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Thanksgiving And Family...


Trudyjerry

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GFinDC Veteran

Hi BC,

Hashimoto's is associated with celiac disease. They are both autoimmune condtions. The odds of having another autoimmune condition are higher for people with celiac disease too. There are several people with Hashimoto's Thyroiditis on the forum.


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Cara in Boston Enthusiast

My son and I are the only two gluten free in the entire extended family (although many others probably should be . . . ) and he is so sensitive that he cannot eat anything prepared in someone else's kitchen - even if no gluten ingredients are used. I usually cook a gluten free "Thanksgiving" earlier in the week to have at home with my immediate family and we save leftovers to bring as our meal to the "real" Thanksgiving. I try to make similar foods so at least at the table, it looks like we are eating what everyone else is having. (but we would both probably prefer lasagna or something)

I found that bringing a side dish to share doesn't always work out because unless we get to it first, it almost always gets contaminated somehow (there are about 40 people there, so someone always switches a serving spoon or something . . .)

We each have one of these:

Open Original Shared Link

and it is AWESOME. It is pretty compact, so whipping it out to plate our dinner is usually quick and inconspicuous. We've even used them at formal weddings and other functions. They keep food hot for HOURS. Even when we get home (7-8 hours later) the leftovers are still warm.) They hold plenty of food. Sometimes I just open one and can fill both our dinner plates.

No one should feel weird bringing their own food. Expecting the host to be able to safely prepare food for you (in my opinion) is rude. You are doing what you need to do to stay healthy and you are not creating any extra work or stress for anyone else.

I also always bring one or two desserts to share. That way there is something on the dessert table for my 7 year old to choose and he doesn't feel like he is missing out on anything.

To be honest - it has been GREAT bringing our own meal. Everything is made the way we like it!

Cara

ButterflyChaser Enthusiast

I felt very reassured reading all this, and I think Cara expressed my feelings well in saying that expecting others to cook in compliance with your restrictions is rude.

I just called my friends and told them, and they said it wasn't a problem, and that they had had some family members who had had to "bring their own," even if that person wouldn't be there this year. So now I only have to device some mini and portable Thanksgiving menu that can survive some travelling...

Trudyjerry Rookie

I would never invite anybody into my home, knowing that they have dietary restrictions without being willing to make some concessions. Personally, I think that it's rude to invite someone under such circumstances and thinking that they would not bring something safe to eat and be willing to make themselves sick.

kareng Grand Master

I would never invite anybody into my home, knowing that they have dietary restrictions without being willing to make some concessions.

that works well for someone who can't have dairy. You can make baked potatoes instead of Au Gratin. They can have the asparagus but not the broccoli with cheese. For Celiacs who need to be sure there isn't a crumb of gluten, it unrealistic to expect them to buy new muffin tins, colanders, cutting boards, mayo, etc.

My SIL is coming over. she is extremely allergic to cats. Gracie will be in the basement and my SIL said she would be fine using a wooden or leather chair ( cat hair not sticking to it). that is a reasonable accommodation. if she expected that I get rid of the cat and get new furniture, that would be a bit much.

  • 4 weeks later...
Hala Apprentice

Thank you! I feel a bit better now. Though I have improved, I still struggle not having to justify why I eat the way I do. It is a very charged topic for me, because at the onset of my autoimmune disease no one - friends, doctors - believed I was sick and they just insisted I had an ED, and I "ate like a rabbit" - because eating leafy greens and simple food is part of the cultural heritage of the poor, rural area I come from. :(

Even if I am overweight now, and having always been known as a connoisseur and a great cook, I still feel like I have to justify myself, probably because such misconception was, in my case, almost lethal, because they let me get to a BMI of 13 before someone did blood tests.

I think I need to stop apologizing because I have auto-antibodies...

Hi, sorry to drag up an old post, but I was wondering how long it took until you started to gain weight?

My weight dropped really dramatically before I was diagnosed with coeliac disease. I've been gluten-free for around a month now and I'm still not gaining much weight! I have a BMI of 13 too and I'm scared :(

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    • trents
      This is a common experience across the board with various brands of gluten-free bread products. Prices go up, size goes down. Removal of the egg component may be for the purpose of cost-cutting related to bird flu supply shortages or it may be catering to those with egg allergy/sensitivity, fairly common in the celiac community.
    • HAUS
      Living with Coeliac Disease since birth, Bread has always been an issue, never too nice, small slices and always overpriced, But Sainsbury's Free From White Sliced Bread seemed to me to be an exception with it's large uniform 12 x 12cm slices that had the bounce, texture and taste of white bread even after toasting with no issue that it was also Milk Free. Unfortunately Sainsbury's have changed the recipe and have made it 'Egg Free' too and it has lost everything that made the original loaf so unique. Now the loaf is unevenly risen with 8 x 8cm slices at best, having lost it's bounce with the texture dense and cake like after toasting resembling nothing like White Bread anymore. Unsure as to why they have had to make it 'Egg Free' as the price is the same at £1.90 a loaf. Anyone else experiencing the same issue with it? - also any recommendations for White Bread that isn't prescription? / Tesco's / Asda's are ok but Sainsbury's was superior.
    • Mari
      Years  ago a friend and I drove north into Canada hoping to find a ski resort open in late spring,We were in my VW and found a small ski area near a small town and started up this gravelled road up a mountain. We  got about halfway up and got stuck in the mud. We tried everything we could think of but an hour later we were still stuck. Finally a pickup came down the road, laughed at our situation, then pulled the VW free of the mud. We followed him back to the ski area where where he started up the rope ski lift and we had an enjoyable hour of skiing and gave us a shot of aquavit  before we left.It was a great rescue.  In some ways this reminds me of your situation. You are waiting for a rescue and you have chosen medical practitioners to do it now or as soon as possible. As you have found out the med. experts have not learned how to help you. You face years of continuing to feel horrible, frustrated searching for your rescuer to save you. You can break away from from this pattern of thinking and you have begun breaking  away by using some herbs and supplements from doTerra. Now you can start trying some of the suggestions thatother Celiacs have written to your original posts.  You live with other people who eat gluten foods. Cross contamination is very possible. Are you sure that their food is completely separate from their food. It  is not only the gluten grains you need to avoid (wheat, barley, rye) but possibly oats, cows milk also. Whenever you fall back into that angry and frustrated way of thinking get up and walk around for a whild. You will learn ways to break that way of thinking about your problems.  Best wishes for your future. May you enjpy a better life.  
    • marion wheaton
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    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
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