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

Newly Diagnosed- How To Explain It To People


Trachellium

Recommended Posts

Trachellium Newbie

Hi there-

I hope this doesn't come across as ignorant, I am still learning all about this but in the meantime am finding it a little hard to explain to people. I mean I recognize it as a disease but I feel like the word disease freaks people out (and maybe I just shouldn't care as much about freaking people out). But I also don't want to discount it because I realize it is much more than just a gluten allergy. Of course I will go in depth about it with close friends and family and refer them to websites, etc., but what about coworkers, people in restaurants and grocery stores, etc.? Does severe gluten intolerance suffice? Do any of you have any good phrases that succinctly help convey the basics of the disease? Thanks so much. :D


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



Celiac.com Sponsor (A8-M):



ksymonds84 Enthusiast
Hi there-

I hope this doesn't come across as ignorant, I am still learning all about this but in the meantime am finding it a little hard to explain to people. I mean I recognize it as a disease but I feel like the word disease freaks people out (and maybe I just shouldn't care as much about freaking people out). But I also don't want to discount it because I realize it is much more than just a gluten allergy. Of course I will go in depth about it with close friends and family and refer them to websites, etc., but what about coworkers, people in restaurants and grocery stores, etc.? Does severe gluten intolerance suffice? Do any of you have any good phrases that succinctly help convey the basics of the disease? Thanks so much. :D

There's no such thing as an ignorant question here! My doctor interchangeably calls me either celiac or gluten intolerant. I choose to explain myself as simply gluten intolerant because I think people understand that more. If I say I am celiac, alot of times I will get "what is that?" compared to gluten intolerance. With restaurants, I usually say I am gluten intolerant and will get very sick if I ingest wheat, barley, rye, and probably oats. I am self employeed and my staff witnessed me losing tons of weight (my clothes were seriously hanging on me) always tired, and spending a lot of time in the loo (thank goodness only office gals noticed this one!) Don't know what you do for a living but say you worked in an office, you may only need to say something if they bring in outside goodies to share etc. Its really up to you how much information you give them. You are right to include close friends and family because they can be your greatest support system. Celiac is a very serious auto immune disorder and I take it seriously but I stay positive when explaining it to those that want to know...as long as I am strict with the diet...I am not sick and feel the best I've felt in over 20 years! Welcome to the forum!

Mother of Jibril Enthusiast

Welcome to the group!

I've been off gluten for three months now, but I'm still working on this.

Honestly, I don't go out to eat very much. It's so hard to find things that don't have gluten, dairy, or corn <_< Plus I'm getting more and more sensitive to cross-contamination. Ugh. After I was glutened by some french fries (at a place where the only thing they deep fry is french fries) I decided it just wasn't worth it to take a chance. So... I try to stick to basic things like salad, meat, eggs, and drinks (coffee, tea, etc...). I also tell people that I can't eat anything with wheat because it will make me very sick. IMO, you don't have to be more specific than that. Rye, barley, and oats are also forbidden, but I figure the average waiter/waitress is not going to have a CLUE if the food has those ingredients.

I stopped eating pork products 15 years ago for spiritual reasons and I'm really good about checking menus, but every couple of years I manage to bite into something that has bacon or ham. Mistakes happen. People get busy and they do things like, "Oops... forgot you didn't want bacon bits on your spinach salad... I'll just scoop them off." With gluten that is just NOT acceptable. Take a close look at your food when it arrives (before you take a bite!) and don't be afraid to send it back if you think there's a problem. And don't forget about the bread... either ask them to leave it off or put it on a separate plate.

Most of my co-workers are jerks :angry: I don't even try to explain. I'm also not forced to eat with them, so it's really no big deal.

Friends and family are a different story, especially family... because my celiac and gluten-sensitive genes had to come from somewhere! I give them as much information as they're willing to listen to, emphasizing how GOOD I feel being off gluten, dairy, and corn :)

kimis Collaborator

I just carry a Rice Chex box around with me. If someone needs a further explaination, I just hand them the box and tell them to read the side panel.

ShayFL Enthusiast

A lot of peeps dont even know what "gluten" is. So be prepared.

I now just say gluten intolerant. It sums it up either way. I cannot eat gluten.

kbtoyssni Contributor

I usually say I have a gluten allergy so I can't eat wheat, barley, rye or oats. Allergy is a well-understood term so for waiters I don't think it matters if it's not technically correct. I don't need to get into the type of reaction my body has to gluten with a waiter; all they need to know is that I can't eat it. For people I know better or those who ask questions I start talking about the fact that it's actually autoimmune, etc.

sbj Rookie
am finding it a little hard to explain to people. I mean I recognize it as a disease but I feel like the word disease freaks people out ... I also don't want to discount it because I realize it is much more than just a gluten allergy. ... what about coworkers, people in restaurants and grocery stores, etc.?
I've had the same issues. It feels odd to have to get all wordy with people and explain it. It also feels strange to say 'disease.' Eyes tend to grow large and people take a step backwards! But I am sooo tired of responses like, "Oh - so you're allergic to wheat."

Lately I am leaning towards:

"I have an autoimmune disorder called celiac sprue. If I eat wheat or anything with flour - like that office birthday cake - then my small intestine gets damaged."

Rice Chex (I have some here at work):

"Celiac disease is a multi-system, multi-symptom autoimmune disorder that is triggered by gluten, a natural protein found in wheat, barley, and rye."


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



Celiac.com Sponsor (A8-M):



*Daniella* Apprentice

Hello! I'm new to this celiac thing too. Tomorrow will be my 1 month anniversary.

What an excellent question. I'm having the same problem. When I try to descibe my situation people either shut down or don't care. One of my co-workers yesterday asked me if I was still on the diet. UMMM YES! FOREVER! I've sort of decided not to mention it until somebody asks why I'm eating the PB&J on a rice cake. Haha!

Tallforagirl Rookie

I was out at a restuarant yesterday, and the waitress, who claimed to know all about Celiac disease, asked me "how much gluten free are you - point 4 or point 7?" I have not the faintest idea where she got the idea that gluten intolerance can be measured in percentage points.

I ended up choosing a salad and garlic prawns, after confirming all ingredients.

Unfortunately this was my first date with a new guy. I really should have known better than to go for a meal on the first date. It was sooo embarassing. He thought that since the restaurant obviously didn't understand my needs, there was a good chance I might poop myself halfway home.

I quit, I don't want to do this anymore. :angry:

NorthernElf Enthusiast

I say I have celiacs and that gluten makes me feel like I have a combination of a hangover and the flu. No fun.

I have found that saying gluten intolerance makes folks think I can still have some gluten - like some folks with lactose intolerance can get away with certain milk products in small amounts.

FWIW, I never got a diagnosis because I went gluten free too soon for accurate testing. For awhile I felt silly saying I had celiacs since I never had a paper with a positive test...however, even small amounts of gluten affect me so I don't care anymore !!!

ang1e0251 Contributor

I have come to say in restaurants "I have some severe food allergies and can't let even a crumb of bread touch my food or I'll have a reaction". They get this kind of wording and it sounds kind of mysterious to them since it isn't completely specific. I know it isn't accurate but it's a restaurant and the important thing is not to get sick.

If people make a comment or a "wow, you can't eat anything", I just give an "oh well" shrug. No further explanation is necesary to strangers.

I would call ahead to the caterer but I wouldn't depend that she won't make mistakes. Take some backup food or eat before you go. I've been hungry at those events and it's no fun.

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. - xxnonamexx replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      My journey is it gluten or fiber?

    2. - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    3. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    4. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      My journey is it gluten or fiber?

    5. - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,696
    • Most Online (within 30 mins)
      7,748

    Knotalota
    Newest Member
    Knotalota
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • xxnonamexx
      I read that as well but I saw the Certified Gluten free symbol that is the reason I ourchased it.
    • cristiana
      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac.  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
×
×
  • 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.