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

Is Anyone Else Anxious About Eating During The Holidays?


Virgie

Recommended Posts

Virgie Apprentice

Hi! I am so anxious about my daughter and eating during the Thanksgiving holiday. This is her first holiday as gluten free. We have potluck one day & eat at a restaurant the next day (I hate eating out now). She is 13 and has been doing very well with shopping, reading labels, does not cheat, etc. So I am not worried that she will sneak off and have pie or anything like that. What I worry more about is cross contamination and what other people bring to the potluck. I also don't want her to feel like she can't eat anything. And she does feel that way when we eat out. Eating out is tough!! Hopefully it isn't where you live but where we live it is hard to even find a place that has even heard of gluten. We really feel the need to educate people around here.

So am I the only crazy, over protective Mom here??!!!

Happy Thanksgiving all!!! :)

Virgie

son 18 UC, EE, IBS, asthma & daughter 13 Celiac


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



Celiac.com Sponsor (A8-M):



dandelionmom Enthusiast
So am I the only crazy, over protective Mom here??!!!

Happy Thanksgiving all!!! :)

Virgie

son 18 UC, EE, IBS, asthma & daughter 13 Celiac

Happy Thanksgiving to you too! You are not the only crazy, over protective mom here; I am one too!

The idea of a potluck makes me want to cry! My DD will have a "safe snack box" with her where ever we go through all the holidays and we've adopted a "when in doubt don't eat it" policy. I'm the most worried about meals with my ILs so we're eating before going to their gatherings.

missy'smom Collaborator

For the restauraunt, call ahead and talk to the manager and plan ahead so that when you walk in the door you'll know what she's going to order, if necessary go through the manager again to place your order. If you can choose the restaurant, pick one that works with fresh, raw ingredients if possible.

For the potluck bring a dish or more to share that she can eat and make sure she gets served first or keep a portion aside for her. Ask questions about any dishes that seem simply prepared or are something that you are somewhat familiar with. I brought three dishes to a potluck once just so that I would have something to eat. It is a bit of a burden but in the end I would rather bring my own food and enjoy the social aspect of being around others than sit at home. It can take some people days to recover from even the slightest bit of gluten. It's just not worth the risk.

Joni63 Collaborator

Hi Virgie,

Sounds like your daughter is really being responsible. I give her a lot of credit at 13. I also worry about cross contamination. In fact my mom invited me and my family to go out to dinner for Thanksgiving so no one would have to cook this year. I declined. I just couldn't deal with the hastle of calling a local restaurant, which like yours is clueless in the small town I live in. Like you, I think it's not worth the risk.

I did go to my sons Boy Scout dinner that was potluck. I made a chicken/rice/broccoli casserole in case it was my only choice. I did have some ham that was in pineapple juice with brown sugar and also a few raw veggies, no dip. I made out fine and it was good to be there and not feel totally secluded from the world. But there were so many combination foods and desserts...I knew it would be too much to try and find out what was in those dishes.

I totally agree with you about educating the people in your town. Is there a local Celiac Support Group in your area. I've often thought about starting a group in my area. It is needed so badly. Just to solicit one restaurant as a group that would be willing to listen...would be so nice. I just have so many things I'm doing right now for my 2 children that unfortunately I don't have the time. I would so gladly love to see it happen though. Maybe there is a group semi-local to you that would be willing to help educate the restaurants and grocery stores in your area.

KaitiUSA Enthusiast

I'm not a mom yet but I understand where you are coming from and I know my mom feels the same way even now when everyone is used to dealing with my diet. Good luck and I'm sure it will all be great. Your daughter sounds very responsible for dealing with this for her age. There is so much good stuff we can eat so it makes it a little bit easier.

wowzer Community Regular

So far I've found eating at family functions almost worse than eating out. I survived Thanksgiving with no problems. I did have to come home to eat turkey. I took a waldorf salad, I should have also taken a dessert. I'll plan better for Christmas.

confusedks Enthusiast

Hello Virgie,

It's great to "see" you online again. I know that Thanksgiving has already passed, but for the upcoming holidays, you could maker her her own plate of food. I was going to bring a stuffed cornish game hen with a mini pumpkin pie for Thanksgiving (I ended up sick..so I didn't, but was a good idea). That way you wouldn't have to worry about CC.

I hope this helps. I hope your son is feeling okay.

Kassandra :)


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



Celiac.com Sponsor (A8-M):



Virgie Apprentice

Hi again! Well we did make it through the holiday. I made my daugher a gluten free pumpkin pie that tasted fairly good. She ate it anyway. And my hubbys brother, sister-in-law & family were excellent always asking my daughter about what she could eat and asked if she wanted to cut up the celery, and prepare other foods if she was worried about cross contamination & such. So that day went pretty good. Sunday was another story. Went out to eat and she just didn't trust eating anything so she just drank some milk. And something still probably didn't sit right with her because she didn't feel good and had the worst smelling gas ever. We really hate eating out. It just seems so hard. She has an appt. at Mayo next month & I would also like to see if she could get in to see a dietian as I am not sure she is geting all the vitamins she needs and such. Always something.

Next Monday I will have surgery on my hand. I have had carpal tunnel for 18 years and did have my right hand done 9 years ago but have been putting off the left hand. And I hope everything goes ok that morning because my son hates Monday mornings. Well mornings in general are awful for him. He usually has nausea, fatigue, & dizziness. So I hope next week he won't have that. He has been under alot of stress with school as he is taking both college & High School courses. And he missed about 20 days of school last quarter which didn't make it any easier. So I have been feeling a little stressed too and haven't been on as much lately. I have been thinking about you & your family and hoping that the diet change has helped your kiddo. Hopefully she doesn't find it as hard as my daughter does. Mine does really good with reading labels & that sort of thing. For her it is more emotional. She hates fast food commercials and yells at the TV. But she is campaigning to make people more aware of Celiac so I am proud of her for handling that so well. And she doesn't cheat which I am glad that she has no desire to cheat at all.

Well, I have to see if my kids are feeling better and ready to go to school. Hate mornings. And it is the same on the weekends too so its not that the kids hate school or anything like that. In fact daughter got on the A Honor Roll. She is a smartie (doesn't get it from me).

Take care & write when you can. I am anxious to know how everything is going with you.

Virgie

Hello Virgie,

It's great to "see" you online again. I know that Thanksgiving has already passed, but for the upcoming holidays, you could maker her her own plate of food. I was going to bring a stuffed cornish game hen with a mini pumpkin pie for Thanksgiving (I ended up sick..so I didn't, but was a good idea). That way you wouldn't have to worry about CC.

I hope this helps. I hope your son is feeling okay.

Kassandra :)

buffettbride Enthusiast

Thanksgiving went really well for us, and it wasn't even 100% gluten free. The turkey was fine and I made gluten-free stuffing and mashed potatoes and some Chebe rolls. That was what my daughter wanted.

Christmas I expect to be a bit trickier. One, because of the disappointment of not being able to eat many of the goodies readily available. We are combating this by doing a lot of baking together (my daughter is 10) and making lots of things she CAN have.

As for all the family dinners (we'll have 4 of them) we haven't figured out what we're going to do to keep those safe as we are not hosting any of them. It will probably be a combination of bringing her food with maybe 1-2 other family members we trust to make a few items gluten-free.

My daughter is also very good about not cheating because it's just so awful when she gets sick, plus, who wants to be sick on Christmas!

Darn210 Enthusiast

I think we did pretty good . . . hard to tell since my daughter is a silent celiac (I think . . . we can't possibly have gone this long without an accidental glutening).

Thanksgiving was at my Mom&Dad's. I brought a safe turkey breast to cook & share. The ham was safe (which I also cooked). I feel like I was the drill sargent in the kitchen - "No, you can't use that. Get a clean one"; "You have to use an unopened stick of butter"; "You can't have that one, it's for the kids" :lol::lol: Then, when the buffet line was ready, I announced to the crowd of 20 that my kids were going first in case the rest of them screwed everything up! :lol::lol: My family are all good sports. I know a lot of people can't get away with this without having a family meltdown, but my family does very well as long as it is handled with humour.

Virgie Apprentice

"I feel like I was the drill sargent in the kitchen - "No, you can't use that. Get a clean one"; "You have to use an unopened stick of butter"; "You can't have that one, it's for the kids" :lol::lol: Then, when the buffet line was ready, I announced to the crowd of 20 that my kids were going first in case the rest of them screwed everything up! :lol:"

That is exactly how I felt - like a drill sargent or something. I hope I don't feel like this at every holiday!! My husbands side was really pretty good. Now my Mother (I love her honestly) still thinks it can't be that bad if she eats a little bit or if she uses the same cutting board, etc. She also thinks that my daughter won't have to do this for life just for a couple of years. And I can't let the doctors talk me into everything. Sigh!! Time for more education Iguess.

We'll see how Christmas goes next.

virgie

Dramagal Newbie

This gluten free stuff is all new to me. I haven't yet gotten half my family even updated about my daughter's newly found gluten intolerance. But I'm struggling away, trying to make it work. I'm concerned about Christmas too. Do you have to call every manufacturer to find out if there may be gluten in stuff that's not on the label? Christmas is the one time of year we eat so much more packaged stuff (cookies, candies, whatever).

We've been trying to do the gluten-free diet for about a month, but my daughter still has almost constant headaches and stomach aches. Her attention span has improved, though, and she seems calmer. Could it be she's detoxifying from the gluten? Or could it be I'm not being diligent enough to ward off trace amounts of gluten she may be getting?

kevsgirl Newbie

I offered to cook thanksgiving for my family this year. I was WAY stressed over it all. I had to tell my mother not to bring anything because although she means well something always goes wrong. (We are dealing with many more food allergies as well as gluten free) 2 other family members brought a fruit salad and cranberries respectivly and both from scratch.

This is the first holiday with all these food restrictions for us. I made a turkey in the oven. I made stuffing from rice bread and olive oil and home made chicken stock in a pan on the tove. It came out so good and I was SO nervous it would be aweful! I also made several fresh veggies. The neat thing was I made an apple and a pumpkin desert. They were as close to pies as I could get without any additional stress. Everyone loved them. (I even used real fresh pumpking from a local farm!)

I cried a LOT leading up to Thanksgiving. I have to say - we just dont go out to eat anymore. It makes some people mad but it just isnt worth it! With all the dietary issues we have several of us are simply miserable because there is NOTHING we can eat out. We did once contact a restaurant ahead and go during a non-crowded time - but it was SO expensive that again - just NOT worth it. Because of our other restrictions cross contamination is such an issue that I feel nervous just being at the tables.

As for Christmas I am telling all friends and aquatances in our sphere NOT to bring any edibles to our house. That way we can avoid an uncomfortable situation from occuring. Sadly it is HARD to handle situations elsewhere and unforseen! We were at a dance class recently where a family was passing out cupcakes. They included every allergy and aversion we have. All those kids hands and clothing covered in the stuff. Some of my affected children are small. This was aweful! We had a similar run in with candy recently. Unwrapped filled chocolates were handed out to students as they left the classroom. My child ate one before I even knew they were available! The reactions lasted for the next week! It's so frustrating. So many people have no concern what so ever either - the looks I got for declining the cupcakes (and politly too). Bottom line for us - bring our own items when we leave home (obviously a royal pain) and stay home instead of going to organized gatherings - just less painful.

Best wishes all around!

Dramagal Newbie

The restaurant stuff is an issue with us. My family insists on eating out from time to time and I don't feel it's ever really "safe." (It's also too expensive, in my opinion. )It's weird that I'm the one arguing against it when I'm the one that does most of the cooking and this gives me a break! I just wish my husband would learn more about gluten intolerance so we could pull together a bit more in the same direction. Does anyone have any suggestions about how to get a spouse more in touch with gluten issues?

celiacgirls Apprentice
I just wish my husband would learn more about gluten intolerance so we could pull together a bit more in the same direction. Does anyone have any suggestions about how to get a spouse more in touch with gluten issues?

Just stick with it and he will learn. My husband didn't really get it for close to a year when I got upset over cc. Now, there have been enough times that it has happened that even he agrees, I think. At least he has stopped complaining about it. I think when your husband sees the positive change going gluten free makes, he will figure it out.

I get anxious over eating at my family's house and they are mostly gluten-free with a few special dishes for the gluten eaters. They just don't worry about cc for themselves and although they try when I am there, it is a hard habit to get into. At every one else's house, I bring my own food. Ever since I ate at Disney World, where I can tell they get the whole cc issue, I have just not eaten in a restaurant. I just get a drink.

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. - marlene333 replied to Grace Good's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Bee balm lipbalm not gluten free

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

      Related issues

    3. - Scott Adams replied to catsrlife's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      Patiently Waiting to See Results

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

      Patiently Waiting to See Results

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

      Related issues


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,265
    • Most Online (within 30 mins)
      7,748

    Midwesteaglesfan
    Newest Member
    Midwesteaglesfan
    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

    • marlene333
      To play it safe, use Vasoline Lip Therapy. No questions as to it containing gluten.
    • Mari
      jmartes, Thank you for sharing  more information with us. Most of us Celiacs whose problems do not clear up with in a few years have to decide what to do next. We can keep seeing DR.s and hope that we will get some  medication or advice that will improve our health. Or we can go looking for other ways to improve our health. Usually Celiac Disease is not a killer disease, it is a disabling disease as  you have found out. You have time to find some ways to help you recover. Stay on your gluten-free diet and be more careful in avoiding cross contamination . KnittyKitty  and others here can give you advice about avoiding some foods that can give you the gluten auto immune reaction and advice about vitamins and supplement that help celiacs. You may need to take higher doses of Vit. B12  and D3.  About 20 years before a Dr. suggested I might have Celiac disease I had health problems that all other Dr said they could not identify or treat. I was very opposed to alternative providers and treatments. So many people were getting help from a local healer I decided to try that out. It was a little helpful but then, because I had a good education in medical laboraties she gave me a book  to read and what did I think. With great skeptism I started reading and before I was half way through it I began using the methods outlined in the book. Using those herbs and supplements I went from hardly able to work to being able to work almost fulltime. I still use that program. But because I had undiagnosed celiac disease by 10 years later some  of my problems returned and I started to loose weight.    So how does a person find a program that will benefit them? Among the programs you can find online there are many that are snake oil scams and some that will be beneficial. by asking around, as I did. Is there an ND in your area? Do they reccomend that person? If you would like to read about the program I use go to www.drclark.net   
    • Scott Adams
      It's unfortunate that they won't work with you on this, but in the end sometimes we have to take charge of our own health--which is exactly what happened to me. I did finally get the tests done, but only after years of going down various rabbit holes and suffering. Just quitting gluten may be the best path for you at this point.
    • catsrlife
      My doctor didn't take the time to listen to anything. I don't even think she knows what it means. She is more concerned about my blood pressure that is caused by her presence than anything else and just wants to push pills at me. The so-called dermatologist wouldn't do a skin test. she prescribed all of these silly antihistamine skin meds. This lady didn't even know what she was talking about and said "they never turn out as celiac, they usually just say it's dermatitis so here's your meds," just like my regular quack. I'm trying to change insurance companies at the moment and that has been a battle because of red tape, wrong turns, and workers having wrong phone numbers. What a joke! The allergy blood days say I have a wheat allergy of .31. Hopefully it's just that and until I find a decent doctor and dermatologist, I'll just lay off the wheat anyway, since it gives me asthma, high blood sugar, and joint pain. So frustrated at this point. The rash on my back of arms/elbows is mostly gone. Both calves and chest have started up. smh. It comes and goes. It fades faster now, though, although my forearms still produce one or two bumps on each side. The itching has calmed down a lot except for the bump area. I have dry skin to begin with so anything affecting it just makes it crazy. i'm never going to eat wheat again. I don't care if they need it to produce results or if it is just an intolerance, allergy, or celiac. It gives me hell.
    • Jmartes71
      I had the test done by one of the specialist through second pcp I had only a few months because he was saying I wasn't.Even though Im positive HLA-DQ2 .My celiac is down played.I am with new pcp, seeing another girl doctor who wants to do another breathe test next month though Im positive sibo this year.I have high blood pressure not sure if its pain from sciatica or sibo, ibs or hidden gluten. Im in disability limbo and I should have never been a bus driver because im still suffering and trying to heal with zero income except for my husband. This isnt fare that my health is dictating my living and having ti beg for being revalidation of my disregarded celiac disease. Its an emotional roller coaster I don't want to be on and the medical made it worse.New pcp new gi, exhausted, tired and really fed up. GI doctor NOT girl..
×
×
  • 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.