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

Need Your Input


Sabina

Recommended Posts

Sabina Newbie

I am wondering what you, more experienced persons think about this. I am worried about both of my kids. I have been tested for celiac disease after being gluten-free for 3 1/2 years with a short ( probably too short) gluten challenge of about 4 weeks where I did not eat as much gluten as I probably should have. My results came back highly positive for the anti-gliadin antibodies (IGG) but inconclusive, still within normal for the other 2 blood tests. Obviously I feel much better gluten-free and my symptoms resolve also. My lactose intolerance and acid reflux both completely disappeared on a gluten-free diet.

I primarily got tested because both of my children have a lot of stomach complaints. My oldest child suddenly became very heavy as a teenager and then lost a lot of weight fairly suddenly. Now , in her 20's,she is extremely thin, tired and cold all the time, and consumes truly astounding quantities of food without gaining any weight. I cannot describe how much she eats -it has to be seen to be believed. She is also lactose intolerant and is in her 20's. She is not bulimic.

My other daughter eats next to nothing and is slim and complains of nausea and bloating on an almost daily basis.

We are of Irish descent ( the western part) and are 2nd generation Americans.

Does anyone know of relatives with symptoms such as this and should I be concerned that they have undiagnosed celiac disease?

Also - has anyone ever read of a connection between celiac disease and atrial fibrillation? ( I ask this question on my father's behalf)

Thanks for any help!


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



Celiac.com Sponsor (A8-M):



Guest aramgard

Your family all needs to be tested, and probably needs to stay gluten free. You might also try adding electrolytes to your diet for the rapid heart beat. Before I was diagnosed I often had episodes of rapid heart beat and after I added a banana and some extra electrolytes to my diet --and going gluten free, I rarely had a problem. Shirley

seeking-wholeness Explorer

Sabina,

Your children sound like my sister and me! When I was in high school and college, I had very little appetite and weighed less than 100 pounds (I am 5'5" tall), but despite my pediatrician's concerns, I did not have an eating disorder. My younger sister, however, was quite pudgy until she hit adolescence, when she suddenly stopped gaining weight and may even have lost some during her growth spurt. Now, she is quite willowy herself.

After college, on the other hand, I ballooned to 150 pounds (BEFORE my first pregnancy)! I managed to drop the excess weight after each pregnancy, and now I weigh a relatively ideal 115 pounds (I am small-boned even though I am tall). Before I went gluten-free, though, I was always tired, cold, and ravenous. People tried to blame my hunger on breastfeeding, but although that accounts for some of it, I don't find it a satisfactory explanation for why I had to consume four meals and two snacks every day just to keep going (and often had to get up at night to forage some more)! It got to the point where I realized that if I ever felt full but not bloated, that was my cue to get up and fix some more food, because fifteen minutes later I would be dying of starvation!

I have told my family a bit about celiac disease and that they should be tested, but I'm not sure any of them will follow through. I wish they would, though! It would be great if your relatives would get themselves checked out.

I seem to remember that nutritional deficits and electrolyte imbalances can cause heart rhythm abnormalities, and celiac disease could certainly be the underlying cause of these conditions. Your father should definitely be tested, as well.

Good luck to you and your family as you seek a diagnosis!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,191
    • Most Online (within 30 mins)
      7,748

    Beatle Jane
    Newest Member
    Beatle Jane
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • WednesdayAddams13
      Hello,   I contacted the makers of Alpine Original Spiced Cider Drink Mix and they sent me this email.....   Subject: [EXTERNAL] Fw: Ref. ID:1335211 Alpine Original Spiced Cider Drink Mix.               On Friday, December 6, 2024, 1:04 PM, Consumer <baking@continentalmills.com> wrote: December 06, 2024   Dear Janie, Thank you for taking the time to contact us regarding our Alpine Original Spiced Cider Drink Mix. We appreciate your interest and are happy to provide you with additional information. This product does not contain gluten. However, it is not manufactured in a gluten free facility. If I can be of further help, please contact me at 1 (800) 457-7744, weekdays 7:00 a.m. to 4:00 p.m. (PT), or visit www.alpinecider.com and select "Contact Us." Sincerely, Kristin Kristin Consumer Relations Specialist Ref # 1335211   I hope this helps everyone.  I am currently looking for a spiced hot apple cider drink and have yet to find one that is not made in a plant that manufactures other gluten products.  It's so frustrating. 
    • trents
      @Rogol72, dermatitis herpetiformis occurs in a minority of celiac patients and if the OP hasn't developed it yet I doubt it will show up in the future. I think it unwise to use a scare tactic that probably won't materialize in the OP's experience. It has a good chance of backfiring and having the opposite effect.
    • Rogol72
      Hi @trents, You're correct. The OP mentioned fatigue and vitamin deficiencies as the only symptoms at the time of diagnosis. Since the family are not taking him/her seriously and find them to be too fussy, I suggested showing them pictures of dermatitis herpetiformis as one of the consequences of not taking the gluten-free diet seriously ... would make life easier for him/her, and the family might begin to take his/her strict gluten-free diet more seriously. A picture says a thousand words and the shock factor of dermatitis herpetiformis blisters might have the desired effect. The OP did say ... "How do you deal with people close to you who just refuse to understand? Are there any resources anyone could recommend for families that are short and easy to read?".  @sillyyak52, It might also help mentioning to your family that Coeliac Disease is genetic and runs in families. Any one of them could develop it in the future if they have the HLA DQ 2.5 gene. Here's a Mayo Clinic study calling for screening of family members of Coeliacs ... https://newsnetwork.mayoclinic.org/discussion/mayo-clinic-minute-celiac-disease-screening-for-family-members/ https://newsnetwork.mayoclinic.org/discussion/mayo-clinic-study-calls-for-screening-of-family-members-of-celiac-disease-patients/ I got glutened a few months ago because I missed the may contains statement on a tub of red pesto. It was my own fault but it happens.
    • peg
      Thank you, Scott!  This is just what I needed.  Appreciate your site very much and all of your time and energy that goes into it! Kind Regards, Peg
    • Hopeful1950
      Oh yes.  I would never recommend taking it for an extended period of time.  When 70% of my body was covered in blistering itchy sores, an amazing doctor prescribed it diagnostically because I was unwilling to do a gluten challenge after already going strictly gluten-free in desperation after 10 years of suffering and being poo pooed by dermatologist after dermatologist. The fact that it stopped the itch and mostly cleared the rash after about 2 months was diagnostic for him.  I stopped it and have remained strictly gluten-free with very few flares since that time (over 10 years ago).  So the fact that it cleared the rash was diagnostic for me.     
×
×
  • Create New...