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

How To Explain That I Don't Want To Eat Out


llama3

Recommended Posts

llama3 Apprentice

I have relatives who want to take me out to restaurants and I find it so stressful right now that it's just not worth it, but I don't know how to explain that to them. When I go out, my choice seems to be between pain/discomfort or eating a very expensive plate of lettuce. Either way, there is lots of stress and I feel embarrassed asking the waiter to leave off ... everything. I just don't want to do it.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

There is nothing wrong with explaining to them that you are having a difficult time figuring out what you can and can't eat at the moment, and that adding in the complexity of a restaurant menu is just too stressful for you right now. Just thank them and tell them you will take up their offer when you feel more comfortable doing so. I presume you have mentioned that you are celiac/gluten intolerant??

srall Contributor

I have BTDT. I was just done with it when I spent $25 on a plain caesar salad...just lettuce and plain chicken...and oil. Ugh.

So, I'm married and my husband is on board since I do all the cooking, but for the times it does come up, I usually eat before I go, then order a glass of wine. The one piece of advice I do have is to try and make sure you find a way to be social. I'm almost 2 years in with myself and my 8 year old and I'm noticing invitations (especially for my daughter) dropping off. I'm struggling with trying to find ways to make my diet and my daughter's very easy on others. I should add that I do send food with my daughter, so I'm not expecting anybody else to make allowances for her.

I don't really know the answer to this problem...host people at your house with safe foods? Arrange with restaurants to see if you can bring your own plate? Just order coffee or a drink? It's something we are still trying to figure out.

llama3 Apprentice

I presume you have mentioned that you are celiac/gluten intolerant??

Yes, but at this point I'm tentatively self-diagnosed so it's hard to be taken seriously. I will try to explain it though as you said.

I have BTDT. I was just done with it when I spent $25 on a plain caesar salad...just lettuce and plain chicken...and oil. Ugh.

Exactly! I'm also avoiding dairy and I know I cannot tolerate onions and am allergic to chilies. Potatoes also seem to be a problem. I find plenty of foods to eat at home but when I go out it seems as if restaurants ONLY know how to cook with the foods I can't eat.

Juliebove Rising Star

Just tell them there is nothing safe for you to eat there. Do you have any restaurants in your area with a gluten-free menu? We do have some here.

You could also try to find places that cook from scratch and get to know the chefs and/or owners. That's what we do. They will gladly cook special foods for us. Look for places that mention food allergies on the menu.

But really in the beginning it is probably best just to cook the food yourself. That way you know it is safe.

Chad Sines Rising Star

I have the same problem. My parents like to eat out at sit down places but often I just want to eat at home or grab some take out. I think it is from a pattern of bad dining experiences where I have gotten sick before even finishing the meal. At least at home if it happens, I am in a "safe" place so to speak.

domesticactivist Collaborator

Have you tried suggesting alternatives? What are the motives behind going out? Could it be they think it will be easier because everyone can have their own plate? Does noone have the space to host? Is it just what they are used to?

I have a couple blog posts that might help you:

The holidays

Going out to eat

Crazy diet people 1 2 and 3

They are on the site linked from my profile.

Basically, it makes sense not to want to go out to eat. If your family members can not accept that, when you have gently explained and offered alternatives, there is not much to be done but accept that limitation of the relationship.


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



Celiac.com Sponsor (A8-M):



llama3 Apprentice

Have you tried suggesting alternatives? What are the motives behind going out? Could it be they think it will be easier because everyone can have their own plate? Does noone have the space to host? Is it just what they are used to?

I have a couple blog posts that might help you:

The holidays

Going out to eat

Crazy diet people 1 2 and 3

They are on the site linked from my profile.

Basically, it makes sense not to want to go out to eat. If your family members can not accept that, when you have gently explained and offered alternatives, there is not much to be done but accept that limitation of the relationship.

It's more that it's just what they're used to and it's something nice that they can do for me. If I cook for them or go out but don't eat anything, then they don't feel as if they are giving me anything anymore - even though I would rather just have their company.

Thanks for directing me to your blog, it looks good.

kareng Grand Master

It's more that it's just what they're used to and it's something nice that they can do for me. If I cook for them or go out but don't eat anything, then they don't feel as if they are giving me anything anymore - even though I would rather just have their company.

Thanks for directing me to your blog, it looks good.

Maybe they could buy steaks or an expensive fish and cook with you? Buying the food that's niceer than usual might make them feel they are treating you.

Skylark Collaborator

There aren't any restaurants that work for you? I'm pretty happy at Outback with an unseasoned steak, salad, and steamed veggies. It's not super-expensive.

domesticactivist Collaborator

I really like kareng's idea. ps, thanks for checking out my blog (oh, and I just added pictures from this Thanksgiving to the Holidays post).

Since you know your relatives just want to do something nice for you, even though it's awkward you probably just need to tell them what you would appreciate more. They love you and will adjust.

Elizabeth5220 Apprentice

I'm having the same problem...and I'm from a small town and we don't have Outback, PF Chang's, Chili's, etc!! I'd have to drive 75 miles one way to find a good gluten-free restaurant... :angry::angry:

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      14

      Ibuprofen

    2. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      My only proof

    3. - Scott Adams replied to wellthatsfun's topic in Coping with Celiac Disease
      1

      still struggling with cravings

    4. - Scott Adams replied to Colleen H's topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Oh my goodness medication causing pain !!!!

    5. - Scott Adams replied to Me,Sue's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      Knowing what to do when feeling unwell.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,871
    • Most Online (within 30 mins)
      7,748

    GR82BNTX
    Newest Member
    GR82BNTX
    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

    • cristiana
      Hi Colleen Are you supplementing B12/having injections? I have learned recently that sometimes when you start addressing a B12 deficiency, it can temporarily make your symptoms worse.  But it is important not to stop the treatment.  Regarding your problems with anxiety, again that is another symptom of a B12 deficiency.   I didn't know what anxiety was until it hit me like a train several months before gastrointestinal issues began, so I can certainly relate.   Two books which helped me hugely were At Last A Life by Paul David (there is a website you can look up) and The Depression Cure: The Six-Step Programme to Beat Depression Without Drugs by Dr Steve Llardi.  Although his book is aimed at people who have depression, following the principals he sets out was so helpful in lessening my anxiety.  Llardi suggests we need to focus on getting enough: - physical exercise - omega-3 fatty acids - natural sunlight exposure - restorative sleep - social connectedness - meaningful, engaging activity   ... and we should feel a lot better. That is not to stay you must stop taking medication for depression or anxiety if you have been prescribed it, but adopting the changes Dr Llardi sets out in the book should really help. Can I just ask two more questions:  1) you say that you are B12 deficient, did they test your iron levels too?  If not, you really ought to be checked for deficiency and, 2) did they check your thyroid function, as an overactive thyroid can be cause rapid heartbeat and a lot of coeliacs have thyroid issues? Cristiana        
    • Jmartes71
      Hello still dancing around my celiac disease and not getting medically backed up considering Ive been glutenfree since 1994.All my ailments are the core issue of my ghost disease aka celiac disease. Im angery because the "celiac specialist " basically lightly dismissed me.Im extremely angery and fighting for a new primary care physician which is hard to do in Northern Cali.So currently without and looking.Im angery that its lightly taken when its extremely serious to the one who has it.My only evidence is a brochure back in the days when I got news letters when I lived at my parents.It was published in 1998.I was diagnosed before any foods eliminated from my diet. Angery doctors don't take seriously when Im clearly speaking.I did write to the medicine of congress and have case number.
    • Scott Adams
      I totally get this. It's absolutely a grieving process, and it's okay to feel gutted about the loss of those simple joys, especially at 18. Your feelings are completely valid—it's not about being ungrateful for your amazing boyfriend, it's about mourning the life you thought you'd have. That "tortured by the smell" feeling is so real. It does get easier, I promise, but it's okay to sit in the sadness and just vent about how much it stings right now. Thanks for sharing that. Celiac.com has published a book on our site by Jean Duane PhD called Gluten-Centric Culture, which covers many of the social aspects of having celiac disease: This chapter in particular covers issues around eating with family and others - Gluten-Centric Culture: Chapter 5 - Grabbing A Bite Together:    
    • Scott Adams
      Many of us with celiac find that the fillers in medications can cause a reaction, and sometimes our bodies just process things weirdly. That "rebound muscle pain" and "burning feet" you described sounds awful and is a huge red flag. It's frustrating enough managing the diet without medication causing setbacks. So sorry you're dealing with this, but you're definitely on the right track by connecting the dots. You can search this site for 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
      It's so tough when you're doing everything right and still get hit with it. I'm glad you're figuring out a system that works for you—the peppermint tea and rehydration powders are smart moves. It sounds like you've really learned to listen to your body, and that's half the battle. Sticking to simple, safe food at home is the best way to build yourself back up. It's great you can take the time to rest properly. Thanks for sharing what works; it's a big help to others figuring this out too. This article, and the comments below it, may be helpful:    
×
×
  • 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.