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

Traveling For Business To Seattle/bellevue (Suggestions)--Newly Diagnosed


alannakitty

Recommended Posts

alannakitty Newbie

Hi everyone!

 

I just joined.  I'm in the process of being diagnosed and after my last test I will be on the gluten-free diet/lifestyle. 

 

My question or my appeal for advice is that I will be traveling for business not even a month into my new lifestyle change and I'm afraid that going away on business will make what is already a hard task (finding things to eat that are safe/allowed) will be even harder.

 

Does anyone have any suggestions for flying/traveling gluten free?  I figured I can bring some snacks for the plane they are offering food service.  I also notified the hosts of the conference and they are aware of my special dietary needs for the few meals they will be providing. 

 

What do people suggest?  I just read that carrying a card with what I'm "allergic" to is helpful (different forum).  I feel like when I ask people about food prep and other things they look at me like I've grown two heads even if they are like ... ah, yeah gluten free. 

 

Thanks in advance!

  • 2 weeks later...

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



Celiac.com Sponsor (A8-M):



ryann14 Rookie

Ask questions, talk to managers, if you have a smart phone or use of a computer use the application or website find me gluten free. I don't live in Washington but when I do travel then I bring snacks and go to to the grocery store and buy food I can make in the hotel. Good luck! :)

MinnesotaCeliac Rookie

Hi everyone!

 

I just joined.  I'm in the process of being diagnosed and after my last test I will be on the gluten-free diet/lifestyle. 

 

My question or my appeal for advice is that I will be traveling for business not even a month into my new lifestyle change and I'm afraid that going away on business will make what is already a hard task (finding things to eat that are safe/allowed) will be even harder.

 

Does anyone have any suggestions for flying/traveling gluten free?  I figured I can bring some snacks for the plane they are offering food service.  I also notified the hosts of the conference and they are aware of my special dietary needs for the few meals they will be providing. 

 

What do people suggest?  I just read that carrying a card with what I'm "allergic" to is helpful (different forum).  I feel like when I ask people about food prep and other things they look at me like I've grown two heads even if they are like ... ah, yeah gluten free. 

 

Thanks in advance!

No need to worry if you are prepared, it takes some planning and knowledge (comes with time and experience) as it will not be as easy as before going gluten free. It also depends on your comfort level of eating out. When I travel I carry safe gluten free food with me on my carry on (Laura bars, almonds...etc and twice as much as I'll need just in case there is a delay). I will book hotels that I will have access to a microwave and fridge (either a room with a kitchenette or a hotel that will deliver a small fridge and microwave to the room). I look for a wholefoods (usually book a hotel near one) and swing by a get food for my stay.  Note: you can find gluten-free food at almost all stores now (not a huge variety,but it is getting better)...I just prefer wholefoods.

 

Another very helpful thing to do is contact the local GIG/Celiac support group prior to going, so you are armed with information from people that know the gluten free diet and the local area. Most if not all are more than willing to help a fellow Celiac/GInC. Awesome folks.

 

Contact me if you ever travel to the Twin Cities and I'll give you a list places to eat and where to get gluten-free food.

 

Cheers and goodluck!

cyclinglady Grand Master

All excellent suggestions!  I would just add that if your hotel offers a buffet type breakfast, talk to the people who actually prepares your food.  More than likely, they'll accommodate you. Lots of them use prepackaged foods and will even show you the box.  Other's will cook your eggs on a separate grille.  For business we (both hubby and I are gluten-free) book rooms with refrigerators and we grocery shop upon arrival.  Google for gluten-free restaurants in advance.  

tarnalberry Community Regular

How long is your flight? Where are you staying? I live immediately south of Bellevue (as in, the city border is across the street), and there is a lot of gluten-free friendly stuff in the area. (More in Seattle, but you didn't specify where you are staying...)

  • 1 month later...
notme45 Newbie

Here is my advice:

 

1.  Get the "Find Me gluten-free" app for your smartphone.  If you don't have a smartphone then buy a smart phone.  The app will help you find gluten free restaurants and grocery stores that sell gluten free products.  I will make a big difference in your life when you travel.

 

2.  Plan in advance where you will buy food at and bring food with you.  On my last trip I had a frozen loaf of bread in my luggage (I like Canyon Bakehouse bread) and when I landed I went to a deli and bought lunch meat.  Lunch meat is almost always gluten free. 

 

3.  In general, the nicer the restaurant is the more accomodating they will be. 

 

4.  If you are going to a restaurant, try to call in advance and ask questions. 

 

5.  Your best bet is usually to order a steak with NO seasonings other than salt and pepper and no sauce.  Other good option is roasted chicken.   

 

6.  GoPicnic is a brand of boxed snacks that requires no refrigeration. You can buy these at Target, Amazon, or Sprouts (if you have Sprouts near you).  GoPicnic is good for plane rides and as an emergency meal. 

 

7.  Subscribe to Gluten Free Living

 

8.  Traveling with Celiac Disease is a bit of a pain but is not the end of the world as long as you plan ahead.

  • 2 months later...
Tim-n-VA Contributor

I will have a lengthy layover at the Seattle airport in late October.  Allowing for a comfortable cushion on travel by the light rail, I could have 3-4 hours.  Any suggestions for lunch in the downtown area?


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



Celiac.com Sponsor (A8-M):



Jestgar Rising Star

What do you like to eat?

 

Open Original Shared Link in the ID is awesome.

 

Open Original Shared Link is good.  Really good if you hit happy hour

 

Most places are really aware of what they serve and I've never had a problem.

Tim-n-VA Contributor

Moderately adventurous: Something either uniquely Pacific NW or something not readily available gluten free. For the latter, I saw "biscuit b%$@#" online.

Jestgar Rising Star

If you are traveling with someone else, the Open Original Shared Linkis fun.  You get a pile of steamed seafood, corn and potatoes dumped on your table.  Just ask them to skip the bread that comes with the meal.

Salax Contributor

There is a PF Changs downtown, a place (I think it's called something cinnamon?) in pike's that has amazing baked goodies (if they are still there, been awhile since I was there in 2011), try the gluten free registry website, found most places on that site. :)

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,551
    • Most Online (within 30 mins)
      7,748

    Newest Member

    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

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • 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.