A8-M):



Wolicki Enthusiast
I'm in the process of being tested for celiac disease, but my doctor has indicated that regardless of the results, she'll have me going strictly gluten free anyway.

I do the vast majority of the cooking in the house, and my husband obviously has certain things that he loves eating that I won't be able to. We also have 5 children between us that I need to cook for as well.

I know that going gluten free is probably going to make me feel loads better, but how on earth do I cook dinner for me, my husband and the kids without cooking 3 different meals? Our children range between 8 weeks - 9 years of age, so I pretty much have my hands full as it is! How strict do you really have to be? We can't afford new cookware etc just for me, plus it will double the dishes I have to do anyway.

I just don't want to be a big inconvenience for my family. My husband knows I have to be gluten free soon, but I really don't think he completely understands what that will involve. I don't even fully understand it yet!! At first I was so excited at the prospect of feeling better, now I'm thinking of the whole thing with a huge sense of trepidation. *sigh* How does everyone with families cope?

I feed my kids what I am eating, most of the time. All fresh veg,, fruits and lean meats with nuts once in a while. My system hasn't healed enough to tolerate any grains, and I had to give up dairy and peanut butter. But I will occassionally make them their mac and cheese, or peanut butter sammies- I just make theirs on regular bread.

It's not that hard and the benefit is that your whole family will be eating healthier :D Just ask them all to be patient while you figure it out!

runningcrazy Contributor

Just make a few changes to many meals, and your family probably wont even know.

Homemade mac and cheese with rice pasta and cornstarch to thicken your whitesauce.

Spaghetti with rice or corn/quinoa pasta.

Some meals are naturally gluten free: steak with safe sauce, salad no croutons, and a baked potato.

Burgers, just use your own bun.

Breakfast for dinner: gluten free pancakes(non-celiacs would like them), eggs, bacon, toast for them, etc. Whatever you like.

When it comes to meatballs or meat loaf, gluten free bread chopped up or quinoa flakes do the trick.

Tacos with safe seasoning and corn tortillas or hard shells(be sure the ingredients are safe)

Make a gluten free crust using a mix, and make homemade pizza,no one will know.

Spanish rice and chicken/pork chops

If you look more towards easy ways to switch things,it doesnt seem so bad. Its easy to switch to a different pasta, skip the croutons and use a safe dressing, etc.

Good luck!

Darn210 Enthusiast

At the beginning it does seem overwhelming . . . after you've been at it for awhile, you'll realize it's not so bad.

We have a mixed kitchen. However, all cooking and baking is gluten free. It's not that hard to convert your family favorites to gluten free. Many times it's a matter of switching brands on some of your ingredients (now we use La Choy soy sauce and Baby Rays BBQ sauce). Meals can be "supplemented" for the gluten eaters with a hamburger bun here or sandwich bread there.

I did not get all new cookware. I got two new nonstick skillets (my old ones were a bit scratched up and couldn't be scrubbed clean), a new cutting board, a new pasta strainer, a new cookie sheet and a new toaster.

Gluten items (cereal, breads, cookies) are segregated in their own cabinet.

If you've got some recipes that you need help converting, this is the perfect place to ask. Lots of people here have already been through this process and can give you good ideas on substitutions.

. . . and welcome to the board :D

GottaSki Mentor

Our family dinners are gluten-free...we started with meat, vegies and either rice/potato and have now replaced ingredients in most of our old favorites. It will take some effort, but I can tell you it becomes much easier within a short time.

We do still have gluten cereals, breads and flour tortillas for my gluten eaters, but most of our food has become gluten-free. There are many posts about sharing kitchen with gluten eaters...separate cutting boards, toaster and condiments (butter, mayo, jams, pnut butter, etc). We mark our gluten-free items with small bright green circle stickers.

Good luck to you!

-Lisa

Guest chetalrim

Wow, thankyou so much everyone. I think I'm letting my worries run away with me. It's very reassuring to know there will be a way to manage it and that so many others cope just fine. I will definitely be doing a few searches for hints and tips!!! Probably best to try and get my head around it now, rather than when I have to start my gluten-free diet.

Thanks for the terrific support :D

ranger Enthusiast

Husband eats gluten- I don't. The other night, we had Mac and Cheese made with Tinkinyada rice pasta and cheese sauce thickened with cornstarch. Dh loved it. I make 8 in. pizza crust for me, freeze them, and buy him a frozen or delivered pizza. He eats glutteny things outside of the house, but our shared meals are almost always gluten-free. When we have burgurs, he has regular buns, I have gluten-free buns in the freezer. It's more work, but doable. And, we eat healthier now. Good luck.


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



Celiac.com Sponsor (A8-M):



hannahp57 Contributor

My kitchen is shared also. we have separate cereal, crackers, tortillas, and bread. eveything else is gluten free. when i cook i can eat it. on the rare occasion i make something gluteny specifically for him, the kitchen is cleaned BEFORE and AFTER it is made. before so i can see all counter space and will know where contamination is. if you have alot of things on your counter and you spill flour it may hide and remain there awhile. we have a four slice toaster that has not glutened me yet! i have found glass dishes are the safest. just make dinner like always with gluten free ingredients substituted in and have the whole family eating one meal. it is unnecessary to make multiple meals, our food is just as healthy and most things are just as yummy. i would continue to buy regular bread just becuase the gluten-free flours are so expensive

Guest chetalrim

Thanks, I've been researching quite a bit and I think most of the time I can substitute gluten free ingredients for what I already use. We eat lots of salad (so that's easy!) and stir fries, so as long as my sauce ingredients are gluten free, it should be all good! I am definitely going to try and cook just one meal as per normal, and sometimes make something gluteny for the kids.

Ruthie73 Newbie

Thumbs up to you! I was in a similar positiona year ago, and it is daunting/ a bit depressing at first, but once you get used to shopping for the right ingredients - say your gluten-free pasta and bread, etc; and swap your gluteny basic cooking ingredients like flour,soy sauce and stock cubes for gluten-free variants, etc, it all gets easier... and no-one notices the difference in the taste. :D

One tip we discovered for cooking pasta whilst on our camping hols this year - we only had two gas rings, so one was cooking the gluten-free sauce, the other for the water - problem: we all wanted to eat at the same time. Cooked my pasta first (too expensive for the whole family to eat it!) then scooped it out onto a plate and covered to keep warm, then put their reg pasta into the same water. No time issue, as the sauce was still cooking anyway!... Just have to make sure you have loads of water, as it does get a bit starchy or something from the gluten-free pasta. Result: less washing up! lol

Good luck!

x

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.