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

Job Interviews--How To Bring Up Celiac?


pinktulip103

Recommended Posts

pinktulip103 Newbie

Hello everyone! I was just diagnosed with celiac disease through a positive blood test and endoscopy two weeks ago. This forum has been so helpful! I am currently a graduate student studying biology and will be interviewing for postdoctoral positions this fall. Usually, for post-doc interviews, prospective employers will fly you out and you'll spend a few days meeting everyone in the lab and this always involves meals out at restaurants (basically EVERY meal is eaten out). At this point, I do not feel comfortable AT ALL eating anything prepared by someone other than myself. I have been eating entirely unprocessed foods and have already seen improvement in my migraines and BMs. Also, I will have no say in the restaurants and reservations will probably be made beforehand. I am already freaking out about how to handle this! When I am trying to set up interviews, should I bring up my celiac disease beforehand? I feel like it would be much better to tell them in advance versus them picking me up at the airport and taking me to dinner and saying "oh, by the way....I have celiac disease and can't eat...". But then again, I don't want to sound demanding in emails before I even show up to interview. I really don't feel like I should risk getting sick before I have to give a 1-2 hour job talk on my research! Also, when I go to these interviews, I will not have my own transportation and probably won't even know what hotel/where in town I am staying until I get there. What foods can I pack so that I don't starve for 2-3 days? I am thinking Quaker rice cakes, nut butters, Lara bars, homemade trail mix? I don't know if I will have access to a grocery store (depending where in town I stay), so anything that can't get on a plane with me may not be accessible. I am interested in labs at Northwestern, Harvard, and UCSF right now (atleast in big cities, so maybe I can take a taxi to the closest grocery store?) Usually these interviews are only 2 days, so I'm sure I can survive...but does anyone have any other ideas of food I can take with me? I am also a Type 1 diabetic and vegetarian. Has anyone else been through similar job interviews? I'm just worried because usually different people from the lab eat with the prospective post-doc candidate at each meal as a chance to get to know them and talk science/form opinions on their ability to fit in with everyone else in the lab. I just don't want to come across as snobby or anti-social. I will talk to my boss about this too beforehand to get his opinion (we have had a lot of post-doctoral candidates come through our lab) but I still haven't really had an opportunity to tell him that I have celiac disease.

Thanks,

Caroline


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



Celiac.com Sponsor (A8-M):



Ollie's Mom Apprentice

I don't know if this will be much help to you... but here goes anyway.

I have to travel occasionally for my job. While everyone else only takes carry-on luggage onto the plane, I have to pack a suitcase for all my food. ;) I bring gluten free "granola" bars, cereal, a few canned goods that I have found that don't upset me (and I bring a can opener and spoons!), nuts, ... you name it, I bring it. Sometimes I pack apples and oranges if I'm not crossing the border.

Some hotels are great with their breakfasts as they have actual fruit - not in a fruit salad, but the whole fruit - apples, oranges, bananas. In those cases I don't have to bring my own. Oh, also brining our own kettle and tea / coffee (if that's your kind of thing) is a must. Also, I always split my food between the carry-on and checked baggage so that I still have food in case they loose my bag.

As for eating at restaurants... the whole thing is scary. I tend to google my heart out prior to my trip to find gluten-free friendly restaurants in the neighbourhood I'll be in. In a pinch, I have had luck asking for a salad with no croutons and no dressing. Be prepared to send food back though! And to check it very carefully. Especially if the servers give you the dreaded 'blank stare' when you say you can't have gluten.

I would say not to say anything before your interview. Once there, if they say that they want to go for dinner, just mention that you have a gluten allergy (use the word allergy) and that you can't always eat at restaurants. Then try to guide them in the direction of a place that may be gluten-free friendly (ie - not a deli). If you've found a restaurant or two online that might work for you, you can always suggest one of those. You'd be surprised how accommodating people will be.

Absolute worst case, you go with them but don't actually eat anything. I've done that before too! I'm so used to being hungry now. ;)

Jenniferxgfx Contributor

Someone here suggested gopicnic mini meals. The hummus and cracker one is delicious!

I have done the grad school trip thing as a vegetarian and found it tough. As a gluten-free vegan, I think I'd send an email ahead of time to skip scheduling meals and ask for a different social activity (they're just trying to make sure youve got some social skills) like coffee or a walking tour of campus. All those places you mentioned should have nearby stores that'll sell gluten-free stuff. In SF, they're pretty gluten aware and even the corner stores have fresh local produce and Lara bars, generally.

Good luck finding a school! How exciting :)

chasbari Apprentice

Mat Lalonde is at Harvard. He is a monster intellect in the paleo world. He is good friends with Robb Wolf who is not only big on paleo but also has celiac. If you run across him he would understand where you are coming from. I would think that a biology department would be full of people able to understand the clinical implications of your situation.. Be genteel in your emails and you might not have the problems you are worried about. I think it's also a good idea to check with your current department head as you are planning as they should be able to give you great insight into how to handle the situation in a politically efficacious manner. May be a way to work in some education of others about celiac. (I know, probably not really the time nor place, though.) Best of skill in your upcoming interviews. Hope you get the best opportunity/situation.

CS

Juliebove Rising Star

Wow. I would think the diabetic and vegetarian part would be just as hard as the celiac in terms of packing food for a plane. I took my daughter to a dance convention and we had to pack food for three days. We didn't even fly and that was hard enough. We took canned beans but I don't think you could take those on a plane. I am also diabetic. Type 2 but I do use insulin. Do they have the "Just" products in your area? These are freeze dried veggies and fruit. I am not sure whether or not they make just peas. I think there are peas in their "Just Veggies" mix. I am trying to think of sources of protein. I sometimes eat the strawberries for snacks. Yes, they are a bit bulky in terms of size, but they are lightweight and dry.

I guess in terms of approaching these people about your diet you could probably just say that you need a place with a vegetarian and celiac menu. As a former vegetarian myself, I know that this in an of itself can make things a lot more difficult in dining out. If there is an Olive Garden or Old Spaghetti Factory in the areas where you'll be going, they do gluten-free vegetarian meals but they are pretty high in carbs. I think the pasta has something like 98g per plate. What I used to do when my daughter was younger was switch meals with her so I got the kid's portion. She is as tall as me now and soon to be 13 so that won't work any more.

pinktulip103 Newbie

Thanks for all of the replies! Really, the diabetic and vegetarianism is not an issue...I have been diabetic for almost 18 years and vegetarian for 14 years. I only mentioned it because I didn't want people suggesting I bring canned tuna or something! I can generally find something at any restaurant (even if it is just ordering a side salad and a baked potato)....but the new celiac diagnosis is what is really freaking me out. I really didn't think I had typical symptoms and when my endocrinologist suggested I may have celiac disease, I thought he was full of it. Then all my tests came back positive and after 2 weeks of being gluten-free, I have noticed a huge differenc in how I feel. I do think I accidentally ingested something last Friday, and my migraine STILL hasn't gone away. That is what really scares me. I always thought I was mostly asymptomatic until I realized what I was supposed to feel like (without gluten). I've read on here how symptoms can get worse after being gluten-free for periods of time, and don't want to get to the point where I can't even function if I get glutened (that would not make my job talk go very well!). I have always felt bad for people going out of their way to accomodate me and having celiac requires even more accomodations. I think telling them beforehand is probably best but doing it in the most tactful way possible and making sure they are already discussing arrangements for me to visit. If anyone has any other suggestions for things to bring, I would really appreciate it! Thanks!

Skylark Collaborator

Wow, they feed you for 2-3 days on a postdoc interview??? I got lunch and dinner on one day and that was it.

On job interviews, I explain that I have celiac disease, research the area, and make specific suggestions about restaurants that can accommodate me. For packing, I can survive pretty well on a loaf of Udi's and peanut butter. Unfortunately, TSA frowns on peanut butter unless you check it. You can have the usual 3.4 oz in your quart baggie but that's all.

Open Original Shared Link

San Francisco should be pretty celiac-friendly. I had a very easy time traveling there. Yes, you should be able to cab to a 7-11 if not a grocery store. I've found bananas, nuts, yogurt, and lunch meat to eat at 7-11 and I'm good to go with a loaf of Udi's.


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



Celiac.com Sponsor (A8-M):



annegirl Explorer

Just fyi - check out the natural peanut butter section of your store. I found little packets of peanut butter, almond butter, and honey almond butter. I packed those in my suitcase in a plastic baggie with a bag of apples, oranges and a ton of other stuff and they didn't even blink.

Lara bars, nuts, fruit and veggies all travel well. I've found that as I get used to my diet it gets much easier to dine out. Not that I still don't have panic attacks about it....but it's much easier. I have to travel quite a bit for work and have made out fine without getting sick. I do tend to lose weight while traveling now, but to me that's a bit of a bonus round.

RL2011 Rookie

Aside from the food issues you will encounter, when you speak of your condition, turn your celiac disease into an asset of sorts. Speak in terms of it providing you with more passion for research even when the research you are doing may not directly impact you. Explain it as a source to boost your empathy when undertaking research in general as you can relate to people's problems.

Just a thought... Wish you the best of luck in your future!

tea-and-crumpets Explorer

There is a wheat-free bakery/restaurant in Evanston, near Northwestern, called Rose's. Maybe that would be an option when you're there? It's not fancy, but the food is good.

loneferret Newbie

You know during an interview at some point they usually say "Do you have any questions?" I would mention your condition then. No safer time seeing the floor is open to you...

seezee Explorer

I live in Cambridge and work for Harvard and there are lots of places you can buy food, Shaws in Porter square has a gluten-free section lots of prepared gluten-free frozen/canned foods and is on the red line. (there's another Shaws on Beacon street which has nothing gluten-free though so go to the Porter Square one)

There are also 3 or 4 whole foods markets in Cambridge which all have a big supply. There is a gluten-free bakery called Glutenus Minimus and they supply several of the local pizza place and cafes between Harvard Square and Porter on Mass Ave. (Cafe Zing in Porter Square books, Simons coffee shop, and Stonehearth Pizza) with gluten-free pizza crusts and pastries. Close to campus you can eat at Legal Seafoods in Harvard Square. They have a celiac menu and we've not had problems. We also often eat at Tamarind House which is a Thai restaurant between Harvard and Porter Square. They don't have a gluten-free menu per se but are very nice and my daughter and nephew have always been OK there. You just have to tell them that you can't eat any wheat or gluten and they'll make it w/out any soy sauce. They have good tofu dishes. Bertucci's has a gluten-free menu, but we haven't tried it as it's mostly grilled meat and salads. I think if you look on yelp.com for gluten free you'll find other places. Since my daughter is 12, we don't tend to go to the fancier places. Stonehearth pizza has a gluten-free menu but they are super slow and the staff has made some mistakes, so be wary of that one.

I also suggest you speak to the admin at Harvard who is setting up your travel and let him/her know about your dietary/medical issues. Please think that if they are inviting you to interview they will want to impress you as well and no one would want to take you to eat somewhere and make you ill. Whoever is setting up the travel can be sure to put you in lodging with at least a fridge and microwave oven. There are lots of B&B kind of places that are more like an in-law apartment with a kitchenette.

The biology dept. is in Cambridge right (not at Harvard medical school).

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,556
    • Most Online (within 30 mins)
      7,748

    Rachel Wilson
    Newest Member
    Rachel Wilson
    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.