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

Oh, It's Just The New Thing!


KMMO320

Recommended Posts

KMMO320 Contributor

This is what EVERYONE aside from my sis in law who has celiac disease has said to me. Everyone from my husband, coworkers, my boss (I waitress), friends, family, etc. EVERYONE!

Oh, Gluten is the new bad guy, Dr's tell people it's gluten only because they dont know what it REALLY is. How can wheat cause this. Its just the new thing, its all in your head. The Dr is making you think its Gluten but its not.

And more...

Of course, most times I ignore it..but there are sometime I wonder if I am "going along" with it and believing in the new thing...

The non-support is actually more frustrating than having to eat gluten-free.

Also, everyone tells me its a way for companies to make money off me buying the "expensive food" Actually, all I have bought gluten-free so far are donuts...otherwise, I stocked my house full of just naturally gluten-free foods..

My sis in law who is Celiac has even said that only about 2%of her weekly shopping is on gluten-free foods..everything else she buys is just normal, naturally gluten-free food...

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



dani nero Community Regular

Just give them a small history lesson in celiac. It was discovered ages ago. There's nothing new or "thingie" about it. It's just what it is. If people care less about educating themselves by actually reading rather than just watching silly shows, why should we bugger ourselves over it ;-)

My whole family except for my mom and hubs don't believe me, and I'm still in the process of making myself care less about what they thing.

We need to relax, care less about their "oh so insightful opinions" that come from daily shows, and enjoy our journeys to good health being gluten-free :-)

Link to comment
Share on other sites
mommida Enthusiast

Here's some history. It is believed to be the "wasting away" disease described in the Bible.

The cure was discovered through the starving children of Belgum during the war. Children who had been diagnosed as failure to thrive, became "healthier" when they were STARVING. This lead to the conection ~it was food related. They usually just left the person on a banana diet.

You have to remember there was no "routine" endoscopy in the past. The furthest information gastroenterology had was from Dr. Beaumont. Dr. Beaumont had a patient that was accidentally shot in the stomach. The wound never healed properly and left in layman's terms a "window" into his gut. So Beaumont got to watch human digestion through this window and was termed "the father of gastro physiology"

If this "fad" term is happening because more people are asking to be tested. At least people are hearing about Celiac and DH begging to be tested. Because it matches symptoms that they have had for (what 40 some years depending on their age)?

One out of every 300 people are estimated to have Celiac/ DH. The number is probably higher, because doctors really haven't tested. (It was a blind study of blood supply~ only blood donations were sampled) I always get turned down for being underweight, anemic, and so on. So how are the true bunch of undiagnosed Celiacs going to donate blood? ;)

Sorry went on a Cliff Claven rant. :ph34r: :ph34r:

Link to comment
Share on other sites
bartfull Rising Star

As more and more people hear about it, even if it is through the hype from the famous people who are going gluten-free without needing to, more and more people might put two and two together. If people who actually HAVE Celiac discover it and start eating gluten-free and thereby prevent all of the terrible things that can happen to a Celiac who continues to eat wheat, it is worth it. We who truly have the disease may suffer from the taunts and pooh-poohs of others, but our suffering is nothing compared to the cancer, neurological problems, thydroid problems and the like that an undiagnosed Celiac faces.

Just last night I was talking to a lady I know about it. After hearing the non-digestive symptoms that I have, she now believes her daughter may have it. She has thydroid problems, rashes, and balance problems. I half expect her to show up here in the next day or two. I hope she gets tested, or at least tries gluten-free to see if it helps. I made it a point to direct her to this site so she can learn HOW to go gluten-free - reading labels, CC issues, all the pitfalls that await us in the grocery stores.

Link to comment
Share on other sites
Pegleg84 Collaborator

Yeah, I get a lot of this too. More people are eating gluten free even though they don't have Celiac or an intolerance. I'm not saying it's not healthier to eat gluten free, I just think you're crazy to do it if you don't have to!

I inherited Celiac from both sides of my family. My aunt developed thyroid cancer partially due to undiagnosed celiac. It's definitely not in your head. Also, if eating gluten free makes you feel better, then you should eat gluten-free regardless of any diagnosis.

Just tell your friends/family (as I often do) that the gluten-free diet keeps you a healthier, happier person and they don't want to be around to face the consequences if you get glutened.

Education and awareness helps (how many times have we explained our condition to someone..?), and reminding them that it's a DISEASE, not a fad, and that you wouldn't be doing it if you didn't have to.

Also, if more people eating gluten-free means better/more affordable gluten-free products for the rest of us, all the better.

(though don't get me on a rant about exploiting the celiac. When you're stuck at a restaurant where the only option is a tiny salad, or $5 extra for pizza, what do you think...)

Peg

Link to comment
Share on other sites
1974girl Enthusiast

I was scared it was going to be a passing phase..finding gluten free food in the store. But, my SIL's nephew has autism and has been told to go gluten free. Considering how high the autism rate is, it wouldn't suprise me if they find out it is caused by what we are doing to our food in America! When everything (practically) gets better when gluten free, I think the awareness will just grow...and hopefully the menu! I have friends who do gluten free for their daughter's ticks. Within 3 days they were gone. I am for finding a cure and the University of Chicago says by 2026, they will have one for celiac. However, I wish more studies would be done on how our wheat crop is different than it used to be and maybe stop these other problems as well.

Link to comment
Share on other sites
KMMO320 Contributor

Today's food makes me so.scared and I dont.know.if.its that medical.science is more advanced and thats why they can diagnose more problems, or that our nutrition.is so poor that more problems are arising. Scary times.

Link to comment
Share on other sites

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



Celiac.com Sponsor (A8-M):



JNBunnie1 Community Regular

I have friends who do gluten free for their daughter's ticks. Within 3 days they were gone.

By this I assume you mean nervous tics, not biting ticks?

Just checking....

:ph34r: :ph34r:

Link to comment
Share on other sites
jeanzdyn Apprentice

of course people who have not suffered stomach cramps or chronic diarrhea would think that you are just on a 'fad diet' or something. tell them, in graphic details, about your symptoms!

If you feel better gluten free that is all that really matters!

I want to add that, although some gluten free items are expensive, you can find a lot of gluten free foods that are not any more expensive than any other food items.

I eat a lot less now that I am gluten free, so that $3.50 bag of rice noodles is about 8 meals, and maybe 10 meals, depending on what I have with the rice noodles.

Link to comment
Share on other sites

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      125,024
    • Most Online (within 30 mins)
      7,748

    Patricia Holzworth
    Newest Member
    Patricia Holzworth
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.8k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      Hello, @Kate1990, I reacted to calcium citrate because it's made from oyster shells and I react to seafood.   I chose calcium malate and chelated calcium.  Be sure to take a magnesium supplement as well, but several hours away from calcium.  Magnesium and calcium compete for absorption.  We need calcium for bones, but magnesium and potassium keep calcium in the bones.   Hope this helps!
    • Kate1990
      Hi,   I've started taking calcium citrate supplements from Webber Naturals. It says that it contains no gluten, but not that it is gluten-free. I've reached out to the company by e-mail and they have assured me that it is gluten-free. However, I think I'm reacting to it. I've searched everything else I consume and haven't found any possible source of contamination. I've been looking for other supplement brands that would be certified gluten-free and safe and have found a few options, but none of them ship to Canada. Does anyone know where I could buy calcium citrate supplements (apparently calcium citrate is the one that causes the least constipation, and this is an issue for me). Thanks in advance!
    • Karen Rakhshan
      I am so sorry for your long-term pain and suffering. My symptoms are very similar to yours. Diarrhea for seven years now. Two doctors told me to take Metamucil. It didn’t help. Stomach pain, bloating and terrible nighttime diarrhea got worse and worse. I only stumbled upon Celiac as a possibility through a 23andMe genetic test which indicated I had the genetic marker for it. I went to my GP asking for the test and was told sure - I’ll give you the order, but you probably don’t have it. Guess what?  My blood work was off the charts positive. So high of a number, in fact, that the gastroenterologist I was sent to confirmed me even before a biopsy.  The gastro visit was just last week. I’ve been gluten free for a month now. Small improvement so far, but I’m hoping to continue healing.   
    • Richwhitelady
    • Drewy
×
×
  • Create New...