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

Spending the Holidays at someone else's House


Bumpeh

Recommended Posts

Bumpeh Newbie

Hello everyone, I'm somewhat new to these forums and I could use some help/advice. This Christmas I will probably be heading up North to Virginia to spend Christmas/New Years with someone important. He nor his family eat gluten free, and I unfortunately have celiac disease.

How can I cope while I'm living with them? What can I eat, how should I eat, will I have to prepare every meal I eat by myself? I'm sure we've all felt that we've never wanted to inconvenience anyone, but it is a disease with painful consequences. I remember once turning down gluten-free brownies because the person who made them(specifically for me) made them in a gluten kitchen which probably resulted in cross contamination.

So, does anyone have any helpful tips/advice/ideas that can help me through this holiday season? Thanks guys!


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master

Make your own versions of what they are having, freeze/vacuum bag your portions. Take these and inform them it is not intended as a offense but due to your disease you have to do this. Reheat your meals and eat on paper plates with disposable utensils. This way you can have the family experience and eat together with less chance of getting sick. Alternatively you can bring and eat meal replacement shakes during yout stay.

cyclinglady Grand Master

Well, the bottom line is that YOUR health comes first.  Eat only the food you prepared or oversaw --  period.  

Are you flying or driving?  If driving, pack a cooler with lots of prepaid meals, snacks.  Plan on shopping at the local grocery store.  Search through "Find Me Gluten Free" for the area (I just did this last night for our upcoming vacation).  Make sure the reviews are written by celiacs.  (Luckily, I found several 100% gluten free restaurants and one that has a dedicated cooking area and who's Mom has celiac disease).  

Eat off your host's plates and use their silverware if they have a dishwasher.  If not, purchase some plastic and paperware.  Stick a pot from home in your luggage and a few utensils.  Use foil or parchment paper as a barrier.  I use paper plates for cutting veggies.

I visit my relatives and stay in their homes.  At my parents, I keep a bin of gluten-free cookware, etc.) at their house.  I oversee my Mom cooking gluten-free safe food.  I do not trust her completely because she does not have to be careful 24/7 like me.  

Will be traveling this Fall with another couple.  There will be just some meals that I will be eating out in the car or in my hotel room.  For me, a glutening can impact me for three months (as measured by celiac antibodies by my GI), so taking chances is not worth it.  

Will I have fun?  Plan on shopping, hiking, bike riding, tennis and relaxing by the pool.  Isn't that what it is all about?  

I get it.  These friends are now used to my ways.  They never push me into anything.  My relatives get it, but it took a while.  I was persistent.  I often dine out and just order a drink.  There's no reason to miss out on the fun of socializing.

Take the time to talk to your hosts and explain.  Maybe bring a printout.  Talk to your boyfriend and figure out what's going to work with his parents.  Bring or purchase some gluten-free goodies that can be shared (just be in line first at the buffet).  

I hang at my parent's lake house with 20 or more gluten eaters.  I oversee food prep, use my own stuff and hubby and I eat first.  We stash our food away from the crowd.  We have never been glutened ever.  Wash up before you eat and you'll be fine.  

It's work, but in the end you'll be happy and will not have to worry!  

Enjoy! 

  • 3 weeks later...
Nikki2777 Community Regular

I go to  my inlaws every year for the holiday.  They love to cook and they're very conscientious at this point about my issues, but I generally bring up my own breakfast cereal and gluten free bread (and some wine!).  When I'm up there, I head to the grocery store and get some packaged cold cuts so I can make myself a sandwich when I need to, some yogurt and gluten free pretzels to munch on when everyone else is snacking.  When they make eggs, I wash out the skillet beforehand and ask that they use a fresh bar of butter to grease the pan.  I agree on the foil or parchment.  But basically, I don't try to replicate their meals - it's too much work and makes them self-conscious.  I just opt out of what they're having and fix myself a sandwich.  It's 5 days of inconvenience, but it's ok.

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. - knitty kitty replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Son's legs shaking

    2. - lizzie42 replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Son's legs shaking

    3. - knitty kitty replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Son's legs shaking

    4. - lizzie42 replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      6

      Son's legs shaking

    5. - Scott Adams replied to Russ H's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Anti-endomysial Antibody (EMA) Testing

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,870
    • Most Online (within 30 mins)
      7,748

    KABoston
    Newest Member
    KABoston
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • knitty kitty
      Blood tests for thiamine are unreliable.  The nutrients from your food get absorbed into the bloodstream and travel around the body.  So, a steak dinner can falsely raise thiamine blood levels in the following days.  Besides, thiamine is utilized inside cells where stores of thiamine are impossible to measure. A better test to ask for is the Erythrocyte Transketolace Activity test.  But even that test has been questioned as to accuracy.  It is expensive and takes time to do.   Because of the discrepancies with thiamine tests and urgency with correcting thiamine deficiency, the World Health Organization recommends giving thiamine for several weeks and looking for health improvement.  Thiamine is water soluble, safe and nontoxic even in high doses.   Many doctors are not given sufficient education in nutrition and deficiency symptoms, and may not be familiar with how often they occur in Celiac disease.  B12 and Vitamin D can be stored for as long as a year in the liver, so not having deficiencies in these two vitamins is not a good indicator of the status of the other seven water soluble B vitamins.  It is possible to have deficiency symptoms BEFORE there's changes in the blood levels.   Ask your doctor about Benfotiamine, a form of thiamine that is better absorbed than Thiamine Mononitrate.  Thiamine Mononitrate is used in many vitamins because it is shelf-stable, a form of thiamine that won't break down sitting around on a store shelf.  This form is difficult for the body to turn into a usable form.  Only thirty percent is absorbed in the intestine, and less is actually used.   Thiamine interacts with all of the other B vitamins, so they should all be supplemented together.  Magnesium is needed to make life sustaining enzymes with thiamine, so a magnesium supplement should be added if magnesium levels are low.   Thiamine is water soluble, safe and nontoxic even in high doses.  There's no harm in trying.
    • lizzie42
      Neither of them were anemic 6 months after the Celiac diagnosis. His other vitamin levels (d, B12) were never low. My daughters levels were normal after the first 6 months. Is the thiamine test just called thiamine? 
    • knitty kitty
      Yes, I do think they need a Thiamine supplement at least. Especially since they eat red meat only occasionally. Most fruits and vegetables are not good sources of Thiamine.  Legumes (beans) do contain thiamine.  Fruits and veggies do have some of the other B vitamins, but thiamine B 1 and  Cobalamine B12 are mostly found in meats.  Meat, especially organ meats like liver, are the best sources of Thiamine, B12, and the six other B vitamins and important minerals like iron.   Thiamine has antibacterial and antiviral properties.  Thiamine is important to our immune systems.  We need more thiamine when we're physically ill or injured, when we're under stress emotionally, and when we exercise, especially outside in hot weather.  We need thiamine and other B vitamins like Niacin B 3 to keep our gastrointestinal tract healthy.  We can't store thiamine for very long.  We can get low in thiamine within three days.  Symptoms can appear suddenly when a high carbohydrate diet is consumed.  (Rice and beans are high in carbohydrates.)  A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function, so symptoms can wax and wane depending on what one eats.  The earliest symptoms like fatigue and anxiety are easily contributed to other things or life events and dismissed.   Correcting nutritional deficiencies needs to be done quickly, especially in children, so their growth isn't stunted.  Nutritional deficiencies can affect intelligence.  Vitamin D deficiency can cause short stature and poor bone formation.   Is your son taking anything for the anemia?  Is the anemia caused by B12 or iron deficiency?  
    • lizzie42
      Thank you! That's helpful. My kids eat very little processed food. Tons of fruit, vegetables, cheese, eggs and occasional red meat. We do a lot of rice and bean bowls, stir fry, etc.  Do you think with all the fruits and vegetables they need a vitamin supplement? I feel like their diet is pretty healthy and balanced with very limited processed food. The only processed food they eat regularly is a bowl of Cheerios here and there.  Could shaking legs be a symptom of just a one-time gluten exposure? I guess there's no way to know for sure if they're getting absolutely zero exposure because they do go to school a couple times a week. We do homeschool but my son does a shared school 2x a week and my daughter does a morning Pre-K 3 x a week.  At home our entire house is strictly gluten free and it is extremely rare for us to eat out. If we eat at someone else's house I usually just bring their food. When we have play dates we bring all the snacks, etc. I try to be really careful since they're still growing. They also, of course, catch kids viruses all the time so I  want to make sure I know whether they're just sick or they've had gluten. It can be pretty confusing when they're pretty young to even be explaining their symptoms! 
    • Scott Adams
      That is interesting, and it's the first time I heard about the umbilical cord beings used for that test. Thanks for sharing!
×
×
  • 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.