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

New To This Forum, Gf Since 3/04


keenpetite

Recommended Posts

keenpetite Newbie

I was diagnosed after suffering for over 15 yrs with severe digestive problems & a rash on both arms. My worst enemies are wheat, corn, oats, beef, peanuts, dairy. I suspected Celiac 3/90, went to a MD only to be told "You're not anemic, so you it can't be Celiac Sprue". At this time I was going thru severe bouts of digestive problems. Extreme widespread bodily pain began soon after, sent to rehumatologist & was told I had Fibromyalgia, sleepless nights, fatigue plus became my costant companions.

Fast forward to 3/04 a new pcp suspected food allergies & after 18 days on a elimination diet & reintroducing a new food every few days we were finally able to pinpoint the true culprits.Rash has cleared up very well. A few problems continue. Happy to report I've been gluten-free since then & do not miss any of the forbidden fruits (pun intended ) lol

Please, I'd like to know, anyone, when a non gluten-free food is ingested is there any severe bodily pain within 10-15 minutes?

Any info is greatly appreciated.

I've been able to find quite a few delicious gluten-free recipes that I'm literally having a ball with.

My best regards to all,

keenpetite :o


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



Celiac.com Sponsor (A8-M):



Merika Contributor

Hi and welcome,

Everyone's reaction to non gluten-free foods is different, and pain in 15 minutes seems like it could indeed be possible.

Merika

KaitiUSA Enthusiast

As said in the previous post...everyones reactions are different.

I do not get pain..I get nausea and I can usually tell right away. My reactions last about 2 weeks and the 7th day is usually the worst.

Wow in 90 your doctor told you since you weren't anemic you didn't have celiac...sounds like the typical doctor. Not everyone even gets symptoms and there are over 200 symptoms so not everyone would even get the same ones. I feel bad for the celiacs back then because I know now it's still very hard and technology and foods and just everything has advanced so I can't imagine how hard it was then. Finally celiac is starting to be discovered more by doctors and the general public so maybe people won't have to go what we went through in the future.

pixiegirl Enthusiast

I get pain when I ingest gluten and mine starts about 20 minutes after eating gluten, but its at its worst the following day. I had a lot of your symptoms... fatigue, I've been diagnosed with Chronic Fatigue Syndrome and I'm not sure I ever had that, I'm almost symptom free as long as I stay away from gluten. I have various rashes and had years of sleepless nights.

Best to you! Susan

ianm Apprentice

Most doctors are idiots when it comes to this disease. I was not anemic, I was very overweight before I found out what the problem was. I don't experience pain but whenever I get glutened I don't always get the same reaction. I usually feel fatigue and brain fog but the last time my guts were churning a bit.

I have found so many new and better foods to eat on a gluten-free diet that I just don't miss the things I used to eat.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,218
    • Most Online (within 30 mins)
      7,748

    JTaylor
    Newest Member
    JTaylor
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      @sillyyak52, If it makes you feel any better, I have a sibling who thinks the dinner table (at fine dining restaurants, and less formal pub grub settings etc.) is a personal buffet table and dips into the food of whoever is sitting beside or opposite to them just to get a taste (no plate is safe!) ... never asks for permission ... and has no consideration of gluten cross contamination even though I've explained it diplomatically with articles, pictures of dermatitis herpetiformis (which I've had for years) like @knitty kitty and I both suggest you do. I avoid that sibling at restaurants now and sit at the opposite end of the table out of arms reach! I've had similar treatment at a recent siblings 60th BBQ with family and friends (brought my own food and burger), where I was told (in a very rude manner) "tough luck, there's nowhere safe ... just cook your burger on the BBQ" which was cross contaminated ... I stood my ground and asked for a clean frying pan to cook my burger safely and separately. 
    • Deanne jones
    • trents
      knitty kitty makes a good point. Avocados are high in histamines. So are bananas. Both also trigger histamine production in the body when consumed so there's a double whammy with those two foods for those struggling with histamine intolerance/MCAS
    • knitty kitty
      @Sharke, The updated guidelines for a gluten challenge are to eat ten grams of gluten per day for two weeks minimum.  Lesser amounts of gluten (3 grams) don't provoke an immune response strong enough that the antibodies leave the gastrointestinal tract and get into the blood where they can be measured in tTg blood tests.   Have no doubt that the antibodies made in the small intestine are doing damage there, even if you don't suffer severe symptoms, yet. Did you react to barley prior to going gluten free? Have you been checked for chronic autoimmune gastritis which is another autoimmune disease that sometimes occurs with Celiac Disease? Have you been checked for nutritional deficiencies?  Thiamine deficiency (Gastrointestinal Beriberi) can cause constipation and/or diarrhea, abdominal pain, and weight loss.   Thiamine Deficiency Disorders https://pmc.ncbi.nlm.nih.gov/articles/PMC8451766/  
    • knitty kitty
      @sillyyak52, Count another one in the same boat!  My family has always been in denial.  They said my tummy aches were a ploy to miss school.  My parents passed from health problems associated with uncontrolled Celiac Disease (Abdominal Aortic Aneurysm and Glioblastoma brain tumor).  My sister still has her head buried in the sand.   I agree with @Rogol72, try the consequences of untreated celiac disease shock treatment.  Sometimes people are just scared of having to change their comfortable lifestyle.
×
×
  • Create New...