Jump to content
  • 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

How Long For Diet


October3

Recommended Posts

October3 Explorer

How long do we need to be gluten free to know if gluten is an issue?

For quick background because I haven't been here in awhile, my 6 yr old has an elevated tTG and chronic recurrent, but mild, anemia. Negative scope. My 8 yr old has frequent tummy aches, gassy and mucousy stools, and chronic inflammation in his esophagus. We're going to start gluten-free Monday for both of them and, as you can imagine if you have children of this age, they are not thrilled about it. We would like to keep the diet for as short a period as possible that will give us clear results. We don't want to have to redo it later. So how long do we go for?


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



Celiac.com Sponsor (A8-M):



WinterSong Community Regular

I've heard that six months is generally an effective length. But I suggest making sure that you really research everything thoroughly before you begin so the switch isn't as hard for them. Get gluten-free snacks, dressings, sauces, ect. Find some easy kid-friendly recipes that are highly rated - maybe have your kids help you cook so they can get involved and begin to see this new way of eating as something fun. Also, pick their favorite foods and find a way to make it gluten-free so they see that they can still have the foods they love.

Best of luck!

eatmeat4good Enthusiast

It must vary greatly from person to person. I had to bribe my son to give me one week gluten free when I suspected that was the problem He ate a pizza after one week and became violently ill. He decided really quickly that he never wants to touch gluten again. He slept 23 hours, nausea, fog, depression, asthma and fatigue for a week afte only having been off it one week. I was off it one week also, then got cross contaminated by not knowing about soy sauce being wheat sauce. I got violently ill and had migraine headache. Both of our food challenges were very short and completely accurate. So you can try for two weeks to a month if you want. Or longer if you want. A friend of mine did 2 weeks with her kids and they also reacted immediately on consuming gluten. Just another perspective. Once it is out of your system, you can have really big reactions on reintroducing. My sis took her kids off for 2 weeks. First gluten meal had 2 of the 5 kids vomiting. Good luck with your decision.

WinterSong Community Regular

Oh wow, I didn't know you could tell after that short of time. Don't listen to my 6 month suggestion then :P

Darn210 Enthusiast

We did a trial run for my son with input/supervision from a pediatric GI. He wanted 6 months.

I think 6 months is fair. Some people show immediate results. Some people don't. Unless you actually show positive results in just a few days, how can you tell which category you fit in? Lack of results in two weeks does not necessarily mean that gluten isn't a problem. It takes a while just to learn to navigate the diet successfully.

October3 Explorer

Wow! 6 months just seems like such a long time to try a diet that I'm not even sure will help at all. Obviously with my 6 yr old having an elevated tTG that points us more to gluten but with my 8 yr old there is no real reason to suspect gluten above all the other things that could be going on. Is the idea that some people have clear immediate reactions to the gluten itself while other people have kind of silent damage going on and feel bad because of the damage to the GI tract and subsequent poor absorption of nutrients? So if that's the case will the people who don't have obvious immediate reactions to gluten have to be on gluten for longer to notice a decline as well?

Darn210 Enthusiast

It really does depend on the person and the type of issues they have. Many people with digestive issues see improvement pretty quickly. People with nerve damage/neurological symptoms take longer to recover. But it isn't as easy as that . . . my daughter's symptoms looked like digestive issues (regurgitation of food) however, it took about 10 months for symmptoms to disappear. They improved slowly, it was not an all or nothing kind of thing. The theory was that she had nerve damage in her stomach/intestines causing slow motility but it was just a theory.

You certainly don't have to go for as long as six months, but if you are unfamiliar with the diet, you definitely should give yourself some time to be sure that you are following it precisely and then set a time from that point on. When my son was on the trial, my daughter had already been gluten free for about 5 months so I felt like I knew what I was doing diet-wise (not that we still don't have an occasional blunder). I knew by about month 3 that gluten was not an issue for him but my son's doctor wanted 6 months and I was going to make sure that there would be no questioning of the results. Like you said, I didn't want to have to do this again.


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



Celiac.com Sponsor (A8-M):



Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to FannyRD's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Gluten free phosphate binders for dialysis patients

    2. - Scott Adams replied to Cecile's topic in Related Issues & Disorders
      2

      Symptoms

    3. - trents replied to Cecile's topic in Related Issues & Disorders
      2

      Symptoms

    4. - FannyRD posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Gluten free phosphate binders for dialysis patients

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,180
    • Most Online (within 30 mins)
      7,748

    Eldret419
    Newest Member
    Eldret419
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • FannyRD
      Thanks for the resource! I will check it out!
    • Scott Adams
      You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      Living with celiac disease can be especially hard when you’re in a smaller town and don’t have many people around who truly understand it, so you’re definitely not alone in feeling this way. Ongoing fatigue, joint pain, and headaches are unfortunately common in people with celiac disease, even years after diagnosis, and they aren’t always caused by gluten exposure alone. Many people find that issues like low iron, low vitamin D, thyroid problems, other autoimmune conditions, or lingering inflammation can contribute to that deep exhaustion, so it’s reasonable to push your doctor for more thorough blood work beyond just vitamin B. As for eggs, it’s also not unusual for people with celiac disease to develop additional food intolerances over time; tolerating eggs as an ingredient but not on their own can point to sensitivity to the proteins when they’re concentrated. Some people do better avoiding eggs for a while, then carefully testing them again later. Most importantly, trust your body—if something consistently makes you feel awful, it’s okay to avoid it even if it’s technically “allowed.” Many of us have had to advocate hard for ourselves medically, and connecting with other people with celiac disease, even online, can make a huge difference in feeling supported and less isolated.
    • trents
      Welcome to the celiac.com community, @Cecile! It is common for those with celiac disease to develop sensitivity/intolerance to non-gluten containing foods. There is a high incidence of this with particularly with regard to dairy products and oats but soy, eggs and corn are also fairy common offenders. Like you eggs give me problems depending on how they are cooked. I don't do well with them when fried or scrambled but they don't give me an issue when included in baked and cooked food dishes or when poached. I have done some research on this strange phenomenon and it seems that when eggs are cooked with water, there is a hydrolysis process that occurs which alters the egg protein such that it does not trigger the sensitivity/intolerance reaction. Same thing happens when eggs are included in baked goods or other cooked dishes since those recipes provide moisture.  So, let me encourage you to try poaching your eggs when you have them for breakfast. You can buy inexpensive egg poacher devices that make this easy in the microwave. For instance:  https://www.amazon.com/Poacher-Microwave-Nonstick-Specialty-Cookware/dp/B0D72VLFJR/ Crack the eggs into the cups of the poacher and then "spritz" some water on top of them after getting your fingers wet under the faucet. About 1/4 teaspoon on each side seems to work. Sprinkle some salt and pepper on top and then snap the poacher shut. I find that with a 1000 watt microwave, cooking for about 2 minutes or slightly more is about right. I give them about 130 seconds. Fatigue and joint pain are well-established health problems related to celiac disease.  Are you diligent to eat gluten-free? Have you been checked recently for vitamin and mineral deficiencies? Especially iron stores, B12 and D3. Have you had your thyroid enzyme levels checked? Are you taking any vitamin and mineral supplements? If not, you probably should be. Celiac disease is also a nutrient deficiency disease because it reduces the efficiency of nutrient absorption by the small bowel. We routinely recommend celiacs to supplement with a high potency B-complex vitamin, D3, Magnesium glycinate (the "glycinate" is important) and Zinc. Make sure all supplements are gluten-free. Finally, don't rule out other medical problems that may or may be associated with your celiac disease. We celiacs often focus on our celaic disease and assume it is the reason for all other ailments and it may not be. What about chronic fatigue syndrome for instance?
    • FannyRD
      I work as a renal RD and have a Celiac pt which has been rare for me (I might have had 3-4 Celiac pts in 15 years). I wondered if anyone can confirm that these medications are gluten free and safe for Celiac.  Ferric citrate (Auryxia)  Sucroferric oxyhydroxide (Velphoro)  lanthanum carbonate (Fosrenol) sevelamer carbonate (Renvela)   Thank you!
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.