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

HELP!


Tracey

New and need help  

3 members have voted

You do not have permission to vote in this poll, or see the poll results. Please sign in or register to vote in this poll.

Recommended Posts

Tracey Newbie

Help! My 4 1/2 yr old son WITH DOWN SYNDROME has somewhat been diagnosed with Celiac Disease...I think. He's been having a lot of sinus infections this past year and his Dr did a recent allergy test. I've just recieved a call from the Dr's office saying he's mildly allergic to wheat and corn and they have mailed me a list of what is acceptable and what is not. The diet is for people with celiac disease. I will not be able to confirm this with the dr's office until Monday so that's why I'm unsure about this. I am aware that Celiac disease is pretty common in people with Down Syndrome. My question is this....where do I begin? I'm overwhelmed! Everything in my house countains gluten I think! I also have a 13 yr old and a 2 yr old so I'm not going to be able to let them eat what Jacob likes and can't have in front of him. That would be cruel!!! Any suggestions from the pros??? Where do you get the special food products? Any helpful advice would be soooo appreciated.

Thanks in advance,

Tracey


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



Celiac.com Sponsor (A8-M):



lauradawn Explorer

Hi Tracey,

Im not an expert at this.........yet. I was just recently diagnosed with celiac disease ( blood work) and b/c my children (2 year old twins ) have had some significant health issues since they were born, I decided to have them tested as well. I have recieved the results from the blood work, but have not seen the Dr until Wed. I do know that it looks like they are positive as well, so I am doing the same thing you are. Going through the pantries. When it was just myself...I made my own pantry of things that were gluten-free. However, now that my kids are both likely to be celiac, my plan is to make my house gluten-free. IF my husband really wants to although he is very supportive, he could have his own cupboard. Depending on what the Dr says you may want to check your other kids out too. Celiac is a genetic disease. If your son has it your others may have or possibly have it in the future. Something to consider.

I buy my special flours from the health food store. For the most part everything else I can by from the grocery store. I know it seems overwhelming at first, but the shopping part and finding appropriate foods is not that difficult. There are some product listsings on the web, that can help you find just about any kind of food, you just have to find the right brand. Take one step at a time, and the people here are great! Just hang in there. Im still in that waiting process to, but you may find that your sons health issues improve. It's worth the inconvience Im sure.

Please let us know

Laura

Terri-Anne Apprentice

:) Hi Tracey,

My son is 4 years old and has a rather sensitive wheat allergy, but does not have celiac disease, according to our pediatrician. We've been attempting to keep him wheat-free for approximately 2 years now, though I still wouldn't consider myself an expert. I learn something new all the time.

I know it can be very overwhelming to try to keep wheat out of the diet at first, as when you read labels it seems EVERYTHING in your entire pantry has wheat as a staple or supporting ingredient. You've come to the right place though. The people at this web site are very friendly, experienced, knowledgeable and helpful!

My first piece of advice would be to keep coming here, on an on-going basis.

My second piece of advice is to get into contact with your nearest local chapter of a Celiac support group. They are good for letting you know specifically what products are available in YOUR area, as well as which ones could be substituted for those that aren't available in your area.

It would be important to know whether your son has actual celiac, or a wheat allergy, as with the wheat allergy alone, the diet can be slightly (though not amazingly) more liberal. For example, my son can eat regular Rice Krispies, which folks with celiac must avoid, because of the barley malt in the ingredients. For the most part though the wheat-free diet is very, very similar to the celiac diet, as wheat is still the main offender. That's why learning from people experienced with celiac is the best.

As for your son having to stand by and watch the other kids eat things he cannot have, Once you catch on to a few products which he likes and can have, he will likely accept substitutions well. Many things can be substituted exactly, for example, Logan loves rice crackers with cheese or peanut butter when the others eat Ritz crackers with cheese/peanut butter. He knows that the crackers the others are eating are "wheat" crackers which make him feel yucky, but his yummy rice crackers won't make him feel sick, AND I think he gets somewhat of a kick that the others can't have HIS crackers, they are exclusively HIS. THEY think it is a special treat when they are allowed to have some of HIS special foods. Before I went shopping yesterday to restock his own wheat free pantry, I had nothing for his breakfast, so I let him have a can of Campbell's chicken and Rice soup for breakfast. He thought that was neat.

One of the first things that I was mortified that Logan wouldn't be able to have was pasta, as he loved pasta. My local celiac group suggested the Tinkyada brand pasta made with rice flour, and told me exactly where to buy it locally. We discovered the cooking time is slightly longer, but the cooked pasta is almost identical to the wheat flour type.

Do you bake? I've just finished baking a batch of banana chocolate chip muffins for Logan using a combination of rice flour/potatoe starch/tapioca flour, and guar gum (which replaces the stickiness of gluten), and have two loaves of bread in the oven for him for the week ahead. I have some cupcakes I made for him in the freezer, as well as a few brownies. His own pantry has a bag of Mi-Del brand chocolate chip cookies, Mi-Del oreo style cookies, and he just finished his Mi-Del animal crackers off yesterday.

We try to keep the "tempting" wheat products like cookies, up high in our "WHEAT PANTRY", but his safe rice flour cookies are reachable in a pantry in the opposite side of the room. He still needs to ask permission before having a treat, but if he happens to sneak as kids sometimes do, he usually gets into a wheat-free snack. At least that way his appetite may be ruined, but he won't have a reaction, which are pretty dramatic.

I wish you luck in your new adventure with providing your son with a wheat free diet. Come here often, and ask plenty of questions. The folks here really are a wonderful support network. If you'd like I could share a couple of basic recipes, brands of soup, treats, etc. with you, as my son is also wheat free, (to the best of our ability).

Oh yeah, and the Dana Korn book "Raising Our Celiac Kids" is also a great resource.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,960
    • Most Online (within 30 mins)
      7,748

    Noa
    Newest Member
    Noa
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • 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
×
×
  • 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.