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 Make Boyfriend And Friends Understand


charlotte-hall

Recommended Posts

charlotte-hall Apprentice

Hi everyone,

I'm 15, been diagnosed for 4 months, and still struggling a lot with my health, not feeling normal yet.

And my friends and boyfriend don't really understand, and don't take it seriously.

I'm super sensitive and I've been researching and have found that even if you kiss someone who's eaten gluten you can get contaminated. And I've spoken to my boyfriend about this and he's not willing to read books about celiacs or try and gluten free foods or anything..

And with friends and boyfriend like that it just makes everything a whole lot worse!

Any ideas?


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



Celiac.com Sponsor (A8-M):



Stubborn red head Apprentice

I know and remember being sick and on a restrictive diet at 15. Its really tough. The situation with your boyfriend and friends is a difficult one. Post people at that age don't get the concept of a food allergy unless they have one. I do sagest, not forcing it on them, If they dont want to read the books, pamphlets, web sites, or any other information. You need to focus on you and your health right now, if you feel like you get sick after kissing him from him eating gluten then quit kissing him, if he wants your kisses then he will avoid the gluten to be able to kiss and be near you. Your friends on the other hand, I would keep it simple. Tell them you have a wheat allergy any that has flour in it, you cant have.

When it comes to outsiders don't get it. Best rule of thumb is keep it sumple stupid... Not calling you stupid, but most people have a tendency to over complicate things. gluten-free is not a simple thing but for those that dont have to follow it dotn need to know the whole issue, Wheat allergy works for most people.

jizzzzie Newbie

I know how you feel. I was diagnosed two years ago (I'm now 14) and my boyfriend and I were together for three years (broke up over the summer..) Last year he would express how much he wanted to kiss me, and I tried to get him to understand. He was veRY UNderstanding which was so helpful. He said he would go on a gluten free diet just to kiss me - unfortunately he didn't understand exactly what that meant and how much it would restrict his life - it doesn't mean just not eating bread or cookies (normal oneS).. I told him it would be too hard, and we promised ourselves when we got older he would go totally gluten free.

He also said that he researched, and couples who had one person gluten free, the other could just brush their teeth really well with gluten free toothpaste, but being the ultimate worrier and I also have the worst phobia of getting sick, I said no. I actually made up a lie that I have a special kind of celiac disease, which means I'm SUPER sensitive.. I feel really bad about it, but I was so obsessed with staying gluten-free clean I felt like I had to.

So we ended up sticking to the other physical things, and kissing on the cheek, head, other places on the face besides the mouth. Of course he could only kiss me there since I was terrified that his shaving cream or aftershave had gluten in it as well!

Luckily my friends were also understanding, kind of.. One friend, said she WANTED to have celiac disease, just because my gluten free pretzels (glutino by the way, everyone's a fan!) were so delicious. That made me so angry!!! I tried to tell her NO you do NOT want to.. because it's not just getting to eat yummy alternatives.. besides you can eat them when you don't have to avoid others ANYWYA!!!

I sort of gave up on making them fully understnad... though

I just kept my food to myself, and if I was invited somewhere, I brought my own as well. I didn't bother asking people to get special food, or if they asked, I politley refused and said not to bother, I'd be content with my own stuff thans. I have a wonderful best friend though, and even though she doesn't understand what it's like, she treats gluten like the black plauge when I'm around! <3 Watching out for me, even though I don't need it I'm quite thankful. :)

Tell your boyfriend that you will get very sick and it will contribute to further fatal illnesses later in your life if you get gluten, and kissing him is posing a risk. If he is a true heart boyfriend, he would rather you not get sick, because he cares about you. He doesn't have to read anything as long as he beleives you. Send him the link to wheere you read the thing about kissing though, just so he knows youa re teling the truth. And make sure you express how you love to spend time with him, so it doesn't seem like a way of sneaking out of the relatihonship.

If he refuses to cooperate, though, then I don't see the whole relathionship working There needs to be aggrement on both sides.. But health comes first.

Goodluck

maximoo Enthusiast

kick him to the curb & just tell your friends that gluten "messes you up" plain & simple. Bring your own food when you hang out with friends,etc. Good Luck!

Gf Princess182 Rookie

Hi everyone,

I'm 15, been diagnosed for 4 months, and still struggling a lot with my health, not feeling normal yet.

And my friends and boyfriend don't really understand, and don't take it seriously.

I'm super sensitive and I've been researching and have found that even if you kiss someone who's eaten gluten you can get contaminated. And I've spoken to my boyfriend about this and he's not willing to read books about celiacs or try and gluten free foods or anything..

And with friends and boyfriend like that it just makes everything a whole lot worse!

Any ideas?

I know exactly how you feel. I got so frustrated with the guy I was dating so I printed him out a little booklet for his family and for him as well. Unfortunately they still didn't get it. It's really hard to be a celiac and in the dating world, I hate constantly worrying about the food at dining places.

You need to worry about your health and well being, if they can't understand that then kick them to the curb. Someone who understands will come along, you're only 15. When I was diagnosed I was 16 and I know how awful it is those first few months. I know it feels like you're a prisoner, but I've been gluten free for 2-3 years now and it does get better and easier.

I'm an extremely sensitive as well, and I have been contaminated by kissing someone who has eaten gluten. The only advice I can offer you as far as helping people understand, keep explaining. It may take a while, but some people will understand. I wish you luck :)

lostnaphotograph Newbie

Hi everyone,

I'm 15, been diagnosed for 4 months, and still struggling a lot with my health, not feeling normal yet.

And my friends and boyfriend don't really understand, and don't take it seriously.

I'm super sensitive and I've been researching and have found that even if you kiss someone who's eaten gluten you can get contaminated. And I've spoken to my boyfriend about this and he's not willing to read books about celiacs or try and gluten free foods or anything..

And with friends and boyfriend like that it just makes everything a whole lot worse!

Any ideas?

I totally understand what you are going through. Its very hard to get people to understand the concept of it all. Especially a boyfriend. I was diagnosed when I was about 15 and I am now 21. I tell my boyfriend tho that if he wants to kiss me, he has to brush his teeth frist. It works great that way too. He doesn't mind brushing his teeth after eating wheat before we kiss. Hope this helps and good luck!!

  • 3 weeks later...
JonsLoveBugg Newbie

I know how you feel. I think we all have been there at one time or another. I'm 20 and have been gluten free for 2 years but was pretty much food free for 3 years before that because nobody could figure out what was making me sick so my food intake was very little because I didn't want to feel worse! I got very fortunate with my boyfriend. We live together and just bought a house together but my house must be gluten free and he has sacrificed gluten for me. He will still eat it at work and when I'm not around but when were together he does not eat gluten. I know it may be hat for your boyfriend to understand now but if he truly loves you he will educate himsel on the subject because he shouldn't want to risk your health because he wants to eat a sandwich! And with your friends; I've found that my best friends all understand and are very conscious of it but my not so close friends don't really understand. And there not going to. I have to exaggerate the severity of my reaction to gluten so my friends are EXTRA careful when they want to cook something for me or whatever. That's been the best way I've been able to cope with it!

Good luck!

Natalie


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



Celiac.com Sponsor (A8-M):



Newtoitall Enthusiast

All I have to say, is be glad your not a guy. I find guys are much more willing to sacrifice for a girl then girl's are for a guy, having to be the forward one usually makes the first kiss awkward as F when you have to find a way to be smooth about saying "so hey yeah, I can't kiss you unless you go brush like a fiend! with .. this kind of toothpaste.. ahaha it's funny to think about it because it will never happen. I wish you the best of luck with it though. Would love to have good advice on that one =P

If I come off as insensitive, my bad, I'm not saying all girls are that way, just alot of them find it way easier to just move on, I can't blame them either.

  • 5 weeks later...
SmnthMllrX Newbie

After I went gluten-free I found out who my real friends are. Not to make you feel bad or rub anything in but I have friends who throw whole gluten-free parties when I'm the only one attending that is gluten-free. They would never decide to go out to dinner and pick a place that I cannot eat at. As for my boyfriend, when we go out to eat he eats off of the gluten-free menu. If he does eat gluten he always makes sure that he brushes his teeth really well and uses mouth wash to get anything he may have missed. When we move in together (hopefully soon) he was very accepting when I explained why I wanted our place to be a gluten free one. He loves me and he loves me healthy.

You'll find REAL friends and there are guys out there who will adapt to your diet to make sure you don't get sick. I swear they are out there and when you find them hang on to them.

Good luck! It gets easier.

rml97 Rookie

I was just diagnoised with a severe gluten intolerance in September; I turned 14 in October. I became so sick and am now VERY careful. I always have purell with me and use it before putting anything near my mouth. It took so long to find out what was wrong with me and in the process of not nowing I lost a lot of weight and had to stop ALL physical activity. 2011 was the worst summer of my life! So I completly understand what it's like to have to try and explain what it means to be gluten free to friends and family, some are more willing to listen and try to understand than others... My grandmother has been super supportive and so had my parents and sister her boyfriend even looks out for me when it comes to gluten (his mom even made me a batch of gluten-free brownies...although I was too nevous to try them. I wasn't sure how careful she was about cross contamination, but everyone else seemed to enjoy them). My reaction to having gluten is almost instant so I do everything possible to stay gluten-free.

One way that I have found helpful to explain my reaction to gluten is explaining to people that what happens when I have gluten is nothing like a peanut allergy or anything like that. I don't get hives or anaphylactic shock.... When I have gluten everything is internal, you can't see it happen, I can just feel it........

Relationships with me are pretty much non-existant... Now that I'm gluten free my parents have officially allowed me to start dating purley becuase they know there won't me any kissing. I don't even let my family get anywhere near me without brushing their teeth and washing their hand after they have gluten, nevermind a boy...

  • 1 year later...
Herreralovv Rookie

I kno how u felt. My husband didnt quite understand wat celiac was, and i explained it to him, and now he doesnt even eat gluten food in front of me, just to not give me temptations. I had self diagnosed myself at first, and everyone thought i was just inventing this disease, they thought i was loosing weight because i wasnt eating bread and stuff like them. they was just depressing me more. But then as i continued the gluten free diet, they actualy understood that i wasnt making it up( and plus i got the test results later). But my friends, well at least the ones i thought were my friends , didnt even bother to see if i was okay or something. Im just happy i have a great famiy who undertands and always make gluten free food when i come over. Friends come and go, family are their to stay.

  • 2 months later...
iloathegluten Newbie

I'm 23 now and totally know what you're getting at with people not understanding the disease or what it's like to have to be hyper vigilant about EVERYTHING that comes in contact with your mouth. My mom once saw me reading through the ingredients on an antacid bottle and snapped at me that "They wouldn't put gluten in medication that's meant to make you better!". Completely false. Gluten can be found in anything... She was frustrated with me that night and insisted the glutening I'd experienced from Applebee's was in my head. (It wasn't. The tortilla chip strips were fried in a common frier... ) She used to harp on me about overthinking things and still does occasionally. She'll often think I've simply psyched myself out when I've been glutened if the amount or source of it doesn't make sense to her. She's since gotten MUCH better. It was helpful for her to be able to see the damage it to me after a recent glutening. Rather than try to hide the bloat behind baggy clothes, I decided to wear a shirt that made it incredibly obvious I looked five months pregnant. When she commented on it, I told her something along the lines of "This is what cross contamination does. Now imagine if I ate an actual piece of bread?" She was freaked out enough by seeing how distended I looked in addition to how many times I ran to the bathroom that day to believe it was real. She did a lot of research on it and now is one of the very few people I trust to make me a meal now.

 

My advice, which is very similar to what others have said, is to try and illustrate with really concrete examples why gluten makes you so sick. If the damage is visible on you, like a really bloated belly or a rash, maybe you could show them that (I definitely don't mean purposefully gluten yourself though!) Otherwise I've had luck asking them to remember their worst experience with the stomach flu, and then ask them imagine that illness happening every singe time they ingest something. I've seen some visual representations online that show a crumb next to a piece of bread in order to illustrate how little gluten is required to make a Celiac sick that are helpful too. Show them these as well. Most people will come around eventually. I've encountered a few really ignorant people who don't think any food allergies or intolerances exist, but they are rare. Most people simply have no clue how careful we have to be!

 

The other thing I've done is brutal honesty. I think most Celiac sufferers have had an experience where someone well-meaning tried to make them something gluten free but ended up making them sick. The first few months I was gluten free I'd lied and tell them I felt fine so I wouldn't hurt their feelings, but I think it makes them more aware of just how serious it is if they realize that their careless prep methods caused you illness...If someone accidentally makes you sick, definitely let them know. It doesn't have to be in a rude way, but this got one of my closest friends to be a better ally about gluten.

 

As far as kissing goes, I agree with making your boyfriend brush his teeth first. I'd probably also ask he rinse his mouth out thoroughly with water or mouthwash. Make sure the mouthwash and toothpaste is gluten free though!

 

Hope it helps!

  • 7 months later...
Hobbes Rookie

Hi everyone,

I'm 15, been diagnosed for 4 months, and still struggling a lot with my health, not feeling normal yet.

And my friends and boyfriend don't really understand, and don't take it seriously.

I'm super sensitive and I've been researching and have found that even if you kiss someone who's eaten gluten you can get contaminated. And I've spoken to my boyfriend about this and he's not willing to read books about celiacs or try and gluten free foods or anything..

And with friends and boyfriend like that it just makes everything a whole lot worse!

Any ideas?

 

This makes me incredibly frustrated. You could try to explain to your boyfriend that you have a DISEASE. If he found out you were allergic to peanuts, he wouldn't try to throw them in your face, would he? It's a disease, and he needs to treat it like one. I understand that it can be hard for him to understand, but it's honestly not that hard to put into practice. I don't know how sensitive you are, but for most people simply having their boy/girlfriend brush their teeth after eating gluten is enough to stay gluten free. 

 

Honestly, just refuse to kiss him after he eats gluten unless he brushes his teeth. He will also probably see you get glutened at some point, sometimes that's what people need to truly understand that this is something serious for you.

 

I wish you the best of luck! And don't despair. There are plenty of great people out there that will understand and accommodate to you. I've been with my girlfriend for 9 months now and she is completely fine with it. She even defends me in front of other people!  :)

 

Take the same approach with your parents. Simply refuse to eat anything with gluten in it, and do your research well. No parent will want their child to starve, so they will inevitably buy you gluten free foods.

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.