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

New Diagnosis, Quick Question


Z3ro

Recommended Posts

Z3ro Newbie

I've just been diagnosised with Celiac and have been eating gluten free for the past week.  Going ok so far, but I have a question about a scenario that I'm sure will come up.

 

In the course of my reading up on the disease, I've read in many places that any gluten is bad; a quote I've read several times is that one crumb is the same as eating a loaf of bread.  I understand (mostly) the autoimmune response and the fact that it attacks your small intestine even if you have no external symptoms.

 

But what happens when you're in a situation that eating gluten becomes unavoidable?  Specifically, something like a family party, where I can bring my own food and insult the host, or be almost assured of being CCed.  Even if there are gluten free options (say, turkey, fresh veggies, etc), they've been prepared in the same kitchen as all the gluten products by someone who does't understand CC the way I do.

 

Given this situation, where I'm almost assuredly eating some amount of gluten, should I just go whole-hog?  If a crumb is the same as a loaf of bread, why not just eat the bread, assuming I can handle the external symptoms (I get a mild stomach ache and some heartburn, nothing major)?

 

I fully intend to stick to this diet, as much as I may not be thrilled about it, but I'm trying to make sure I know how I handle myself when I'm out (already went out once, had to pass on the eating).  Thanks for any advice.


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

So, your saying that your family would be insulted by you taking care of your health? Your family expects someone with a severe peanut allergy to eat the Pb cookies they made and die? They think a person with diabetes can't take a minute to check their blood sugar and give them self insulin? Why would you want to associate with these evil people?

Ok ..maybe that is a bit extreme...but do you see the point? They wouldn't want you to poison yourself. You just need to explain it to them. Then bring your own food for awhile, at least. Until you understand eating gluten-free better and can figure out if you can eat any of their food & how to deal with these gatherings. You can say your doctor said so....that works for many older family members.

Z3ro Newbie

So, your saying that your family would be insulted by you taking care of your health? Your family expects someone with a severe peanut allergy to eat the Pb cookies they made and die? They think a person with diabetes can't take a minute to check their blood sugar and give them self insulin? Why would you want to associate with these evil people?

Ok ..maybe that is a bit extreme...but do you see the point? They wouldn't want you to poison yourself. You just need to explain it to them. Then bring your own food for awhile, at least. Until you understand eating gluten-free better and can figure out if you can eat any of their food & how to deal with these gatherings. You can say your doctor said so....that works for many older family members.

Thanks for the response, and that certainly is the long-term plan.  In the short term, both mine and my in-laws can be a bit...obtuse.  They're good people, but sometimes I wonder.

 

But what I'm really looking for is an answer; when the choice is gluten or starve, should I just dive in?  I can't see a problem when talking about one crumb=loaf of bread.  If not, why not?

shadowicewolf Proficient

Ideally you should always have something with you (such as trail mix or fruit).

The issue with your problem is that once you are off gluten for a while and then reintroduce it, your symptoms could be worse than what you originally had before the dx.

 

Personally, I would do without. It is not worth it to me.

cyclinglady Grand Master

Karen's advice, as usual, is excellent.

 

At parties and family gatherings (which I usually try to host), I bring my own food (and eat prior to going too).  I bring enough to share and then I'M the first to go through the line before someone can cross contaminate the dishes I brought (I help with the set-up and wash off metal serving spoons too).    Email or mail articles to you in-laws and talk about celiac disease.

 

Here's why continue to eating it during "parties" is completely wrong.  My initial symptoms were simply anemia and Hashimoto's Thyroiditis (had it for almost 20 years) and since I have a genetic anemia, docs didn't catch the iron deficiency anemia.   

 

About five weeks ago,  I fractured one of my vertebrae doing NOTHING!  I did not fall, I was not in a car accident.  My bones have been compromised (bone scan in two weeks) because of celiac disease. 

 

IF YOU CAN'T PREPARE FOOD FOR A PARTY, THE ANSWER TO YOUR QUESTION IS TO STARVE DURING A PARTY! 

 

Yes, you can cheat and not feel the effects short term, but long term problems can be devastating!  I can not get back on my bike until I get my bone scan results.  I can not run because it bothers my healing back.  Pain is gone -- just tweaks, but I have back numbness not to mention the fear that I might just spontaneously fracture another vertebrae or something else!

notme Experienced

 

 

IF YOU CAN'T PREPARE FOOD FOR A PARTY, THE ANSWER TO YOUR QUESTION IS TO STARVE DURING A PARTY! 

 

 

been there, done that.  if i get glutened it takes 2 days for it to fully hit me.  then it's another 12 of feeling like i've been hit by a truck.  not worth it.  

 

most of us have some sort of food with us at all times, lolz.  ya never know when you're going to be stuck without anything to eat.  just avoid having to make that choice by thinking ahead - make a sandwich, bring a dish to share, as others have said.  good luck! 

Adalaide Mentor

No one is going to die if they go to a party and don't eat for a few hours. So you may be hungry. So what? So someone may get all butthurt over the fact that you don't want to spend the entire party in the bathroom with exploding bowels. Again, so what? If that is the kind of people hosting the party, you can either explain to them with the patience of a saint that it really just isn't safe for you to partake and they can be understanding, or you know not to go to their parties any more. You now have a built in jerk-o-meter. (Yeah, I stole that... sue me. :P)

 

Do you really prefer to be sick, risk your long term health, spend a day (maybe more) in the bathroom and in agony, plus all the other symptoms that you may get... over someone's feelings about what you put in your mouth? Are you freaking serious?!?! If they don't like that you care about your health, they're jerks and you don't need to associate with them. Family or not.


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Thanks for the response, and that certainly is the long-term plan.  In the short term, both mine and my in-laws can be a bit...obtuse.  They're good people, but sometimes I wonder.

 

But what I'm really looking for is an answer; when the choice is gluten or starve, should I just dive in?  I can't see a problem when talking about one crumb=loaf of bread.  If not, why not?

I don't understand the choice of eat gluten or starve. You know you will be wanting to eat, so you can bring something. Keep a packet of nuts or a gluten-free granola or protein style bar with you, always.

If the choice is to eat rat poison or starve, which would you chose? Especially because we you aren't talking about really " starving ".

I get the feeling you are either in denial about the severity of Celiac Disease or you are playing with us a bit.

GottaSki Mentor

Thanks for the response, and that certainly is the long-term plan.  In the short term, both mine and my in-laws can be a bit...obtuse.  They're good people, but sometimes I wonder.

 

But what I'm really looking for is an answer; when the choice is gluten or starve, should I just dive in?  I can't see a problem when talking about one crumb=loaf of bread.  If not, why not?

 

One crumb can be just as harmful as a loaf of bread...the point here is until you remove ALL gluten your body will continue to attack itself.  If you understand that you should not eat a loaf of glutenous bread than understand that a crumb of that loaf is not acceptable either.

 

Either remove gluten or don't....but you are risking a lot more than just being uncomfortable...a crumb / a loaf -- neither is acceptable with Celiac Disease - ever.

 

Imagine those that are unaware of how to prepare safe food for you are sprinkling that food with broken glass - how much are you willing to ingest?

1desperateladysaved Proficient

The theory of eating a little and trying to "fit in" until you try it seems good to my family.  Many of us who react to minor cross contamination do not care to repeat the experience.  I am pretty sure you will find that too, if you accidently get gluten.  I would not even consider having gluten on purpose.  I  have more intense reactions after going gluten free.  I think my body  is now able to tell me something horrible is happening to it and it does.

 

I think it is right not to surprise your family with it.  Last time I went to a extended family meal, I e-mailed family members beforehand to let them know I would be bringing my own.  I blamed it on celiac disease, and said that I was willing to bring food for anyone else that had celiac disease.  Nobody stepped forward.  I included my disappointment in not sharing their food, and my longing to be in their company in spite of it.

AlwaysLearning Collaborator

First, congratulations on getting a diagnosis and starting on gluten free. That is HUGE and I do hope that the positive affects on your body start to appear quickly as they do make it easier to keep your resolve up.

But I'm going to skip talking about the effects on your digestive system that you can't see. Others have already covered it.

Rather, I'll stick to some of the reactions you can expect to have if you do eat gluten after already going gluten free. Everyone's reactions do vary but these do seem fairly typical.

• If you have a bad reaction to being glutened, you may have diarrhea that starts while you are still at the party. If you are really sensitive, you may even throw up.

• If you have a lesser reaction, you can still expect to have an upset stomach, which may include lots of gurgling, gas, bloating, etc, with or without diarrhea later.

• Even if you got lucky and missed the digestive reactions because you really tried to avoid the foods that contain gluten and only got a slight cross contamination, you'd still be likely to get the mood and headache reactions, and that means getting irritable (a nice way of saying really angry) and getting a headache (even as bad as a migraine level). And even before the anger kicks in, you will already be off your game when it comes to social skills. 

• My reaction normally includes my sinuses which means I'll start sneezing, have a runny nose, and get phlegm in my throat as well the sinus pain and pressure.

• Some people will also have skin reactions which could be as simple as having a bit of an itchy rash, to as much as breaking out in hives. 

• After you get through those initial reactions that may resolve themselves in the first day or two, you can look forward to feeling fatigued, lethargic, and unmotivated (brain fog) for as few as 2-4 days to as much as 2 weeks after being glutened. And as far as I can tell, this is true for everyone, no matter how small the contamination or how severe their reaction.

So all issues of long-term affects and hidden damage to your intestines aside, my question would be, do you really want to risk having a reaction while you are at the party and to then suffer the recovery as well? 

Okay, that said, being in your first week of being gluten free, you may not have as strong a reaction as all of that. Chances are you haven't managed to completely eliminate cross contamination from your own kitchen yet or still have some hidden sources of gluten in your foods. But even then, I'd expect some level of reaction.

Personally, I'd much rather have my family or friends have a perceived insult because I didn't eat their food than to actually have a reaction and have them be insulted by something I said or did when in the midst of it, because they definitely won't understand that! And you often don't even realize that you are in the midst of a gluten reaction until after you've gotten all riled up about something that you would normally overlook or have started to feel lousy. 

I know there are some threads on this forum somewhere about how people react when they've been glutened. I'd track one of them down prior to the party to help you bolster your resolve not to be poisoned. You're likely to have quite a few hiccups from true accidents in the near future, and they'll be tough enough to get through, so I'd avoid all of those that you know are a risk. And you're going to have to start refusing their food at some point, so it may as well be now.

But you will succeed. And this forum is definitely a great place to be for help getting through the early stages.

whitepine Apprentice

In my experience, once I started the gluten free diet and I ended up accidently getting into gluten a year after, the reaction was way worse than before. I understand how hard it is to be able to go to some ones house and pick through stuff/ask around. Sometime people are really accommodating other times they aren't. For example, if you are going to a family dinner and there's turkey, ask if it could be cooked unstuffed instead etc. It's hard to change peoples traditional cooking so being gluten free has made me the host more often for dinners so I know that things are gluten free and nothing will be contaminated. 
Otherwise I just stick to what I know at parties/dinners. I wont be able to eat as much as most people but I will pick what I know is safe to eat. Some people won't do that because their reaction is incredibly severe But I don't think it would be a good idea to dive in and eat, there are always options. If you eat gluten from time to time , you are just setting the clock back and your healing will be delayed over and over Even if you have to bring your own food, if people are upset about it, they get over it. You have to explain to them over and over that it's a disease and not a fad diet choice. If they choose not to believe you or whatever then they are obviously not the best people to have around. Friends and family should always support one another when it comes to being healthy and getting better especially if their illness is chronic and diet is the only way to control the symptoms.



 

mbrookes Community Regular

I liked the idea (who was it?) of blaming it on the doctor. That is hard to argue with. I have said (almost whining!) "My doctor says I can't have even a bite. He's driving me crazy, but I have to do as he says". Blame it on the doctor. I promise you he won't mind and it will get you off the hook.

kareng Grand Master

I liked the idea (who was it?) of blaming it on the doctor. That is hard to argue with. I have said (almost whining!) "My doctor says I can't have even a bite. He's driving me crazy, but I have to do as he says". Blame it on the doctor. I promise you he won't mind and it will get you off the hook.

I do that. I say the doctors at The Univ of Chicago Medical Center Celiac Center say " insert what you want them to know here". People think they are my doctors and I just let them think so. They have lots of advice on their website, so they are sort of our doctors. :)

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.