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

Has Anyone Done This?


LuvMoosic4life

Recommended Posts

LuvMoosic4life Collaborator

Since I've been gluten-free, a few of my family members who are really into cooking and baking want to make gluten-free food for me. Although they have good intentions, I'm sure they arent aware of the CC issue, and even if they are the chance of CC is very likely since they bake and cook with gluten food in thier kitchens all the time.

I was thinking of typing up just a 1 to 2 page info sheet about celiacs/gluten intolerance and explaining the precautions /things to know before baking or cooking for celiacs. I figure I can hand it out to my family members before they try to make something for me. :lol:

I know my aunt has talked about making cookies for me, but I would hate for her to make them w/o prior gluten-free baking knowledge b/c I would feel bad declining eating them in fear of cc. Or worse, eating them and having a reaction. My reactions arent always horrible, it depends, sometimes I have no reaction, but I just choose to stay completely away from gluten, the results have been amazing, I'm so grateful I found out about all of this...


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



Celiac.com Sponsor (A8-M):



home-based-mom Contributor
Since I've been gluten-free, a few of my family members who are really into cooking and baking want to make gluten-free food for me. Although they have good intentions, I'm sure they arent aware of the CC issue, and even if they are the chance of CC is very likely since they bake and cook with gluten food in thier kitchens all the time.

I was thinking of typing up just a 1 to 2 page info sheet about celiacs/gluten intolerance and explaining the precautions /things to know before baking or cooking for celiacs. I figure I can hand it out to my family members before they try to make something for me. :lol:

I know my aunt has talked about making cookies for me, but I would hate for her to make them w/o prior gluten-free baking knowledge b/c I would feel bad declining eating them in fear of cc. Or worse, eating them and having a reaction. My reactions arent always horrible, it depends, sometimes I have no reaction, but I just choose to stay completely away from gluten, the results have been amazing, I'm so grateful I found out about all of this...

Check out this thread. There is a pretty good list there! :P

Open Original Shared Link

lpellegr Collaborator

It's hard to say no when they have such good intentions, isn't it? But I always turn it down as nicely as I can and explain that it's such a specialized way of eating that it takes a specially prepared kitchen to avoid hurting you. Explain that even their favorite wooden spoon can hurt you if they stir that gluten-free brownie mix with it, or if they used the same spoon to scoop sugar after using it in flour a long time ago that the tiny bits of flour left in that sugar can hurt you. My sister made potato salad with perfectly gluten-free ingredients, but her mayo jar had been used for family sandwiches and sure enough it got me. Tell them how much you appreciate the thought, and would LOVE to be able to say yes, but your insides have taken a beating and you just can't take that chance. Tell them, if they are determined to treat you somehow, that you'll eat any packaged food that is labeled "gluten-free", or suggest something that you know is gluten-free like a specific type of ice cream or a chocolate bar.

So yes, you might want to give them an info sheet, but don't expect them to fully read/understand/believe it. Be kind to them and accept what you can from them and give them suggestions so that they can continue to feel they are doing something nice for you, even if it isn't home cooking. They mean well, but they don't have to suffer your symptoms.

LuvMoosic4life Collaborator
It's hard to say no when they have such good intentions, isn't it? But I always turn it down as nicely as I can and explain that it's such a specialized way of eating that it takes a specially prepared kitchen to avoid hurting you. Explain that even their favorite wooden spoon can hurt you if they stir that gluten-free brownie mix with it, or if they used the same spoon to scoop sugar after using it in flour a long time ago that the tiny bits of flour left in that sugar can hurt you. My sister made potato salad with perfectly gluten-free ingredients, but her mayo jar had been used for family sandwiches and sure enough it got me. Tell them how much you appreciate the thought, and would LOVE to be able to say yes, but your insides have taken a beating and you just can't take that chance. Tell them, if they are determined to treat you somehow, that you'll eat any packaged food that is labeled "gluten-free", or suggest something that you know is gluten-free like a specific type of ice cream or a chocolate bar.

So yes, you might want to give them an info sheet, but don't expect them to fully read/understand/believe it. Be kind to them and accept what you can from them and give them suggestions so that they can continue to feel they are doing something nice for you, even if it isn't home cooking. They mean well, but they don't have to suffer your symptoms.

thats so true. I know they still wont completely understand it,and it's a bumber :( but at least I am spreading awareness :)

Mom23boys Contributor

I haven't done it.

My family would feel free to make substitutions. "I don't know where to buy Bob's oats, these here in the bulk bin will work the same."

or then there is the aunt who gets her nose out of joint "What!?! You are saying that I don't clean my utensils good enough for you?!? I take great care in cleaning my highly porous flour utensil. It will be clean enough for the gluten flour too!!".

Between clueless and insulted I'd have them all mad. Thankfully one of our professionals said "you may not eat anything you did not prepare or open at certain functions".

Gaye of PA Apprentice

I agree with the others--no matter how carefully you would write it, first you can't depend on people reading it correctly--that's just the way people are. Secondly, you can't ever be completely sure they didn't cut corners (or forget) somewhere along the line.

Just today at the family reunion, a relative was happy because she thought we might be able to eat her pie. I was very confused. "Well...that's a wheat-flour crust, right?" Her reply was "Yes, but can't you just scrape it off--the filling is gluten free." :o

So eventually, everyone will learn how it really is for us, one incident at a time. I just lightly exclaimed, "Oh my, no! Even a crumb would be harmful. Even your pan and utensils, if they've been used for wheat before this, could contain trace amounts of gluten."

This seemed to immediately help her understand, without a lot of explantion.

munchkinette Collaborator

I've considered doing this a number of times for my dad and stepmother. The first year I had to stop my stepmother as she was about to put Wondra on my separate piece of chicken. She gets it now, but we pretty much just get into the habit of going to restaurants, or eating holiday dinners with my mom then going to their house for dessert.

My mother seems to do ok- she calls me when she's at the grocery store, and she plans meals ahead when both my brother and I are coming down. (He's gluten-free as well.) She's no stranger to allergies and cooking though- her bf has a bad egg allergy.


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



Celiac.com Sponsor (A8-M):



Wonka Apprentice
Since I've been gluten-free, a few of my family members who are really into cooking and baking want to make gluten-free food for me. Although they have good intentions, I'm sure they arent aware of the CC issue, and even if they are the chance of CC is very likely since they bake and cook with gluten food in thier kitchens all the time.

I was thinking of typing up just a 1 to 2 page info sheet about celiacs/gluten intolerance and explaining the precautions /things to know before baking or cooking for celiacs. I figure I can hand it out to my family members before they try to make something for me. :lol:

I know my aunt has talked about making cookies for me, but I would hate for her to make them w/o prior gluten-free baking knowledge b/c I would feel bad declining eating them in fear of cc. Or worse, eating them and having a reaction. My reactions arent always horrible, it depends, sometimes I have no reaction, but I just choose to stay completely away from gluten, the results have been amazing, I'm so grateful I found out about all of this...

A woman from the Delphi Celiac Forum has just done this recently. Here is what she has written:

There are long lists of ingredients that are allowed and those that are not allowed on a gluten-free diet. In reality, since the Food Allergen Labeling and Consumer Protection Act (FALCPA), took effect in January 2006, label reading is simple. FALCPA requires that wheat always be labeled clearly, but it does not cover barley, rye, or oats.

This document discusses products that would be gluten free in ingredients, and does not speak to the potential of contamination with gluten grains during processing and manufacturing. If you are concerned about potential manufacturing contamination, contact the company for more information on their manufacturing practices. When in doubt, call the company or do not use the product.

For all meat and poultry products: any plant protein (wheat, barley, rye) will be listed. Meat and poultry are regulated by the USDA, and on 1, 1990, FSIS published the final rule, Ingredients That May Be Designated as Natural Flavors, Natural Flavorings, Flavors, or Flavorings When Used in Meat or Poultry Products. The rule stated that any plant protein that was added to a product must be listed. Therefore, for any meat product, read the label, and if the words

MyMississippi Enthusiast

I just tell friends and relatives "Don't even THINK about trying to cook for me - "

I tend to my own food--- and as much as possible don't even talk about it . If someone says anything, I just say, I'm allergic to wheat (which I am )---- and change the subject . Not gonna live my life around food issues. :)

rick-spiff Rookie
6. Beer---beer is made with barley and should be avoided

Beer is made with barley, and therefore not safe on a gluten-free diet. If a product is made with gluten free beer, it would be safe, but as of June 2008, I've never encountered a commercially available product made with gluten-free beer.

RedBridge is a sorghum based beer and they have it at supermarkets that have a gluten free section ie red meyers, yolks, market of choice, whole foods, trader joes, also albertsons, wal-mart

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,957
    • Most Online (within 30 mins)
      7,748

    Dogdad21
    Newest Member
    Dogdad21
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.