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

catsmeow Contributor

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!

Aw, that's to bad. You actually do have a support group in San Angelo, but they don't have a website. Let me see if I can find it again. BME....ha ha..I have not heard that term in a long time. Funny!!!

Celiac Sprue Association

CSA Resource Unit #3023

Becky Zarnowski, San Angelo

325-944-0130, bazarnow@suddenlink.net


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



Celiac.com Sponsor (A8-M):



jswog Contributor

Aw, that's to bad. You actually do have a support group in San Angelo, but they don't have a website. Let me see if I can find it again. BME....ha ha..I have not heard that term in a long time. Funny!!!

Celiac Sprue Association

CSA Resource Unit #3023

Becky Zarnowski, San Angelo

325-944-0130, bazarnow@suddenlink.net

Thank you, Trish! I'm going to call her!

MenHen Rookie

Hello! I am new to the board and only about 4 weeks gluten free, so I understand the stress of the holidays. What has helped me is pre-planning. Are your daughters gluten free for health reasons or out of convenience? If they cannot eat gluten, I would highly suggest you cooking your own meal for everyone either before Thanksgiving, as the others have mentioned, or staying home on Thanksgiving day and cooking then. That way you and your daughters get to have a full spread. Then either bring leftovers to your family or spend the next day or weekend with them. Whichever you feel you can do best.

Even though my dad and step-mom are supportive, there is no way I would trust her to cook gluten free on a holiday, which we have a larger family. Maybe after she continues to learn, but there are just too many people grabbing this or that. It would just be asking way too much of her as well. Fortunately for me, my two sisters and I have already cooked a full t-day dinner for my mom and grandma for the past several years. We have it before T-day or early T-day. They are both in a nursing home and unable to travel the distance to our homes. This year, I just told my step-mom to not be concerned about the gluten, that I would bring left overs from my mom's dinner. Also, I had told her before my first visit (before I even knew her attitude about it) that if I turn something down to eat, its not that I am being rude. Its because I dont want to get sick. Its not worth it. If your parents are not supportive at all then it will be tougher. This will be for the rest of your life, so try to think of how you want this to go now and in the future. Be polite, but firm. I know it would be awesome for them to cook gluten-free, but that is obviously not going to happen, at least anytime soon.

I think by being pro-active before people give you a chance to be unsupportive has helped me. When I go to family or friends, I tell them that, sadly, I won't be able to eat what they serve and give a brief reason as to why. I ask what they plan to serve, so I can bring similar food. I think that takes the burden off of others too. I know that a good friend that is a very patient and understanding person freaked out the first time I came over. He didnt want to make any mistakes or make me feel uncomfortable. It made me realize how stressful it can be on others as well as us.

Anyway, I made my first gluten free dressing this weekend and it turned out great. My mother's recipe is gluten free except the bread. I just subbed gluten-free bread for regular bread and it was great. There are lots of recipes out there. I plan to make green bean casserole this weekend. I googled a recipe and found one that had instructions for making your own french fried onions. Personally for me, dressing, turkey, green bean casserole and my pecan pie are all I care about. I plan to get fresh pecans this year for Thanksgiving and Christmas. Although frustrating, start planning now and it will make you feel a lot better!

bartfull Rising Star

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!

I have a sister like that too! As a matter of fact, she "disowned" the whole family, and now she is my only living relative, but I haven't talked to her in almost eight years. She lives in another state. When I moved here (South Dakota) from Connecticut I thought I should call her to let her know, just in case she ever needed to talk to me. She said she doesn't even want to know me. Well, OK I guess.

I must admit though, after reading some of these posts, it's not too bad being "alone in the world". I can get together with friends on the holidays or I can just stay home. Lately, I and some other single friends who don't have family here have been going to the American Legion, which puts on a FABULOUS meal. I will be bringing my bowl of brown rice with caluiflower and chicken, and eating it at the Legion with my friends.

rainer83 Newbie

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!

Thank you! I'm so relieved to know that I am not alone. People always judge my situation by saying "You can't hate your sister, she's family!" Well, family doesn't treat each other like our sisters do. I usually make a small desert for my parents and I when I come down, and we have that as a family. She's even got her kids against the gluten free life. Every time I make something for Christmas, she tells them not to eat it or they'll get really sick. You're right, life is too short to put up with people like them, which is why I don't. She ruined my life thus far and I'll be damned if I keep letting her ruin Thanksgiving, Christmas and Easter!

alex11602 Collaborator

I talked to my mom yesterday and she said that she was going to make the stuffing gluten free and would make baked apples for dessert for my family. I was extremely shocked because she has always made the same foods from the same recipes and I am so grateful. I still say that the holidays are a bit trying though.

Katrala Contributor

I just sat down with my cousins this morning to plan our family Thanksgiving.

I'm fortunate, though, in that my family is very supportive and one of my cousins is a manager at a Whole Foods.

We are having some stuff that has gluten and some stuff that isn't. We always have several people bringing stuff and I'm bringing several gluten-free dishes and a gluten-free dessert.

The night before I always have a smaller Thanksgiving at my mom's (we all go to the bigger Thanksgiving the next day) and she is making sure the turkey she makes isn't CCd, so I'm just going to bring some of that with me the next day so I can have turkey as well.

While I know every family isn't like mine, I've found that when dealing with people who just don't get it the best thing is speak up and offer to bring whatever, etc.

Or, if your family is the type that really wants everything to be just-so and perfect, bring peanut butter sandwiches to eat for yourself and mess up the scene. :D


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



Celiac.com Sponsor (A8-M):



  • 2 weeks later...
Bobbie Jo Rookie

Thank you! I'm so relieved to know that I am not alone. People always judge my situation by saying "You can't hate your sister, she's family!" Well, family doesn't treat each other like our sisters do. I usually make a small desert for my parents and I when I come down, and we have that as a family. She's even got her kids against the gluten free life. Every time I make something for Christmas, she tells them not to eat it or they'll get really sick. You're right, life is too short to put up with people like them, which is why I don't. She ruined my life thus far and I'll be damned if I keep letting her ruin Thanksgiving, Christmas and Easter!

Amen sister.

tarnalberry Community Regular

Either make the things you usually have gluten free at home and bring food for yourself, eat before hand, or invite people over and make it all gluten-free. Traditions have to change eventually, and all of it can be gluten free, likely without anyone knowing.

katecopsey Newbie

Not sure that this is going to help you but first of all take a good snack with you so that if you have to sit at the table, you can pick at the food only. Turkey without gravy should be ok, so should mashed potatoes unless they come from a packet (which I have idea if they are gluten-free). Some turkeys can be infused with 'stock/moisturizers' or something but not all of them. How does she make the bean salad? could you make that using gluten-free ingredients?

Of course your husband (and I love that he is supportive - that is so helpful) should tell the family that anything with ingredients that contain flour are not acceptable for you and make you very ill. Being able to be social and with family is important, and the meal is only part of the gathering, so try to be a little more positive and go for the people, and take a few dishes that you make to share.

Good luck!

domesticactivist Collaborator

I think the way you are feeling is a normal part of adjusting to your new life. In a way it is a grieving process. Let yourself have those feelings.

On the practical side, we bring our entire meal for our family, and a dish to share. This way cross contamination and our other dietary details don't ruin the holiday. This year we are bringing a turkey, stuffing, cranberry sauce, veggies of some sort, and squash pie for our family. We are also bringing a green salad to share. It is kind of weird and really is a lot of work, but the family is getting used to us bringing our own food now and it is worth it to us to be able to be there.

cap6 Enthusiast

I'm not looking forward to the holiday. T'giving will only be the 3 of us but this is the time when my 98% gluten free household decides that they need gluten bread for turkey sandwiches, gluten stuffing, gluten muffins, gluten pie . "It's not Thanksgiving without it". grrr :angry:

mommida Enthusiast

Thank you! I'm so relieved to know that I am not alone. People always judge my situation by saying "You can't hate your sister, she's family!" Well, family doesn't treat each other like our sisters do. I usually make a small desert for my parents and I when I come down, and we have that as a family. She's even got her kids against the gluten free life. Every time I make something for Christmas, she tells them not to eat it or they'll get really sick. You're right, life is too short to put up with people like them, which is why I don't. She ruined my life thus far and I'll be damned if I keep letting her ruin Thanksgiving, Christmas and Easter!

So what would she do if she or her kids ended up having Celiac!!!? :unsure:

In life you get to choose your friends.

I'm bringing gluten free safe food to the in-laws for dinner. I should have everything ready for a quick zap in the micro.

For Christmas we stay home and invite famnily over for a fully gluten free meal. My sister comes early to use gluten free flour for her recipes. We have extra time to visit and I know she's my friend too.

When we learn how to give up toxic gluten, we sometimes have a harder time giving up the toxic relationships. ;)

Happy Thanksgiving to all my gluten free Peeps (sorry I'm late for you Canadians)! Celebrate any way you feel is best for you! :)

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.