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 Are The True Risks Of Eating Gluten?


Magnus

Recommended Posts

Emme999 Enthusiast
You *will* become more sensitive as your gut heals. If you look at the mechanics of the condition, a Celiac who consumes gluten regularly has suffered extensive damage to the absorptive layer of the small intestine. The surface area drops by over a factor of 100. So, consequently, you absorb less gluten if you continue on an untreated track, and you have less of a response. Also, the destruction to the absorptive surface occurs MUCH more rapidly than the healing process. If you Glutenate yourself once a month, you are actually moving backward, not forward.

Now, when your gut starts healing, your absorptive area increases exponentially. So, you have a much easier time absorbing the poison. Hence, your reactions become quite pronoounced. -P

Well I'll be damned :blink:

I had been wondering about the whole reaction deal. Until I was consuming gluten in vast quanitities (gluten challenge) I didn't have any reactions to gluten (well - that I was aware of anyway!).

My gastro doctor said that my villi looked "flat" so ... now it's all coming together ;)

Thanks for educating me!!

- Michelle :wub:


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



Celiac.com Sponsor (A8-M):



  • Replies 102
  • Created
  • Last Reply
lovegrov Collaborator

"You *will* become more sensitive as your gut heals."

This simply is not true for everybody. I've been gluten-free for more than three years and have not become more sensitive at all. I know others who are the same.

richard

westiepaws Apprentice

Hi! I have wondered the same thing you are wondering. When I was diagnosed, I didn't think I had ANY symptoms of celiac! I ONLY got tested because my mom was diagnosed!!!

Yeah, I knew I was fatigued, but having been a spousal caregiver for 3 years and widowed for 1 1/2, I chalked the fatigue up to that. I went on the diet somewhat begrudgingly.

WELL -- after I went on the celiac diet, my abdomen was flat again -- the celiac had been causing it to pooch out every afternoon!! My GI tract was calmer, fewer oddities and pain going on with the colon.

(Remember, *****I DIDN"T THINK I HAD ANY SYMPTOMS OF CELIAC AT ALL**** when I got tested -- I thought all that GI stuff I experienced, the pain, distension, etc., was just part and parcel of getting older. I'm 38.)

My energy level has improved incredibly, as has my mood. I have lost 10 of the about 25 extra pounds I had gained over the last 4 years (this is a good thing). My hair is shiny, not dry and frizzy -- this is happening from the base of the new hairs coming in, so it is not related to any hair products.

My nails are strong for the first time in my entire LIFE.

And probably the most amazing thing, my rosacea (facial redness/acne in adults) is almost GONE. I mean, GONE. And THAT is supposed to be an INCURABLE disease. I am comfortable enough for the first time in my adult life to not wear make-up all the time. (I saw improvement from the diet re: my skin, but an important factor, as well, was throwing out soaps, shampoos, etc., that contained gluten, soy and dairy. You would not believe how many personal hygiene products contain them -- everyone is marketing the "natural ingredient" aspect of their products.)

Now if I accidentally eat some gluten (or soy or dairy, as I'm allergic to all three) I KNOW it. Fatigue, GI problems, and I start getting itchy and breaking out and don't sleep well. I usually develop a bad mood, too! :blink:

I actually eat much healthier than I ever did pre-diet. That's in part because the three things I'm allergic to permeate prepared, pre-packaged foods, so I pretty much just eat healthy, real food. And I DEFINITELY indulge in allergy-free brownies and a cranberry sort of cobbler that are fast-n-easy, so I don't feel deprived. And for some reason, I really enjoy my food now and I want to share with others. For example, last week I fixed a gluten, soy and dairy-free meal one night for four girlfriends, along with a gluten/soy/dairy-free cake for the birthday girl who attended! They were all raving about the food, and took the leftover slices of cake home to their sweeties.

So, it's not so bad. Life is what you make it. I mean, after what I went through w/my husband's illness and losing him to death at 37 -- this diet is a freakin' piece of cake, you know? It's also a piece of cake compared to what my mom's dealing with, as a result of not being diagnosed as celiac until she was 64 years old.

My mom did not get diagnosed until she was 64 and she's got osteoperosis, fibromyalgia, neuralgia, irritable bowel, has had chronic depression all her life, has been anemic most of her whole life, along with a host of other stuff.

Continuing to eat gluten and anything else you are allergic to, as my mom did unknowingly for 64 years, can make your elder years a total nightmare. If you think $500 is expensive for one doctor visit, you should see my mom's medical expenses. The older she gets, the earlier she meets the limit at which her medical insurance is paying 100 percent. I am not kidding!

The other thing about medical expenses associated with diagnosis, etc., is that they are a bit at first, but they drop once you are diagnosed and they check your genetics, etc. I only go in once every 3 mos. to see my endocrinologist, and just got released to once every 3 mos. to see my nutritionist. That is nothing compared to my mom's expenses for treating all her celiac-induced health problems.

Okay, I've rambled on enough. You may want to find another celiac-friendly dr. in your area and maybe compare prices. Check with www.celiac.org or some other sites to see if they can give you recommendations of drs. in your area online, or by phone.

Hugs,

westiepaws

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,549
    • Most Online (within 30 mins)
      7,748

    Trina Morrow
    Newest Member
    Trina Morrow
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Thanks for the update @TerryinCO! Would you elaborate what you mean when you say your genetic tests show that you are "10x higher" for developing celiac disease? 10x higher than what? There are two main genes, HLA-DQ2 and HLA-DQ8, that have been identified as providing the potential for developing celiac disease. Since 40% of the population carries one or both of these genes but only 1% of the population actually develops celiac disease, the genetic test cannot be used to diagnose celiac disease, simply to establish the potential for developing it. Gene testing is usually done to rule out celiac disease vs. NCGS (Non Celiac Gluten Sensitivity). In other words, if gluten consumption is definitely causing someone problems but they don't have the genetic potential for developing celiac disease then the diagnosis would be NCGS. We also know that having both DQ2 and DQ8 puts one at higher risk for developing celiac disease than having just one or the other. But I'm not sure I've ever seen it quantified as in "10x higher". Not sure what you mean by this.
    • Jordan23
      I would stop Xanax. It will eat away at your DAO enzymes needed to break down histamine . No energy drinks will do the same. I use to have all reactions in stomach now it's changed and started in my chest , which completely sucks and bummed. Maybe your reacting to high histamine foods. But it's hard to avoid cross contamination.  I would get pea milk made by ripples .it's a blue bottle . Ru getting cross reactions? Corn gets me. If it says gluten free it's probably not. Nibble at new foods and wait for reactions. Could be sudden or take 2 hours but some people think it hits 2 days later no way. Avoid coffee. Stick to free range chicken and steak or fish . Do lentils package by kroger works for me it doesn't even say gluten free but works for me just rinse well. Make big soups with sweet potatoes, cauliflower,  brocoli,  cucumbers, and add lentils or cook lentils separate taste better. If you can do potatoes add those inn huge plus. If you can do dairy yogurt try Noosa or a certified gluten free one. Don't smoke I had to quit creates heat and acid in your stomach which lowers your vitamins to break food down. Your reactions are in your chest . Do smoothies everymorning with apple.  🥒 cucumbers, arugula , oranges or add what you can tolerate with water. Try a peppermint tea certified gluten free that works for you. Watch out for spices like turmeric they add flour fillers to prevent caring. I got hit hard by that.  If you have a huge attack get the pin or eat oranges quick. If quinoa works for you get certified huge plus. I could go on and on . Just nibble first wait and see then continue eating it.  It's hard to find nuts that work for you. Maybe try nuts.com..... enter with caution
    • TerryinCO
      I haven't been on the site for a while and I have some update info.   Genetic tests show I have the Celiac markers and high risk for Celiacs's  (10X it shows).  Immoglobulin A and G are low - just below the 'green' range; immoglobulin M is in the 'green'.  Zinc, Iron, magnesium, ferritin, and b12 are all in the 'green' range. I've been off the PPI for two weeks now and no real problems...minor heart burn and OTC antacids fix that.  So that's good to be off of that for good. I switched to a b complex sub lingual vitamin. I was surprised about the genetic results on Celiac markers. To my knowledge no one in my family had it or were diagnosed with it.  But they could have had and never been diagnosed.  And at 76 this has come up for me. Gluten free diet is going well and I do feel better on it - nothing major in changes - just better. I appreciate all the advice I've gotten on this site - lots of experience knowledge to draw on here. So thank you, all.
    • ALBANICKAP
      Thank you Scott, I will try what u suggested. 
    • pplewis3d
      Does anyone know if Citracal Petites supplements for Calcium and Vitamin D3 are gluten free?
×
×
  • Create New...