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

Probiotics? Other Supplements For Kids?


Christine0125

Recommended Posts

Christine0125 Contributor

Anyone give their kids probiotics or other supplements to help? 

 

A little background: My almost 10 year old was diagnosed with celiac last December.  The first few months were great gluten-free but lately she's been having tummy ups and downs (she's at the too embarrassed to share bathroom issues with me phase).  I started her on gummy probiotics a few weeks back and it really seemed to help so I thought I'd found the solution to keeping her regular but now it seems the issues are back. 

 

Any tips and tricks from parents out there as to what helps keep your celiac kids feeling well?  We plan to keep a food log to see if there is another obvious trigger that we haven't clued into.  95% of the time we eat at home in a completely gluten free kitchen.  When we eat out, I'm also celiac so we eat the same thing and I've not felt any obvious signs of gluttening (although I know she may be more sensitive than me). 

 

So hard to figure out when she's at an age where if I push her to share too much then she shuts down completely so I feel I'm walking a thin line trying to figure things out.  I do have her onboard with the casual "hey, lets just experiment with the things you eat a bit so we can make sure you feel good all the time." 


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



Celiac.com Sponsor (A8-M):



Rosiesallergies Rookie

Has the doctor looked at any other food sensitivities? Milk/casein is frequently a problem for kids. My child couldn't eat dairy for years after going gluten-free.

Another thought is school environment. Is your child getting contaminated at school? Lunch room is the obvious place. What about food based learning? Art class? Teacher rewards like candy?

Does your child bite their nails? Or possibly not wash their hands well enough before eating?

Good luck finding the source of the problem.

GF Lover Rising Star

It does sound like she is still getting gluten.  Most likely at school.  And I'm assuming she is in school and not home schooled.   When your first diagnosed, the motivation is great to comply with the diet because the reward is immediate, feels better.  Then she's out for summer vacation, the diet is still going well, Mom is still making food decisions.  Now School has started up. Maybe she is making mistakes at school, feeling pressure from peers, cross contamination.   And of course, another intolerance is possible.  I wouldn't start supplementing with vitamins unless she is actually deficient.  I think a pro-biotic is fine.

 

Colleen

Christine0125 Contributor

She very well could be getting cross-contaminated at the lunch table although she purposely requests no nuts in her lunch so she can eat at the less crowded peanut-free table.  We did a 504 plan for her which I could update to have her sit separately although that's a tough call based on the social aspect of elementary school. 

 

I'm certain she's not experimenting due to peer pressure (not that type of kid at all).  I do likely need to explore dairy or other intolerances more... hence that food log that I've been talking of starting but haven't yet done.  I've seen apps for that, anyone use one?  Maybe I'll ask that on one of the general boards. 

 

Thanks for your input!

GF Lover Rising Star

Yea, I don't think I would have her sit separately.  Although I wonder if she is getting cross-contaminated with her school lunch.  It is prepared in the same kitchen at school?  Or do you pack her lunch?  Otherwise, like you said, look for other intolerances.  Dairy would be the first to try.  I don't know of any apps.

 

Colleen

Mizzo Enthusiast

If you have the option of volunteering for lunch duty for 1 or 2 days, that can give you the insight you need regarding cross contamination at lunch. My DD is 10 and in 5th grade and they have switch classes. If your girl has the same make sure the switch desk is being wiped down after snack time. Also a snack/lunch mat brought from home will dramatically cut down on CC issue's. 

 

Keep up the food diary for a while you may notice a trigger like dairy, soy, oats or corn. Probiotics are a good idea. My DD has multivitamins,Omega 3 and Fiber gummies everyday. We are 3 1/2 yrs gluten-free and she still has constipation issue's with the opposite happening when we use Miralax, and with the added DX this year of Hashimota's disease there is always something. My girl doesn't eat veggies so until that changes for us, it will always be like this.  

 

good luck

greenbeanie Enthusiast

My daughter is four and was just diagnosed in June, and for the first couple months I gave her probiotics every day. We used Go Live flavorless powder packets from Whole Foods, mixed with juice. It seemed to make a really big difference at first, and on the occasional day when we'd run out or I'd forget she'd have almost-diarrhea, like she did before diagnosis.

After a couple months I started giving her the probiotics a few times a week instead of every day, and this was also a time when her general behavior and mood started to decline again. At first I thought she must be getting glutened at pre-school (which had just started), though they are extremely careful about cc and all art supplies and snacks served there are now gluten free. Then I thought that maybe the decline was just due to being overtired and not napping at school. And maybe it was one or the other of those things - I'm really not sure. But somewhere along the line I realized that I'd also reduced the probiotics around the same time, so I resumed giving them to her daily. Within two days, she was on the upswing again! Maybe it was a coincidence, but I'm not planning to stop again anytime soon. A nutritionist at her GI's office had recommended either yogurt or probiotic supplements every day for a while after diagnosis (she didn't say how long), so we're going to stick with them for at least a few more months. Good-quality probiotics sure are expensive, though!


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



Celiac.com Sponsor (A8-M):



  • 2 weeks later...
ImaMiriam Apprentice

Probiotics seem very complicated to me. I took my 12 year old daughter to a nutritionist on Saturday, and she said that one should only take probiotics for a short period of time, for example, for 2-3 weeks after being on an antibiotic. My daughter was taking 2 different probiotics which the pediatric GI had proscribed, and my daughter was continuing to have stomach aches. The nutritionist said she thought the stomach aches might be from the probiotics.

 

We're now off the probiotics and totally off dairy. We'll be off dairy for 1-3 weeks and see what happens. If all stomach symptoms go away, then we'll start dairy really really slowly - the nutritionist gave us a way to gradually add back the dairy foods, starting with the ones that are most easily tolerated.

 

We're also keeping a food diary. Here's what to put in your diary -- meal, time of day, location, amounts of the foods you eat, and any pain. I'm already finding this diary helpful to look at. I think including all of these details are really important. We'd tried a diary before and didn't put amounts and also didn't write down if there was any pain...

 

My daughter also had some blood tests for vitamin levels and so on. I think these are a good idea if they help you see what's going on. If your child is constipated frequently and/or diarrhea frequently, other issues will possibly creep in such as anemia...important to watch out for this.

 

Good luck!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,545
    • Most Online (within 30 mins)
      7,748

    Jem68
    Newest Member
    Jem68
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.