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

New To Gluten-Free


Lfrost

Recommended Posts

Lfrost Explorer

Hi everybody. We are brand new to attempting to eat gluten-free and I have no idea where to start! Let me give you a little background to how we got here.

I have a son who is now 4 years old. We have struggled with constipation and other bowel issues since he was born. He has struggled a lot with potty training, but only with bowel movements. I decided to figure out what was wrong this last year as he would cry while sitting on the toilet that his 'poop was stuck' and beg me to 'get it out' for him. Basically, my son has one bowel movement a day, however, if he misses his daily BM, he becomes constipated.

We ended up at the ER this year because he was so constipated he was crawling around the house crying that his poop was stuck and it hurt, but he couldn't pass it. We talked to our local pharmacist and gave him an over the counter suppository and lots of Miralax. By the afternoon, there was still no change so we took him to the ER. Ironically, while waiting to see the ER doctor, he stopped complaining and crying. My son has a very 'oppositional' temperament and didn't want the doctor to touch him, so he was constantly wiggling around and wouldn't let her feel his belly. Basically, she sent us home and said he was fine. Once we got home, he again went back to crying and crawling around. Finally, he passed the largest stool that I had ever seen come out of a person. I joked with my husband about bringing the stool back to the ER doctor and leaving it for her with a note that said 'not constipated?'

While talking with a friend, she mentioned that milk and other dairy plugs her children up and I should try to take him off of dairy to see. I mentioned it to my doctor and he told me that he didn't believe my son has a milk allergy or intolerance because he would have diarrhea, not constipation. Well, I didn't follow his advice to do nothing, and I removed most dairy from my son's diet. (I say most because we would slip up quite a bit by giving food that might have some cheese or milk in it). But we did take out a lot of the dairy. We switched him to almond milk. Almost immediately the constipation was gone! My son started taking himself to the bathroom instead of hiding and his accidents greatly decreased (from almost daily to about once every other week).

We thought we had it figured out. Well, my son didn't care for the almond milk much (even when adding chocolate syrup to disguise the taste), and slowly steered more towards juices and water. After 3 months of decreasing his dairy, my son started throwing up in the morning. It was strange, he had no fever. His doctor said it was a GI bug that was going around and that it would last about 2 weeks. I didn't really buy it, but a friend at my son's daycare said her daughter was doing the same thing so I guessed he must be right. After 2 weeks of vomiting in the early mornings (usually around 4 am) yet no fever and feeling fine all day, my son got a fever and diarrhea. Again we went to the Dr. who said he must have picked up a new virus because his immune system was down. This was getting old. We were on to 3 weeks of strange GI issues! Interestingly, while the fever was there, the vomiting stopped for a couple of days.

Then the fever was gone and the vomitting was back--early morning, no other signs of sickness. Each day, my son seemed to be getting more and more pale and losing energy. The only change that I could think of in my son's diet was removing dairy. I thought that there must be some connection. We had been on this for 21 days. I went to the Dr. and told him I wanted an allergy test done immediately. We did a blood test and after a few more days, the nurse called and told me my son was not allergic to dairy. That was strange to me, because taking away dairy had 'fixed' the constipation issues. Well, I was ready to try anything, so I immediately gave him a glass of milk and pushed dairy on him for the rest of the day. He loved it. He missed having milk and ice cream, etc.

It was amazing, the vomiting stopped...but the constipation was back. We just had our appointment with our Dr. and he went over the full allergy test results with us. Apparently, my son is allergic to wheat. The Dr. wanted more blood to do a full Celiac panel. We are still waiting for the results from the panel, but in the meantime, I thought I might start focusing on a gluten-free diet.

I have never been one to read labels, and unfortunately, I am not much of a cook. I can cook, I just work all day and haven't been good about making nice homemade meals each night. :(

So, here we are. Brand new to the gluten-free idea, and no idea where to start. I do have 3 older children (ages 15, 13, and 10) who have informed me that they do not want to change their diets because of their brother. Any ideas of where to start? I have no clue what even contains gluten, or not! From reading different posts, I see that things I would have never dreamed of may have gluten in them.

Is there a Dummies Guide to Eating Gluten-Free?!

Sorry for the long post, but if you are still reading this, do you have any suggestions?


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



Celiac.com Sponsor (A8-M):



VydorScope Proficient

So, here we are. Brand new to the gluten-free idea, and no idea where to start. I do have 3 older children (ages 15, 13, and 10) who have informed me that they do not want to change their diets because of their brother. Any ideas of where to start? I have no clue what even contains gluten, or not! From reading different posts, I see that things I would have never dreamed of may have gluten in them.

Is there a Dummies Guide to Eating Gluten-Free?!

Sorry for the long post, but if you are still reading this, do you have any suggestions?

First welcome to the forum! This is a great place to learn form other parents' experiences. Here is some threads to check to get you started:

Some threads with good info:

FAQ Celiac com

https://www.celiac.com/gluten-free/forum-7/announcement-3-frequently-asked-questions-about-celiac-disease/

Celiac Newbie Info 101

What's For Breakfast Today?

What Did You Have For Lunch Today?

What Are You Cooking Tonight?

I know it seems overwhelming right now, but that will pass. In time it will be come just part of your life.

We only have one child, so it is a bit easier on us, others will chime in on how to handle the multi-kid part of this. :)

sa1937 Community Regular

Is there a Dummies Guide to Eating Gluten-Free?!

Welcome to the forum L!

You're in luck...there is an excellent book entitled Living Gluten-Free for Dummies written by Danna Korn.

Jules Shepard also has a good one: The First Year: Celiac Disease and Living Gluten-Free

Sorry, I can't be of any help either on dealing with your other children. Mine are grown with children of their own. But there are a lot of parents on this site, who'll probably be able to give you some good ideas as to how they've handled it.

Lfrost Explorer

You're in luck...there is an excellent book entitled Living Gluten-Free for Dummies written by Danna Korn.

I just found this one and have been reading it all morning! Very informative and helps me realize that others in our family should also be tested! My mother has ulcerative colitis, my oldest two daughters both have ADHD and ADD. Also my oldest has epilepsy which spiked when she was five and has kind of fizzled out. She is also on the autistic spectrum. I didn't realize all of these things can be caused, or at least affected by gluten!

sa1937 Community Regular

I just found this one and have been reading it all morning! Very informative and helps me realize that others in our family should also be tested! My mother has ulcerative colitis, my oldest two daughters both have ADHD and ADD. Also my oldest has epilepsy which spiked when she was five and has kind of fizzled out. She is also on the autistic spectrum. I didn't realize all of these things can be caused, or at least affected by gluten!

Glad you found it...it's an excellent book.

Yes, other family members should also be tested. It's amazing how many symptoms can be attributed to gluten. Check out Open Original Shared Link. First time I saw it, it blew my mind.

Cara in Boston Enthusiast

If you are still waiting for the celiac blood results, DO NOT START THE DIET yet. If the results are positive, the doctor will probably want to perform an endoscopy to determine if there is any damage (he/she may want to do this even if the tests are negative). Changing your diet before the endoscopy can compromise the results. Take this "waiting" time to learn as much as possible about the diet, try some new foods (find acceptable "replacement" foods) etc.

After testing is done, then start the diet. Hopefully you won't have to wait long since you have already been told he has a wheat allergy.

Yes, everyone in the family should also be tested.

Cara

Kelleybean Enthusiast

I know it seems so overwhelming at first! This board has been incredibly helpful to me. I have a 4 year old too and I know how picky they can be! Couple of things that he likes: Udi's bread (sometimes I do a "grilled cheese" using Better than Cream Cheese in the middle - it's dairy free), chocolate chip cookies with the recipe from Elana's Pantry website, the banana bread from Spunky Coconut cookbook, Envirokids Cereals, Van's Waffles, Applegate Farms hotdogs, and Ian's alphabet fries. I believe Applegate Farms also has some gluten free chicken nuggets. We also do a recipe with Namaste muffin mix where I sneak in some pureed veggies and mashed beans for protein. There are probably a lot of things that you make for him already that are either naturally gluten free or can be easily made gluten free by some simple substitutions (like using gluten free bread crumbs for regular).

If you have some time, and it sounds like you do if you decide to wait for the test results, then you can play with some recipes and products. Then if you have to make the switch you won't be starting from scratch. Because my son is on the gluten free diet because of autism and not celiac, we had the luxury of taking our time and experimenting.


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.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,946
    • Most Online (within 30 mins)
      7,748

    Miva
    Newest Member
    Miva
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • 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.