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 Deal With Unsupportive Friends?


madminx

Recommended Posts

madminx Rookie

Hello everyone, 

 

I've been gluten free since January. i don't have an official diagnosis, but I plan to see a doctor soon to try to get diagnosed. I don't have health insurance, so not sure how that will go. 

 

Anyway, I've told all of my close friends about my struggles with what I believe to be celiac disease since January. At first they were generally supportive. Recently, more and more I've been getting the impression that they don't believe that my symptoms are as severe as I claim them to be. When I complain to them about accidental glutenings and that I usually get sick for 1-2 weeks from just 1 meal with a small amount of gluten (including from cross-contamination), they react to me with doubt and are very dismissive. For example, I was accidentally glutened recently at a restaurant. I told my friends about it, and they all said it's impossible that gluten would cause me to feel like crap for a week or more, even after I told them I get this same set of symptoms for the same amount of time every single time I accidentally eat gluten. And they said there's a mild cold/flu thing going around, so OBVIOUSLY I had that and it wasn't gluten related. 

 

I don't really know what to do anymore because I'm not making it up and I'm not exaggerating, and their consistent doubt and dismissiveness is making me resent them a little. I mean, they know very little about celiac disease/gluten intolerance. I've done extensive research on it since January. And how can they presume to know how I'm feeling and what symptoms I'm having? They're not in my body. They think it's a placebo effect. Then how do they explain the several times I've been glutened and was in denial about it at first till the symptoms get so bad that it's undeniable? And all the chronic health issues I had that magically went away after I started the gluten free diet? 

 

I'm sure they'll believe me after I get officially diagnosed, but I don't even know if that's going to happen because I've heard that you have to eat gluten for several months in order to get diagnosed, and I'm not willing to be sick and miserable for months just to get diagnosed. 

 

How do you all deal with people who constantly doubt you and think you're making it all up? 


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



Celiac.com Sponsor (A8-M):



w8in4dave Community Regular

I would either just tell them, Because I am a straight forward person. Well believe me or not it happens that way. All my friends have been really supportive. I don't know how old you are, but I am 53 y/o and I think people that are a "lil" older tend to be a lot nicer about things of this nature. 

And really there are people here that are officially Dx'd and still no support from family and friends. I wouldn't really worry about it myself. But just to give you an inside. Look up restaurants in your area or restaurants where ever you are going to see what ones have a gluten free menu. After being glutened at restaurants a few times, I tend to go for the meals that are naturally Gluten Free. Like a Salad that doesn't have croutons, or a breakfast with potatoes and eggs, no toast. ... It seems to be what works for me. I fortunately do not get sick for a long time. It is an a few hrs. But everyone reacts differently. 

I know I tell ya if I was in your shoes I'd feel the same way about getting Dx'd , If they told me right now that my test was fubbled up and they wanted to do it again, so I'd have to go on Gluten. I'd say nooooo thank you. But some people seem to need that Dx to be faithful to the diet. Because they have not been "Truly) Dx'd ... It is a personal decision for you. 

And don't forget! You can always find new and  supportive friends!! 

flowerqueen Community Regular

You shouldn't have to go through pain and illness just to prove it to your 'friends'. I had to eat gluten regularly for 6 weeks before my diagnosis and in was hard going, I can tell you! You should not have to 'prove' anything, you know your own body. Also everyone's different when they have accidentally consume gluten, BUT, are you sure you have only been glutened the once and not several times over a few days, if you are being ill for so long? A food journal would be useful to find out for sure.

Personally, I'd be of the view, "It's my body, my life, my business" and if they didn't like it, they can jolly well lump it. You've always got us, here on the forum, to discuss any issues with.

mbrookes Community Regular

Maybe, just maybe, you have gone overboard in talking about the problems with gluten. People do get tired of hearing about any sickness. Try not talking about the problem for a while and see if they are more receptive when you mention it occasionally.

bartfull Rising Star

Yep, when I am not feeling good, close friends will ask if I've been glutened, but other than that, if I have to skip out on a planned event, I just say I'm not feeling well and leave it at that.

whitepine Apprentice

I tend to not tell my friends about it mostly because they really don't understand and I can't expect them to. It really only comes up if we are eatting together, but even then I go about my gluten free diet as normal regardless of their comments or sighs of disgust.

I rarely tell my friends about my experiences being glutened and really only disscuss this with my partner who believes and has seen me glutened. I learned at a really young age, when I was chronically ill, that people aren't interested in hearing about illnesses all of the time. Try to find support in other parts of your life, like here because we all know what its like, and accept that your friends will never get it. Hopefully they will tolerate it rather then torment you about your choices.

 

Honestly, I take the time with my friends, who don't understand my illness, as a chance to disconnect from the way I am feeling or my bad health experiences. It gives me the time to forget about it and focus on other aspects of my life.
 

1desperateladysaved Proficient

My MD did warn me that I would drive everyone crazy talking about this for 6 months!  Only just recently, some are starting to listen, since it is no longer deniable to them!

 

D


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



Celiac.com Sponsor (A8-M):



Kassia Newbie

It seems there are a couple of issues at play here: your desire to get diagnosed coupled with your (legitimate) worries about going back on gluten for a diagnosis; your lack of insurance because these tests can get pricey; and, finally, the skepticism of your friends. The bottom line is that you know how being gluten-free feels, and you know how you feel when you've ingested gluten. Your friends can express all the doubts they want, but they clearly don't know what happens when a person ingests gluten.

 

If you want to continue hanging out with this group, you're likely best served by carrying on with your diet and ignoring their doubts. As long as they're not sabotaging your diet, you can feel good about your course. If the relationship turns from skepticism to sabotage, then you have a serious problem.

 

Some people really get it when it comes to be gluten-free. They may not understand the nuances, but they understand that gluten makes us sick. Others simply don't or won't. There's no point in trying to convince them; if you're lucky, they'll come around when they see how well you're doing. 

eers03 Explorer

Try suggesting a restaurant that you are comfortable with as much as possible.  If the gathering is already arranged, try eating before, after, or bring something of your own.  I whip stuff out at the table all the time.  It was awkward the first time but it really isn't a big deal.  After 5 minutes the novelty wears off and you are just eating like everyone else.

 

I wouldn't write off any friends unless they outright make fun of you or make you feel guilty by intent.  At the same time, don't just rollover and be submissive to their doubts.  My friends were really cool about letting me talk about it at first.  Eventually, I had to apply some self awareness and make a concentrated effort to not make it a talking point unless someone brings it up.  When it comes up, if I look cool and casual, they will take it cool and casual usually.

 

Them "Hey, want to meet us at BW-3 for wings?"

 

Me "Definitely, lets meet up!  Let's go to (fill in the blank) instead because I can't eat their wings, they put them in a fryer with other stuff the has breading in it."

 

Them "That's right, I forgot about that.  But you can eat at (fill in the blank)?"  

 

Me "Yep"

 

Them "See you there"

 

That's how it usually works for me...  Good luck!

dilettantesteph Collaborator

I would try to think of it from their point of view.  Before I was educated about this, I wouldn't have believed it either.  Many of us become somewhat obsessed when we first find out what has been causing us so much grief for so long.  After awhile you realize that what interests you isn't necessarily what interests others.  Then you can get back to the latest fashions, TV shows, books and gossip.

w8in4dave Community Regular

It actually seems the more people I tell, or hubby tells, the more we find people know about Celiac, they have a cousin or uncle. Or a friend that has it. Sometimes people don't want to deal with stuff they don't understand.  I guess I should feel more blessed because none of my friends have been un supportive. But then again these are the friends that have seen me go thru so much in the last few years. running to the rest room all the time, and not understanding why I am in there most of the time after we eat. So now they get it! So what I am getting at is maby if you educated them more about your problem the would understand and be more supportive. 

eers03 Explorer

In unrelated news...  I was sitting in church the other day and there was a reference to wheat or bread in the bible...  I leaned over and told my girlfriend, "My Jesus doesn't eat wheat."  HAHA!  Okay, so maybe I thought the comment was funnier than it really is but she looked at me, laughed, and started shaking her head.  Your talking about interactions with family and friends made me think of that for some reason.

w8in4dave Community Regular

Haha Thats pretty cute eers03

MChase Apprentice

Hello everyone, 

 

I've been gluten free since January. i don't have an official diagnosis, but I plan to see a doctor soon to try to get diagnosed. I don't have health insurance, so not sure how that will go. 

 

Anyway, I've told all of my close friends about my struggles with what I believe to be celiac disease since January. At first they were generally supportive. Recently, more and more I've been getting the impression that they don't believe that my symptoms are as severe as I claim them to be. When I complain to them about accidental glutenings and that I usually get sick for 1-2 weeks from just 1 meal with a small amount of gluten (including from cross-contamination), they react to me with doubt and are very dismissive. For example, I was accidentally glutened recently at a restaurant. I told my friends about it, and they all said it's impossible that gluten would cause me to feel like crap for a week or more, even after I told them I get this same set of symptoms for the same amount of time every single time I accidentally eat gluten. And they said there's a mild cold/flu thing going around, so OBVIOUSLY I had that and it wasn't gluten related. 

 

I don't really know what to do anymore because I'm not making it up and I'm not exaggerating, and their consistent doubt and dismissiveness is making me resent them a little. I mean, they know very little about celiac disease/gluten intolerance. I've done extensive research on it since January. And how can they presume to know how I'm feeling and what symptoms I'm having? They're not in my body. They think it's a placebo effect. Then how do they explain the several times I've been glutened and was in denial about it at first till the symptoms get so bad that it's undeniable? And all the chronic health issues I had that magically went away after I started the gluten free diet? 

 

I'm sure they'll believe me after I get officially diagnosed, but I don't even know if that's going to happen because I've heard that you have to eat gluten for several months in order to get diagnosed, and I'm not willing to be sick and miserable for months just to get diagnosed. 

 

How do you all deal with people who constantly doubt you and think you're making it all up? 

I am sorry you have to deal with this.  I am new (haven't been officially diagnosed).  I have my consultation with a GI next week. My primary says I definitely have Celiac or Ulcerative Colitis or both.  My Mom thinks this is because of all the "crazy" diets that I have been on, which I am not sure what I am talking about.  She also thinks that I just need to eat better and it is easy to implement a gluten-free diet.  She thinks that I am sick all the time and that this is no big deal.  I am dreading visits because in the past when I have turned down junk food (I don't eat sweets), sodas, etc, she tells me that just one won't hurt me and seems very upset when I don't give in.  I am almost 40 and still don't how to deal with it.  I cannot imagine how to respond if and when I have to go gluten-free.  I wish you luck with dealing with your friends.  

GF Lover Rising Star

The words "unsupportive friends" seem to be an oxy-moron ;)

1desperateladysaved Proficient

I am sorry you have to deal with this.  I am new (haven't been officially diagnosed).  I have my consultation with a GI next week. My primary says I definitely have Celiac or Ulcerative Colitis or both.  My Mom thinks this is because of all the "crazy" diets that I have been on, which I am not sure what I am talking about.  She also thinks that I just need to eat better and it is easy to implement a gluten-free diet.  She thinks that I am sick all the time and that this is no big deal.  I am dreading visits because in the past when I have turned down junk food (I don't eat sweets), sodas, etc, she tells me that just one won't hurt me and seems very upset when I don't give in.  I am almost 40 and still don't how to deal with it.  I cannot imagine how to respond if and when I have to go gluten-free.  I wish you luck with dealing with your friends.  

My Mom thought my diet was "crazy" too.  Moms do care.  I hope you will get to the bottom of it with gluten and find health in it.

D

notme Experienced

In unrelated news...  I was sitting in church the other day and there was a reference to wheat or bread in the bible...  I leaned over and told my girlfriend, "My Jesus doesn't eat wheat."  HAHA!  Okay, so maybe I thought the comment was funnier than it really is but she looked at me, laughed, and started shaking her head.  Your talking about interactions with family and friends made me think of that for some reason.

lolz, eers!  :D mine too, either!  every time they talk about the wheat and the chaff, i think to myself, well, i guess i'm stuck with chaff...................   my husband has played Jesus every time they need one for easter (he's a long haired hippie type), etc, so i guess i got an 'in' being married to 'Jesus' ;)

 

The words "unsupportive friends" seem to be an oxy-moron ;)

lolz, colleen!  :lol:

 

i have found out that i have 2 or 3 sub-groups of 'friends' (let's get real, i only have one friend lolz) i have the ones who quit inviting me to their shindigs ("oh, you can't eat anything and it's a dinner.....")  the ones who forget every 2 seconds and try to feed me (mostly church peeps) the ones in the small circle who want to do *anything* they can to accomodate me (i tell them i'm fine, but they fuss anyway, make sure they bring out the unopened bag of whatever.... and plop it down in front of me..... dude, i don't LIKE those just because it says gluten free on the box/bag, doesn't mean i HAVE to eat it????  STOP IT)    you'll find out who's who.

 

i wish my mom was still around so i could tell her:  look, mom, they finally figured out what was wrong with me!  she always worried so much - i can't tell you how many doctors she took me to.  if she had a couple of more years with the internet, she would have figured it out.  (and i wouldn't have listened to her!  lolz!  love you, mom)  my point is, take it easy on mom  :) 

Auntie-Manda Apprentice

I know how you feel! My sister thinks I'm making it all up. I told her about how I got deathly ill after taking communion (my pastor said he'd get gluten-free wafers and gave me a regular one instead without telling me). She was like, "really?!? From just one communion wafer?" Well, yeah, it's a lot of gluten! She's always asking, "are you still doing that gluten free thing?" Yes, I'll be "doing that thing" forever so I can be able to enjoy life and not spend it curled up in a ball crying in pain.I tried to tell her about how miserable I was with my daily headaches for 12 years, and when that switched to daily migraines in January. Her response: "well, everyone has headaches." (in a tone of voice that implied that I'm a hypochondriac).

 

People like that are the only reason why I would consider getting an official diagnosis ("real" celiacs give me crap, too. Like their issues are genuine & mine are made up. So sad!). I can tell myself that they are just ignorant, and it doesn't matter what they think because I am the one in control of my health. But it's still hurtful. I guess just try to keep educating people if they will listen. 

Auntie-Manda Apprentice

Oh, and if I get annoyed enough, I will say, "You're right. I must be making this up for attention. It's just so much fun not being able to eat my favorite foods anymore." People are so dumb! Why would we make this stuff up?!?

w8in4dave Community Regular

Absolutely!! I agree it is too hard of a diet to follow. If you are not seriously having problems!! Celiac or sensitive!! I have a friend Bless her heart. Every time she goes to the store she will buy me something. Like gluten-free crackers, or something. I tell her "Don't buy me this stuff!"  "I didn't eat it before going gluten-free I won't eat it now" I try to explain to her I am eating more natural foods instead of processed. Something that is hard for her to wrap her head around :) It's ok she is just trying to help or support me. I took all the crackers to my daughters , I made a cheese and meat tray and took the crackers :) It's all good! 

People always ask me "so when can you start eating regular?" I say If you mean by regular your talking Gluten , I can never eat it.. It is damaging to my body ... I cannot ever eat it... 

notme Experienced

I tried to tell her about how miserable I was with my daily headaches for 12 years, and when that switched to daily migraines in January. Her response: "well, everyone has headaches." (in a tone of voice that implied that I'm a hypochondriac).

nope - everyone does *not* have headaches - i used to think that, too, because i had constant headaches.  then, poof, it went away after i was gluten free for awhile.  i didn't even realize that i had a continual, dull headache until it finally left  :)  she is your sister?  chances of her having symptoms are pretty high, she may even be afraid of the whole celiac thing...

 

i am right now headache free and i can't remember the last time i have had one.  (probably a few months ago and it was created by krazy hormones - explainable and short lived)  i take, like, 1 pain reliever every 2 months on average (1 ibuprofen tablet)  that is like a record :D

Auntie-Manda Apprentice

Same for me! I will be 27 this month, and I have had a DAILY headache since middle school at least. Maybe sooner- I can't remember. I just remember taking excedrin regularily in middle school. I HAD to get help when they changed to daily migraines. Really, it was a month-long migraine that was better or worse depending on the day. I could hardly function. At times I couldn't function. I said good bye to gluten, and they disappeared almost immediately. I've lost 40 lbs, and I have ENERGY, and MOTIVATION now. This is definitely working out for me! Yes, she's my sister. I'd love to talk to her seriously about it, but she thinks it's a load of crap. You just can't change someone's mind when they have already decided what they're going to think. I AM making progress on convincing my mom to try gluten-free and see if it helps some of her symptoms. I worry about her because she doesn't have health insurance, and if her body is being damaged, it will cost a LOT to fix it someday.

madminx Rookie

Thanks for the replies everyone! 

I think I'm going to stop talking to them about it, unless they specifically ask about it, or if it's unavoidable (like when going out to eat with them). 

I finally have an appointment tomorrow with the doctor so hopefully I will get some definite answers soon. 

misschris84 Newbie

I wish you luck with your friends. I was diagnosed less than 2 months ago & I cant get my family to understand the severity of the situation. My husband has his moments... it makes me feel kinda depressed to say the least.

You are not alone, hang in there

cyclinglady Grand Master

I wish you luck with your friends. I was diagnosed less than 2 months ago & I cant get my family to understand the severity of the situation. My husband has his moments... it makes me feel kinda depressed to say the least.

You are not alone, hang in there

Welcome Miss Chris!

 

It is hard to have celiac disease and it can be depressing!  I was diagnosed in March.  Fortunately, my husband's been gluten-free for 12 years.  Who would have thought that both of us would have issues with gluten?  Even though I was already gluten-free savvy, I took my diagnosis hard.  But six months later, I'm feeling pretty good thanks to the support of this forum.  

 

I admit it has been hard for family and friends to get "it".  But, slowly they are coming around.  

 

So, when you need some support, feel free to talk to some new friends (ones that have been walking in your shoes!)  And that goes for everyone!

 

Have a great weekend!  

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Xravith posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Challenges eating gluten before biopsy

    2. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      16

      My only proof

    3. - Dakota01 commented on Scott Adams's article in Winter 2026 Issue
      1

      Are Gluten-Free Processed Foods Making You Sick? (+Video)

    4. - JoJo0611 posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      0

      Awaiting Biopsy results


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,456
    • Most Online (within 30 mins)
      7,748

    Lecina
    Newest Member
    Lecina
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Xravith
      Hello, I'm back with a second post. The first time I wrote, I mentioned the possibility that my symptoms were related to gluten. I did a genetic test in which I resulted to have the predisposition, but the results of my blood test were all negative without IgA deficiency. My doctor suggested that it was necessary to do a biopsy to rule out Celiac Disease. However, he said, because of my family history and my symptoms were strongly related to gluten, it was very possible that my Celiac Disease is developing and my antibodies may become positive in the future.  I tried to continue the gluten challenge for the biopsy, around 2-3 g of gluten per day, but it was enough to make me feel worse each passing day. I started developing anemia and other mild nutritional deficiencies, and it was really affecting my daily life. I'm a student and exams are coming up, so my doctor suggests me to strictly remove gluten until I feel better so I could study without problems until I could do the gluten challenge when I come back home for holidays. Since going gluten free, I feel like a completely different person. My mind is clearer, I have no stomach pain during the day, and even my nails improved within just two weeks. It could also be Non-Celiac Gluten Sensitivity, but of course I’ll need the biopsy to know for sure. I was wondering, has anyone else had negative blood tests at first and later tested positive? And has anyone struggled with the gluten challenge because of symptoms?
    • Jmartes71
      Doterra is a life saver and yes I feel like im waiting because Im getting yes you are celiac, no your not celiac. Im so FRUSTRATED, exhausted and tired of explaining to medical why I feel this way.Im stressed because my body isn't feeling well.Yes I am and no it's not just a food allergy as downplayed with doctors Ive seen.I even went to the " celiac  specialist " Dr Fernandez-Becker who down played my ailments and stated im not and then yes I am I even had one her " care team" ask my why do you want that diagnosis. UNMMMMM. I don't want it, its been my life confirmed in 1994.Menopause intensified extra sensitivity and medical has down played my sibo, ibs, CELIAC, now im having skin and eye issues. I thought help was available but its been a complete medical disaster. 
    • JoJo0611
      I have had my endoscopy this morning with biopsies. My consultant said that it looked like I did have coeliac disease from what he could see. I now have to wait 3 weeks for the biopsy results. Do I continue eating gluten till my follow appointment in three weeks.  
    • cristiana
      Hi @emzie and welcome to the forum. Perhaps could be residual inflammation and bloating that is causing sensitivity in that area.  I was diagnosed with coeliac disease in 2013 and I remember some years ago my sister telling me around that time that she had a lady in her church, also a coeliac, who  had real pain when she turned her torso in a certain direction whilst doing exercises, but otherwise was responding well to the gluten-free diet. As far as I know is still the picture of health. I often end up with pain in various parts of my gut if I eat too much rich food or certain types of fibre (for some reasons walnuts make my gut hurt, and rice cakes!) and and as a rule, the pain usually hangs around for a number of days, maybe up to a week.   When I bend over or turn, I can feel it.  I think this is actually due to my other diagnosis of IBS, for years I thought I had a rumbling appendix but I think it must have just been IBS.  Reading the experiences of other sufferers, it seems quite typical.  Sensitized gut, build up of gas - it stands to reason that the extra pressure of turning can increase the pain. When I am glutened I get a burning, gnawing pain in my stomach on and off for some days - it isn't constant, but it can take up a few hours of the day.  I believe this to be gastritis, but it seems to hurt irrespective of movement.   Anyway, you are doing the right thing to seek a professional opinion, though, so do let us know how you get on.   Meanwhile, might I suggest you drink peppermint tea, or try slices of fresh ginger in hot water? A lot of IBS sufferers say the former is very helpful in relieving cramps, etc, and the latter is very soothing on the stomach. Cristiana
    • emzie
      Hi! One of the usual symptoms I have with a gluten flare up has deviated a bit and I thought I'd search for advice/opinions here. Also to see if anyone goes through similar stuff. Monday all of a sudden I got really bad pain in my stomach (centre, right under the chest, where the duodenum would be located). I ended up having to throw up for 2 hours, my body was trying to get rid of something from all sides and it was just horrible. Since then I havent been nauseous anymore at all, but the pain has stayed and it always worsens the moment i start moving. The more I move the more it hurts, and when i rest longer it seems to dissapear (no movement). I've had this before, but years ago I think around when I first got diagnosed with coeliac, where each time I moved, my stomach would hurt, to the point where I went to the ER because doctors got freaked out. That only lasted 1 night though, and Now it's already wednesday, so 3 days since then, but the pain persists and remains leveled. it doesn't get crazy intense, but it's still uncomfortable to the point I cant really go out because Im afraid itll turn into a giant flare up again. I couldn't think of where I could possibly have been glutened at this bad of a level and why it hasn't passed yet. I went to the GP, and as long as I have no fever and the pain isnt insane then its fine which I havent had yet. Tomorrow im also seeing a gastroenterologist specialized in IBS and coeliac for the first time finally in years, but I thought I'd ask on here anyway because it still hasnt dissapeared. It also hurts when someone presses on it. Maybe it's just really inflamed/irritated. I'm just frustrated because I'm missing out on my uni lectures and I do a sports bachelor, so I can't get behind on stuff & next to that i'm also going to go to the beach with my boyfriend's family this weekend: ( 
×
×
  • 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.