Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

What Do You Say?


Megan

Recommended Posts

Megan Rookie

My first night gluten free grocery shopping...what fun! I'll share my funny first and then the questions

I visited the Wal-mart bakery last night and just out of curiosity asked if they had anything that was Gluten free, to which the baker replied, "Sure we have lots of things without sugar." I said thanks and then continued my shopping experience...

As we were shopping my beloved boyfriend was just throwing things in the cart and as I've come to realize some brands of the same thing may or may not contain gluten. Like some mashed potato flakes do but Wal-mart brand does not and actually says Gluten free. So I was trying to keep up and read the labels of what he was throwing in and reading the labels of the same product by other companies, because I really do love eggo waffles too and I really do love chips, and tomato soup too! and it was upsetting for him to just be so nonchalantly throwing all these things in to the cart without even stopping to check, and when I did taking off and grabbing more things I couldn't eat. So I started getting upset, and then he was reading labels with me (bless his heart, he was trying on occasion AFTER I got upset, lol) but he was reading them and saying I could have things I couldn't, so I tried explaining...and I got this

"I REALLY THINK YOUR JUST TAKING THIS WAY TOO FAR, JUST EAT SOME OF IT."

ok...

1. it's apparently really not good for my body from a medical standpoint

2. I feel like HELL as soon as I eat aynthing with gluten in it, automatically...I jumped for joy after my first gluten free meal because I felt so wonderful...I didn't swell up to the size of a beachball two minutes after my meal, or halfway in to it, I felt pretty dang good...and I was awake, and more "alert" I think you guys call that fog brain or something...

I think he thinks I'm some sort of hypochondriac... or something... I don't know I mean he's seen my stomach and how I can't hardly function after eating

I'm playing phone tag with two different doctors about this testing thing...I'm terrified to get tested and it be negative because then his support and my families can only get worse. Like I really must just be making it up...especially because within the past year or so I've had some really weird medical problems that have occured for no reason, like a seriously nasty rash, welt, swelling thing on the insides of my ankles that I've gotten the past two summers and not at any other time, that no one can explain and no medication fixes...NOT MY FAULT!!

I finally told him if I complained and whined as much as he did when he doesn't feel well he'd realize I'm not just making this stuff up...

but what do you do?? I have weird symptoms and their stuff other people have on occasion, how do I determine that mine are worse, I get that well i want to nap all the time too, bull...no I don't want to just nap I eat I swell and I fall asleep whether or not I want to...

I'm sorry this is really more of a rant than anything...I just don't get it, how do I make them understand

On a bright note I'm completing my first entirely gluten free day...EVERYTHING is gluten free (watch my Dr finally get ahold of me and send me for testing...uggh eating to be miserable!)

I cannot wait to see how awesome I feel...


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



Celiac.com Sponsor (A8-M):



Lollie Enthusiast

Hi Megan! I think that alot of us have had to deal with the insensitive family/sig. other.....It's crumby, but it seems to be some what normal. I think that if they haven't had to deal with this kind of pain, they don't really get it. I will share with you what I've done with my mom and others in my family. I try to only talk about success with the diet. I only tell them the good and reserve the bad for the message board. Sad but true. Everyone here understands, so I don't have to worry about any one thinking I'm a hypocondriac (sp?). This line of thinking has really helped my situation with my mom. I don't try to explain what I can or can't have, I just take care of myself. I share really good gluten-free stuff I make. I talk about how good I feel now. And I leave it at that.

I would try the positive road and come here when you need to, we all understand!

Lollie

Rusla Enthusiast

I drove the point home by using some medical conditions family members have to get it across. For my brother and his wife (she is diabetic) I said that I would eat gluten for a month if she would go without insulin for the same period of time. For my mother, I told her the same thing only she had to go without her Coumadin for the same length of time. Then they got what it would be for me to eat these foods.

VegasCeliacBuckeye Collaborator

Its amazing how so many family members and close friends suddenly are able to become GI Doctors and Experts on Food Nutrition overnight...They obviously know everything about gluten, the immune system and hos you "feel"...

Some people can be so inconsiderate...

LOL!

:)

gabby Enthusiast

Last time I checked, patient information was confidential...so go ahead and get your testing done. Keep the actual testing and the results to yourself...and only disclose this information if you want to.

It is okay to just tell people you have a health condition and that you have a restricted diet. You do not have to answer any other questions. Just because someone asks you questions about your health, does not automatically mean that they are entitled to an answer. A simple: I'd rather not discuss this right now, is usually enough to change the subject.

Hope this helps, and congrats on your first taste of freedom.

penguin Community Regular

I was with friends this weekend, and as we were eating brunch at this restaurant, one of my good friends said, "well, if gluten is such a big deal, then why weren't you sick all the time?" I said that I was sick all the time for the last three years, and that I was very good at hiding it. Even DH didn't know until I did the testing. She knew I was sick some of the time, but she gave me the three headed look. I think she thought I was going overboard, exaggerating my symptoms, and being a hypochondriac.

Luckily (not for me but it proved my point), I got glutened. I got halfway through my meal and started getting the stoned, face numb thing. Everyone else knew something was wrong almost before I did. I was in a lot of pain by the time we left, so I think she's convinced since she saw it happen :rolleyes:

It sucks that that is what it took, but once your family sees you sick, they'll have a better outlook.

nettiebeads Apprentice
My first night gluten free grocery shopping...what fun! I'll share my funny first and then the questions

I visited the Wal-mart bakery last night and just out of curiosity asked if they had anything that was Gluten free, to which the baker replied, "Sure we have lots of things without sugar." I said thanks and then continued my shopping experience...

I loved it. I'm still laughing after reading all of the rest of your post and responses. I never get over how uneducated people can be. But in the bakery? What do they think makes the bread rise the way it does? Bread fairies???? I was at a conference once and the meal served was chicken alfredo over penne. I said I can't have that, needed something different (before I got my triumph dining cards) and a server came up to me with a plate of the chicken stuff and said that there wasn't any gluten added to the dish. DUH!

If you have the money, you can do enterolab which is supposed to be more accurate than traditional testing. The blood work and endoscopy can have false negatives; way too often for me to consider them reliable. The best and most foolproof testing in my opinion is your own body. I was tested via diet challenge 9 years ago and that's been fine for me and my subsequent drs. (although I did have one internest say I could probably have gluten in small amounts. It was obvious she didn't know a thing about celiac). The diet challenge (which is what you are doing) is a valid diagnostic tool. And as far as other people thinking that you're overreacting - use the poison analogy. Ask them how much arsenic can they have without it being too much? Or just say "I know how I feel with gluten and without gluten." End of story.

But please feel free to come here and vent or ask questions or anything. We understand so very well how much fun it is coping with this disease.

Annette


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



Celiac.com Sponsor (A8-M):



  • 3 weeks later...
eKatherine Apprentice

A funny:

I was explaining to a woman where I was working that I was going to skip the holiday party they threw for the workers because there was no food provided that I could eat, Pizza Hut pizza and supermarket bakery cookies only, as I couldn't eat wheat. She was dumbfounded. She said to me, I could eat the pizza made without the wheat flour, couldn't I? She was fully convinced that some pizza is made with wheat flour and some is not.

cornbread Explorer

Megan, for $99 you can get tested by Enterolab. Open Original Shared Link. The stool test they do is way more sensitive than a blood test that a doctor would do, so, based on your symptoms, it's highly likely you'd get a positive test result.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,198
    • Most Online (within 30 mins)
      7,748

    Jamie0230
    Newest Member
    Jamie0230
    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

    • Scott Adams
      Clearly from what you've said the info on Dailymed is much more up to date than the other site, which hasn't been updated since 2017. The fact that some companies might be repackaging drugs does not mean the info on the ingredients is not correct.
    • RMJ
      To evaluate the TTG antibody result we’d need to know the normal range for that lab.  Labs don’t all use the same units.  However, based on any normal ranges that I’ve seen and the listed result being greater than a number rather than a specific number, I’d say yes, that is high! Higher than the range where the test can give a quantitative result. You got good advice not to change your diet yet.  If you went gluten free your intestines would start to heal, confusing any further testing,
    • Bev in Milw
      Scott is correct….Thank you for catching that!      Direct link for info  of fillers.    http://www.glutenfreedrugs.com/Excipients.htm Link is on 2nd page  of www.glutenfreedrugs.com   Site was started by a pharmacist (or 2) maybe 15-20 yrs ago with LAST updated in  2017.  This makes it’s Drug List so old that it’s no longer relevant. Companies & contacts, along with suppliers &  sources would need to be referenced, same amount effort  as starting with current data on DailyMed      That being said, Excipient List is still be relevant since major changes to product labeling occurred prior ’17.           List is the dictionary that sources the ‘foreign-to-us’ terms used on pharmaceutical labels, terms we need to rule out gluten.    Note on DailyMed INFO— When you look for a specific drug on DailyMed, notice that nearly all of companies (brands/labels) are flagged as a ‘Repackager’… This would seem to suggest the actual ‘pills’ are being mass produced by a limited number of wholesaler suppliers (esp for older meds out of  patent protection.).      If so, multiple repackager-get  bulk shipments  from same supplier will all  be selling identical meds —same formula/fillers. Others repackager-could be switching suppliers  frequently based on cost, or runs both gluten-free & non- items on same lines.  No way to know  without contacting company.     While some I know have  searched pharmacies chasing a specific brand, long-term  solution is to find (or teach) pharmacy staff who’s willing help.    When I got 1st Rx ~8 years ago, I went to Walgreens & said I needed gluten-free.  Walked  out when pharmacist said  ‘How am I supposed  to know…’  (ar least he as honest… ). Walmart pharmacists down the block were ‘No problem!’—Once, they wouldn’t release my Rx, still waiting on gluten-free status from a new supplier. Re: Timeliness of DailyMed info?   A serendipitous conversation with cousin in Mi was unexpectedly reassuring.  She works in office of Perrigo, major products of OTC meds (was 1st to add gluten-free labels).  I TOTALLY lucked out when I asked about her job: “TODAY I trained a new full-time employee to make entries to Daily Med.’  Task had grown to hours a day, time she needed for tasks that couldn’t be delegated….We can only hope majorities of companies are as  conscientious!   For the Newbies…. SOLE  purpose of  fillers (possible gluten) in meds is to  hold the active ingredients together in a doseable form.  Drugs  given by injection or as IV are always gluten-free!  (Sometimes drs can do antibiotics w/ one-time injection rather than 7-10 days of  pills .) Liquid meds (typically for kids)—still read labels, but  could be an a simpler option for some products…
    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
×
×
  • Create New...