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

I Just Want The Holidays To Be Over


alex11602

Recommended Posts

alex11602 Collaborator

Normally I wouldn't complain in the least about not being able to eat everything because I am so grateful that I don't feel sick all the time, but this is our first holiday that has alot of things served which we can not eat. I am not sure if I can deal with the holidays this year, especially Thanksgiving...we always go over to my mom's house, no matter what since it is tradition and I guess she serves the normal food. There is turkey, mashed potatoes, corn, green bean casserole, regular stuffing, sweet potato stuffing, sweet potatoes, sauteed mushrooms and cranberry sauce with pumpkin pie, sweet potato pie and apple pie for dessert. The only things I really ate were the regular stuffing, sweet potatoes, cranberry sauce and the pumpkin and sweet potato pies...none of which I can eat this year:(

Eight months ago I just jumped right into gluten free eating and I haven't really had a problem with it, but now I am dreading the holidays and end up crying about it almost everyday which is completely ridiculous. I really want to see my family, we live really close to them but holidays are family time and it's pretty much a rule that we have to be there and I'm just unsure if I can deal with it this year.

I have tried to think of different options like not going, bringing my own food or eating before we go, but none of them are going to be options for a holiday meal. I tried talking to my husband about it but he doesn't understand why I can't just say we aren't going...my grandmother would be extremely upset and she is getting older so I'm just not sure I should do that to her.

I'm sorry, I just had to vent and I'm just not sure what to do right now.


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



Celiac.com Sponsor (A8-M):



DonnaMM Explorer

I don't know what job you have but I work as a nurse and purposely work thanksgiving (because that is the holiday where my family serves the most glutinous foods) as an excuse to get out of family dinner, but I know jot everyone has the ability. I assume because they are family they understand your medical needs. I would recommend asking your mom if you could help make thanksgiving dinner and do it gluten free style. Don't bother to tell the rest of your family they probably would not even be able to tell the difference. Plus it would be a great chance to spend time with your mom and she would probably love the help. Good luck and happy holidays

alex11602 Collaborator

I don't know what job you have but I work as a nurse and purposely work thanksgiving (because that is the holiday where my family serves the most glutinous foods) as an excuse to get out of family dinner, but I know jot everyone has the ability. I assume because they are family they understand your medical needs. I would recommend asking your mom if you could help make thanksgiving dinner and do it gluten free style. Don't bother to tell the rest of your family they probably would not even be able to tell the difference. Plus it would be a great chance to spend time with your mom and she would probably love the help. Good luck and happy holidays

I don't work right now and they don't take being gluten free seriously at all. It's a very small family get together...my husband, my daughters and I going over to my mother's house which is my mom, dad, sister and grandmother. We were only diagnosed by dietary response so we are stuck. And no one is allowed to help my mother...she doesn't like having people in the kitchen with her since it just makes things more difficult for her. Thank you though!

DonnaMM Explorer

I am sorry that your family is not as supportive that definitely makes it harder. I know it is not what you want but it appears your husband is more understanding of your dietary needs so you could just have a romantic thanksgiving dinner with the two of you. For the experience with my husband he is not too fond of family get togetheris and would rather it be intimate. You could also make yourself your own little thanksgiving plate to bring but that may you're your mothers feelings a little bit.

DonnaMM Explorer

And be sure to bring a gluten free dessert to share with everyone!

alex11602 Collaborator

I am sorry that your family is not as supportive that definitely makes it harder. I know it is not what you want but it appears your husband is more understanding of your dietary needs so you could just have a romantic thanksgiving dinner with the two of you. For the experience with my husband he is not too fond of family get togetheris and would rather it be intimate. You could also make yourself your own little thanksgiving plate to bring but that may you're your mothers feelings a little bit.

My husband is extremely understanding and I am so grateful for that. He went gluten free with me and our daughters and found that he felt better too so he definitely understands. I guess there are alot of things to think about in the next few weeks.

NateJ Contributor

yeah, I'm not looking forward to this either. I'm thinking of taking my kids to NYC just for a few days to see the parade and avoid gluten. I'm not sure how else to deal with it. I'm not going to sit and watch my family cram themselves full of poison while I eat fruit. no thanks.


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



Celiac.com Sponsor (A8-M):



wjp Newbie

Last Thanksgiving was my first gluten free Thanksgiving. I did have everyone at my house and yes it was totally gluten free. Maybe you can cook a mini-thanksgiving dinner on Wednesday evening and take some leftovers for you the next day. There are some wonderful gluten free stuffing recipes out there. It doesn't have to be huge meal but maybe some of your favorite foods. Mom will have to get over it if she gets offended by you not eating her food. Make sure you make a good dessert - maybe even one to take on Thursday with you. I have a great recipe for banana bread and banana pudding. The banana pudding one would be large enough for everyone. I know last Thanksgiving I was nervous about everyone eating gluten free but it turned out great. Good luck!!!!

melikamaui Explorer

I agree with Wjp. Why not make your own super yummy gluten-free dinner and bring it? There are some fantastic recipes online. I made my first ever gluten-free thanksgiving last year and it was a huge success! My family agreed that some of the dishes were actually better than their gluten filled counterparts! Make everyone jealous with your mouth watering gluten-free meal. :D

pricklypear1971 Community Regular

To the OP....

Perhaps what your Mom needs is to see you not eat her food. Perhaps that will knock some sense into her? I doubt letting you help her cook would be the end of her world. She'll learn. And if she doesn't-oh we'll. Move on and find other things to talk about.

I'd go - Thanksgiving is about more than the meal...,but I'd take my own food! Get a turkey breast and cook it the night before - make your own quick versions of whatever you like and pack it and take it and eat it. Yum yum.

rainer83 Newbie

I'm sorry you have to go through that :(

I know exactly what you're going through. I've been gluten free for 2 years and I haven't had a Thanksgiving dinner with my family since. My sister and I don't get along at all, we don't speak and it goes beyond rivalry to a down right hatred. She uses the celiac to her advantage during the holidays. She opts to make the dinners for Easter and Thanksgiving, and makes nothing I can eat. I volunteer to make something and she gets angry and says it will taste gross and no one will eat it. I've spent my last 2 Thanksgivings and Easters alone because of her and her attitude towards me. It's not easy at all.

kareng Grand Master

We have everyone over here. Pain in the behind for me but I know what all the food is. Even bigger pain this year because my mom has to be super low sodium. My dad suggested I not make the really yummy scalloped potatoes because they are so high in sodium. She wouldn't care if she can't eat the green beans but she really likes the potatoes. I can relate to having to watch people eat yummy stuff I can't.

SilverSlipper Contributor

Some of our family members get it and some do not. Ironically, my dad and step-mom are the worst and she is diagnosed with celiac disease (she has DH, but no stomach problems). We decided last year to avoid family holidays during meals. We go visit at other times.

This year I'm preparing Thanksgiving dinner and inviting everyone over here. It will be quite a bit of work, but I can't wait to see my daughter's face when the meal is ready!

Takala Enthusiast

Agree, if you must travel to visit the glutenoids, cook your own dinner before and sit down in a leisurely fashion and enjoy it on Tues or Wednesday. Then take leftovers on a plate for you to eat off of during the "event."

All of the things you listed as liking to eat, can easily be made gluten free. In fact, "stuffing" is the only real use for certain types of commercial rice/tapioca gluten-free breads, besides doorstops and wheel chocks. :P I don't even use bread in stuffing, I use pecans and mushrooms. Some traditions use cornbread or wild rice. If you don't like to make pie shells, you can buy frozen pre made gluten free ones, or get a boxed mix which just needs egg, "butter," and water added. Cranberry sauce is ridiculously easy to make in advance, and then keeps in the refrigerator a long time. If you need help substituting, go to the baking/cooking forum and ask. If you aren't doing dairy or eggs, there ARE other ingredients which work.

Most people, when presented with a loaf of gluten-free banana- almond meal bread on the counter pre sliced, with the piece you need already taken off for safekeeping, will eat it without a qualm. They'll eat anything, really, as long as it's halfway decent. Either butter, cheese, honey, or garlic and olive oil fixes most things. ;)

If Mother doesn't like it, too bad. She is just going to have to get over herself. This is about being social, not about getting sick because you're pretending you aren't what you are.

Roda Rising Star

Awhile ago hubby recieved an invitation to a pig roast. He debated even telling me about the invitation, because he knows that our two boys and I can not eat the food. I told him to accept the invitation because I want to socialize with people and that we rarely do anything. My husband the butcher, is bringing me home a pork butt and I am going to smoke it and make pulled pork. I am going to take that and some sides for the boys and I to eat while hubby eats the food at the pig roast. Most people won't notice since the pork will be similar. However, this is a lot different than the intimate dinner with family. I think you should go and have a nice holiday visit with grandma and your parents. Cook a small turkey breast or small whole chicken the day before with all the trimmings that you normally would have at your parents (gluten free of course) and take it and enjoy yourself. Your family might take it more seriously if you don't eat their food. This could end up positive if they take note and ask questions on how to handle your food in the future.

We usually stay home for the holidays because of my husbands and my jobs. My family is 560 miles away and my husbands is 250 miles. We can't make a day trip. It's usually just the four of us so no issues there.

ravenwoodglass Mentor

Bring your own food, a cornish game hen stuffed along with a couple of sides or leftovers from a 'just your family' Thanksgiving meal the day before will make sure you have something safe to eat.

The point of Thanksgiving is to be thankful and having been diagnosed and recovering your health is one real big thing to be thankful for this year. I hope you are able to enjoy the holiday safely.

rana Rookie

Last year I got roped into an out of town Thanksgiving with my family, while normally this would be exciting I couldn't help but dread it a little, it seemed like there was no way I could get away gluten free or enjoy myself since I'd be worried the whole time. A day or two before we left I had my own personal Thanksgiving, made everything I wanted gluten free in my safe kitchen, and sat down and ate it. I then packed a cooler with leftovers and put together a really nice plate so when I got to my cousin's house I simply had to reheat it and sit down and eat. This worked out great. No one even noticed I had a different plate than them, I already had Thanksgiving out of my system so the pressure was off to try and enjoy myself. A little more work, but well worth it.

Its a shame your immediate family isn't more understanding, I'm appalled at some of these replies and what people have to deal with. I am so sensitive to gluten that I wouldn't eat at a relatives house even if they were kind enough to make the meal gluten free, so it sort of lets them off the hook in the first place...

catsmeow Contributor

I'm not going to sit and watch my family cram themselves full of poison while I eat fruit. no thanks.

It grosses me out too, the way people cram the gluten (rat poison) into their pie holes like gluttens without a care in the world...yuck <_<

catsmeow Contributor

Do you have a local Celiac group near you? We have the Gluten Intolerance Group of Central and South Texas. We are having a gluten-free Thanksgiving potluck on the Saturday before Thanksgiving here in San Antonio. If anyone is near here, please join us. This yearly potluck is how I cope with Thanksgiving. Since I can eat everything there, it gets the whole deprived feeling thing out of my system. I think it's really healthy to meet with other gluten free people and celebrate together. In fact, it's therapeutic. We get to feel normal for a day. :)

jswog Contributor

Do you have a local Celiac group near you? We have the Gluten Intolerance Group of Central and South Texas. We are having a gluten-free Thanksgiving potluck on the Saturday before Thanksgiving here in San Antonio. If anyone is near here, please join us. This yearly potluck is how I cope with Thanksgiving. Since I can eat everything there, it gets the whole deprived feeling thing out of my system. I think it's really healthy to meet with other gluten free people and celebrate together. In fact, it's therapeutic. We get to feel normal for a day. :)

I'm in San Angelo, about 3-4 hours away. Can you please tell me more about this?

Celtic Queen Explorer

This is my first gluten-free Thanksgiving but I'm pretty lucky. Our family always gets together on Friday for the holiday, instead of Thursday, so various family members can visit their in-laws on Thanksgiving Day. I usually end up cooking a dinner for my husband and son on Thursday anyway. This year it will be a gluten-free feast, so I'll just bring my gluten-free leftovers with me on Friday.

I guess I'm pretty lucky because my family and friends have been really supportive about the gluten free thing. My husband has been the least supportive (long story) but he's coming around. Plus I'm the one who does all the grocery shopping and cooking, so he has no choice but to eat gluten-free :lol:

Bobbie Jo Rookie

I'm sorry you have to go through that :(

I know exactly what you're going through. I've been gluten free for 2 years and I haven't had a Thanksgiving dinner with my family since. My sister and I don't get along at all, we don't speak and it goes beyond rivalry to a down right hatred. She uses the celiac to her advantage during the holidays. She opts to make the dinners for Easter and Thanksgiving, and makes nothing I can eat. I volunteer to make something and she gets angry and says it will taste gross and no one will eat it. I've spent my last 2 Thanksgivings and Easters alone because of her and her attitude towards me. It's not easy at all.

What is it with sisters? I had the same issue and I have decided not to be in the same room with her again. It means we will not see that part of the family on Thanksgiving, and my mom is so upset. But you know, that's okay. Peace is a good thing. We are actually going hiking instead on Thanksgiving and then over to some other relatives on the day after Thanksgiving for a gluten-free meal, since they are gluten-free too. You should read the book "Boundaries", and the section on famlies. Life is too short to put up with someone who hates you - even on Thanksgiving! (I know lots of people will not agree - but if you have someone attacking you in front of other relatives, then - it's best to avoid the whole situation). My mom and I are just getting together on days apart from holidays when my sister is there. Life is much more peaceful!!!

You are important rainer83!

catsmeow Contributor

I'm in San Angelo, about 3-4 hours away. Can you please tell me more about this?

The first time you come (Thanksgiving) you will be a guest. After that, you can join the group for $20 a year and receive news letters. We meet once a month and usually have a potluck, But Easter ans Thanksgiving are our big food fests.

Open Original Shared Link

I'll PM you the Facebook page. I'm not sure what links we can post here without the virtual hand slap.

bauerpratt Newbie

Nice to see I am not alone here!!! I was just diog. Celiac a few weeks ago and I am freaking out. We go to the in laws and it is full of gluten.

I dont want to be rude and ofcourse I want to eat, guess I could offer to make a fruit veggies tray.

jswog Contributor

The first time you come (Thanksgiving) you will be a guest. After that, you can join the group for $20 a year and receive news letters. We meet once a month and usually have a potluck, But Easter ans Thanksgiving are our big food fests.

Open Original Shared Link

I'll PM you the Facebook page. I'm not sure what links we can post here without the virtual hand slap.

Sounds great! IDK if we'd be able to make it or not, but I'd love to find a support group. I feel very alone out here in BFE stumbling in the dark!

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.